Natural terpenoids with therapeutic potential against pulmonary arterial hypertension

Pulmonary arterial hypertension (PAH) is a devastating disorder characterized by progressive pulmonary vascular remodeling, chronic inflammation, and right heart failure. Current vasodilation-focused therapeutic strategies often fail to reverse established vascular structural lesions and inadequately control disease progression. Natural terpenoids demonstrate significant anti-remodeling potential through their structural diversity and multi-target intervention capabilities, including suppression of oxidative stress, blockade of inflammatory pathways, regulation of endothelial-mesenchymal transition (EndMT), restoration of the cellular proliferation/apoptosis balance, and recovery of ion channel functionality. This review systematically summarizes the pharmacological effects, molecular mechanisms, and limitations of natural terpenoids in ameliorating PAH, providing novel perspectives for targeted therapies. To advance clinical translation, future efforts must prioritize large-scale trials validating safety profiles and optimizing dosing regimens, while diversifying natural sources to accelerate precision drug development.

1 Introduction

Pulmonary arterial hypertension (PAH) is a progressive and highly lethal cardiopulmonary disorder characterized by sustained elevation of pulmonary arterial pressure (PAP) and pulmonary vascular resistance (PVR), primarily resulting from abnormal pulmonary vascular remodeling and excessive proliferation of pulmonary arterial smooth muscle cells (PASMCs) (Zhang et al., 2024a). This pathological process subsequently leads to right ventricular hypertrophy (RVH), RV diastolic and systolic dysfunction, and ultimately right heart failure, which severely threatens patient survival (Yu Z. et al., 2022). Epidemiological data indicate that despite advances in clinical diagnosis and treatment, the long-term prognosis of PAH remains poor, with a 5-year mortality rate exceeding 40% in many patient cohorts (Langleben et al., 2022).

Currently, the mainstay of PAH management relies on pharmacological interventions such as endothelin receptor antagonists, phosphodiesterase-5 inhibitors, and prostacyclin analogs, which primarily target vasodilation (Langleben et al., 2022; Zhang et al., 2024b). However, these drugs offer only symptomatic relief, without fundamentally reversing the underlying vascular pathological remodeling or halting disease progression. Moreover, their long-term administration is frequently associated with adverse effects, high treatment costs, and limited accessibility in low-resource settings. Consequently, the development of safer, more effective, and mechanism-oriented therapeutic strategies has become an urgent focus in the field of PAH research.

Natural terpenoids, a diverse class of secondary metabolites widely distributed in plants, possess a broad spectrum of pharmacological properties, including antioxidant, anti-inflammatory, vasodilatory, and cardiovascular protective effects (Oliveira et al., 2021; Abdul Ghani et al., 2023). Recent experimental studies have highlighted their potential role in PAH prevention and treatment through multiple mechanisms, such as inhibiting pulmonary vascular remodeling, suppressing excessive PASMCs proliferation, reducing oxidative stress, and modulating apoptosis (Silva et al., 2021). Notably, certain monoterpenes have demonstrated the ability not only to lower pulmonary arterial pressure but also to improve endothelial function via regulation of ion channel activity, thereby reducing PVR and alleviating the hemodynamic burden in PAH (Silva et al., 2021; Zeng et al., 2023).

Emerging preclinical evidence further supports this therapeutic potential: for instance, 4-terpineol has been shown to mitigate hypoxia-induced pulmonary arterial remodeling in PAH rat models (Gu et al., 2023), while perillyl alcohol administration has produced favorable hemodynamic improvements in experimental PAH (Beik et al., 2021). At the molecular level, terpenoids may suppress abnormal PASMC proliferation by regulating mitochondrial function, ion channel dynamics, and specific signaling pathways, such as downregulating the 12-lipoxygenase/12-hydroxyeicosatetraenoic acid axis, thereby significantly reducing PVR and improving hemodynamic parameters (Zhang C. et al., 2018; Ruffenach et al., 2024; Wang et al., 2025).

In summary, accumulating evidence suggests that natural terpenoids not only have the potential to serve as adjuvant therapies complementing existing pharmacological regimens but may also emerge as promising frontline agents for early intervention in PAH, offering the dual advantages of minimizing adverse effects and improving long-term prognosis (Oliveira et al., 2021). Based on this rationale, the present review aims to comprehensively summarize recent advances in terpenoid-based research for PAH prevention and treatment, with a particular emphasis on their underlying mechanisms of action, targeted signaling pathways, and translational potential, thereby providing a robust theoretical framework and scientific basis for the development of novel, personalized therapeutic strategies in PAH.

2 Methods

The literature for this review was retrieved from PubMed, ScienceDirect, Web of Science, and Google Scholar databases, covering publications up to September 2025 and restricted to English-language sources. The search strategy employed the terms “pulmonary arterial hypertension,” “natural products,” “terpenoids,” and “terpenes,” as well as various combinations of these keywords. Approximately 160 relevant publications, comprising both original research and reviews, were selected for this analysis.

3 Classification and pharmacological activities of natural terpenoids

3.1 Classification of natural terpenoids

Terpenoids constitute a vast and diverse class of naturally occurring organic compounds, ubiquitously distributed throughout the plant kingdom (Johnson et al., 2023; Hoshino and Villanueva, 2023). Their fundamental structural framework is built upon the isoprene unit, a five-carbon building block, as depicted in Figure 1 (El-Baba et al., 2021). As integral products of plant secondary metabolism, terpenoids are especially abundant in the essential oils of aromatic plants, where they contribute not only to fragrance but also to ecological interactions and defense mechanisms (Mathur et al., 2024). Depending on the number of isoprene units incorporated into their carbon skeleton, these compounds are classified into distinct subclasses, including monoterpenoids, sesquiterpenoids, diterpenoids, triterpenoids, and tetraterpenoids (Burger et al., 2021). In the present article, we provide a systematic overview of naturally derived terpenoids with potential applications in the prevention and treatment of pulmonary arterial hypertension (PAH), with representative molecular structures illustrated in Figure 2.

Figure 1

Figure 1. Chemical structural formula of isoprene.

Figure 2

Figure 2. Representative natural terpenoid compounds for the treatment of PAH.

3.2 Pharmacological activities of natural terpenoids

As structurally diverse and functionally versatile secondary metabolites of plants, natural terpenoids have attracted considerable attention for their pharmacological potential in the prevention and treatment of cardiovascular diseases, particularly PAH. Accumulating evidence demonstrates that terpenoids exert a broad spectrum of bioactivities, including potent anti-inflammatory and antioxidant effects, suppression of vascular remodeling, and regulation of vascular smooth muscle cell and endothelial cell proliferation and apoptosis. Moreover, they can inhibit the persistent activation of multiple aberrant signaling pathways associated with PAH pathogenesis. Certain terpenoids are also capable of attenuating endothelial-to-mesenchymal transition (EndMT), thereby contributing to the preservation of vascular structural integrity and the restoration of endothelial function. Through these pharmacological actions, terpenoids provide multi-target and multi-pathway therapeutic strategies aimed at delaying, or potentially reversing, the pathological progression of PAH. In this review, we compile and critically assess 23 representative natural terpenoids reported to be effective in PAH prevention and treatment. Their botanical sources, molecular targets, principal signaling pathways, and major pharmacological effects are systematically summarized and comparatively analyzed, with detailed information presented in Table 1.

Table 1

Table 1. Mechanisms of natural terpenoids in the treatment of PAH.

3.2.1 Monoterpenoids

3.2.1.1 D-Limonene

D-Limonene is a naturally occurring monocyclic monoterpene predominantly present in the peels and essential oils of Citrus sinensis (L.) Osbeck (Fam. Rutaceae) (Anandakumar et al., 2021; Rakoczy et al., 2025). The pathological progression of PAH is intimately linked to sustained inflammatory responses and oxidative stress, both of which drive pulmonary vascular remodeling and ultimately result in right ventricular (RV) dysfunction (Igarashi-Sugimoto et al., 2025). Experimental studies have demonstrated that D-limonene exerts potent anti-inflammatory and antioxidant effects—pharmacological properties of particular relevance to the vascular pathological microenvironment of PAH (Hou et al., 2022; Teixeira-Fonseca et al., 2024). At the molecular level, D-limonene downregulates the mitogen-activated protein kinase (MAPK) signaling pathway and the expression of the pro-apoptotic gene B-cell lymphoma 2-associated X protein (Bax), while upregulating the anti-apoptotic gene B-cell lymphoma 2 (Bcl-2), thereby suppressing cardiomyocyte apoptosis (Wang et al., 2018b; Younis, 2020). Such activity may mitigate PAH-induced cardiomyocyte loss and provide indirect protection for RV function, considering that right heart failure remains one of the most common and fatal outcomes of advanced PAH. In addition, D-limonene has been shown to attenuate ischemia-related vascular injury by inhibiting pathological vascular remodeling and enhancing antioxidant defenses, thereby partially restoring vascular homeostasis under PAH conditions (Wang et al., 2018b; Anandakumar et al., 2021).

3.2.1.2 Paeoniflorin

Paeoniflorin is a monoterpene glycoside primarily isolated from the dried roots of Paeonia lactiflora Pall. (Paeoniaceae) (Li et al., 2023). In rat models of PAH, paeoniflorin has been shown to mitigate pulmonary tissue injury, alleviate PAH symptoms, and markedly improve survival rates by reversing EndMT associated with bone morphogenetic protein receptor type II (BMPR2) downregulation (Yu et al., 2020; Cao et al., 2025). Subsequent investigations have demonstrated that paeoniflorin significantly decreases the levels of multiple fibrosis-related markers in lung tissue, including collagen type IV, α-smooth muscle actin (α-SMA), hyaluronic acid, laminin, and procollagen type III (Yu M. et al., 2022). Moreover, it suppresses the expression of collagen types I and III, thereby effectively attenuating pulmonary vascular remodeling. These anti-fibrotic actions, together with its ability to inhibit inflammatory responses, underscore the potential of paeoniflorin as a multi-target therapeutic agent for delaying or halting the pathological progression of PAH (Yu et al., 2021).

3.2.1.3 Perillyl alcohol

Perillyl alcohol is a naturally occurring monoterpene alcohol widely distributed in the essential oils of various plants, including Perilla frutescens (L.) Britton, Lavandula angustifolia Mill., and Mentha × piperita L. (Fam. Lamiaceae) (Zhang L. et al., 2024). Derived primarily from plant volatile oils, it is characterized by a distinctive aromatic fragrance (Chen et al., 2021). Evidence from experimental animal studies demonstrates that perillyl alcohol can dose-dependently and significantly ameliorate the symptoms of PAH by reducing pulmonary arterial pressure, attenuating RVH, and inhibiting pulmonary vascular remodeling (Rajabi et al., 2020; Beik et al., 2021; Kordestani et al., 2024). At the molecular level, it modulates the expression of multiple microRNAs and inhibits the activity of poly(ADP-ribose) polymerase 1 (PARP1), thereby reducing oxidative stress and suppressing aberrant cell proliferation (Rajabi et al., 2020; Puppala et al., 2022). In addition, perillyl alcohol inhibits farnesyltransferase, which regulates inflammation-related signaling pathways and confers synergistic anti-inflammatory and antioxidant effects (Puppala et al., 2022).

3.2.1.4 1,8-Cineole

1,8-Cineole is a major monoterpene oxide abundantly present in the volatile oils of various aromatic plants, particularly Eucalyptus globulus Labill. (Myrtaceae) and Salvia rosmarinus Spenn (Lamiaceae; syn. Rosmarinus officinalis L.) (Pereira-Gonçalves et al., 2018). In the context of PAH, 1,8-cineole exerts protective effects by modulating the dysregulated BMPR2/Smad1/5 and BMPR2/PPAR-γ signaling pathways, thereby inhibiting pulmonary vascular remodeling (Alves-Silva et al., 2025). These actions result in reduced collagen deposition within lung tissue, suppression of excessive vascular smooth muscle cell proliferation, and attenuation of medial layer thickening in pulmonary arteries (Alves-Silva et al., 2025). With respect to oxidative stress, 1,8-cineole significantly decreases the levels of reactive oxygen species (ROS), malondialdehyde (MDA), and lipid peroxides (LPO), while enhancing the enzymatic activities of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), and catalase (CAT) (Chen et al., 2023; Liu Z. et al., 2023). In terms of immune and inflammatory regulation, it has been shown to inhibit the release of pro-inflammatory cytokines, including tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IL-4, and IL-5, and to restore Th1/Th2 immune balance (Juergens et al., 2020). Furthermore, 1,8-cineole exhibits antihypertensive activity primarily through the inhibition of calcium (Ca²⁺) channels in vascular smooth muscle cells, leading to reduced vascular tone (Pereira-Gonçalves et al., 2018; Nozohour et al., 2022). In PAH, this vasodilatory effect may directly alleviate pulmonary vasoconstriction, thereby improving hemodynamic status and potentially relieving RV strain (Pereira-Gonçalves et al., 2018; Alves-Silva et al., 2022).

3.2.1.5 Carvacrol

Carvacrol is a phenolic monoterpenoid abundantly distributed in the essential oils of aromatic herbs of the family Lamiaceae, such as Origanum vulgare L., Thymus vulgaris L., and Satureja hortensis L. (Singh et al., 2023). In ex vivo rat aortic ring assays, carvacrol has been shown to elicit a pronounced vasorelaxant response, while in vivo studies confirm its antihypertensive activity (Testai et al., 2016). In terms of antioxidant and anti-inflammatory properties, carvacrol effectively mitigates oxidative stress, suppresses the release of the pro-inflammatory cytokine IL-1β, and enhances the secretion of the anti-inflammatory cytokine interleukin-10 (IL-10) (Zhang et al., 2016; Khazdair et al., 2024; Koçak et al., 2025). At the molecular level, carvacrol inhibits the MAPK signaling pathway and blocks the activity of the transient receptor potential melastatin 7 (TRPM7) channel, thereby disrupting proliferation-related signaling cascades and attenuating pulmonary vascular remodeling (Cai et al., 2021).

3.2.2 Sesquiterpenoids

3.2.2.1 Curcumol

Curcumol is a bioactive sesquiterpenoid extracted from the essential oil of the rhizomes of Curcuma phaeocaulis Valeton (Fam. Zingiberaceae) (Zhai et al., 2024). In vitro studies have shown that curcumol effectively inhibits EndMT in primary rat pulmonary artery endothelial cells (PAECs) induced by TNF-α, transforming growth factor-β1 (TGF-β1), and interleukin-1β (IL-1β) (Nie et al., 2023). In a monocrotaline (MCT)-induced rat model of PAH, curcumol attenuated RVH and reduced pulmonary arterial wall thickening in a dose-dependent manner, thereby exerting a significant protective effect against pulmonary vascular remodeling (Nie et al., 2023).

3.2.2.2 Parthenolide

Parthenolide, a sesquiterpene lactone predominantly obtained from Tanacetum parthenium (L.) Sch.Bip. (Fam. Asteraceae), has demonstrated notable pharmacological potential in PAH (Freund et al., 2020). In vitro studies reveal that parthenolide inhibits hypoxia-induced proliferation and migration of PASMCs while promoting their apoptosis (Yao et al., 2024). Mechanistically, parthenolide directly interacts with signal transducer and activator of transcription 3 (STAT3), markedly reducing its phosphorylation and nuclear translocation, thereby suppressing downstream pro-proliferative signaling cascades (Yao et al., 2024). In vivo, administration of parthenolide significantly decreased mean pulmonary arterial pressure (mPAP), attenuated pulmonary vascular remodeling, and reduced collagen deposition, highlighting its potential as a therapeutic agent for slowing or preventing PAH progression (Yao et al., 2024).

3.2.2.3 Fumagillin

Fumagillin is a secondary metabolite produced through the fermentation of the fungus Aspergillus fumigatus Fresen (Ingber et al., 1990). Experimental studies have shown that fumagillin markedly reduces the infiltration of CD45⁺ immune cells into lung tissue, thereby alleviating inflammatory responses (Kass et al., 2012). At the molecular level, fumagillin inhibits the enzymatic activity of methionine aminopeptidase-2 (MetAP2), which in turn blocks platelet-derived growth factor (PDGF)-driven proliferation of smooth muscle cells, ultimately suppressing pulmonary vascular remodeling (Kass et al., 2012). Owing to this combination of anti-inflammatory and anti-proliferative effects, fumagillin holds potential as a multi-target therapeutic candidate for the prevention and treatment of PAH.

3.2.3 Diterpenoids

3.2.3.1 Tanshinone IIA

Tanshinone IIA, a major lipophilic diterpene quinone isolated from the phytomedicine Salvia miltiorrhiza Bunge (Danshen), is predominantly concentrated in its roots and rhizomes (Guo et al., 2020). Experimental studies have demonstrated that tanshinone IIA can suppress hypoxia-induced pulmonary vascular structural abnormalities, thereby attenuating the severity of PAH (Zhang N. et al., 2018; Li et al., 2022b). Mechanistically, tanshinone IIA inhibits the aberrant proliferation of PASMCs under hypoxic conditions by modulating the Protein kinase B (Akt)/S-phase kinase-associated protein 2 (Skp2)/Cyclin-dependent kinase inhibitor 1B (p27) signaling pathway (Luo et al., 2013). It also reduces the release of pro-inflammatory cytokines, including TNF-α, IL-1β, and interleukin-6 (IL-6), thereby attenuating pulmonary inflammation (Fu et al., 2021; Yang L. et al., 2021). From an antioxidant perspective, tanshinone IIA activates the nuclear factor erythroid 2-related factor 2 (Nrf2) pathway, enhancing the activities of SOD and CAT while reducing lipid peroxide accumulation, thus preventing oxidative stress-induced cellular injury (Gu et al., 2016; Fu et al., 2021; Wu M. et al., 2024). Moreover, tanshinone IIA exerts multi-target vascular protective effects by regulating both Ca²⁺ and K⁺ channel activities, significantly improving vascular dysfunction in hypoxic PAH (Wang et al., 2010). Notably, its water-soluble derivative, sodium tanshinone IIA sulfonate, has been shown in animal studies to inhibit the MAPK signaling pathway, thereby reducing oxidative stress damage and mitigating pulmonary vascular remodeling (Bao et al., 2020; Xu et al., 2025).

3.2.3.2 Crocin

Crocin, a naturally occurring carotenoid glycoside isolated from saffron (Crocus sativus L.), exhibits potent anti-inflammatory and antioxidant activities that underpin its diverse pharmacological effects (Sheng et al., 2022; Xi et al., 2025). In terms of inflammation regulation, crocin downregulates the C-C motif chemokine ligand 2/C-C chemokine receptor 2 (CCL2/CCR2) signaling pathway, thereby reducing pulmonary levels of pro-inflammatory cytokines such as TNF-α and IL-6 (Sheng et al., 2022). With respect to oxidative stress, crocin effectively mitigates ROS-induced pulmonary vascular injury, alleviating oxidative burden and preventing further tissue damage (Dianat et al., 2020; Sheng et al., 2022). From a hemodynamic perspective, crocin significantly decreases right ventricular systolic pressure (RVSP) and mPAP, thereby reducing RV afterload. It also inhibits the abnormal proliferation of PASMCs, attenuates pulmonary vascular wall thickening, and suppresses fibrotic processes, effectively reversing pulmonary vascular remodeling (Sheng et al., 2022). Additionally, crocin restores the balance between matrix metalloproteinase-2 (MMP-2) and tissue inhibitor of metalloproteinase-1 (TIMP-1), contributing to the maintenance of pulmonary vascular structural homeostasis (Deng et al., 2024).

3.2.3.3 Andrographolide

Andrographolide, the major bioactive constituent extracted from Andrographis paniculata (Burm.f.) Wall. ex Nees (Fam. Acanthaceae), is widely recognized for its therapeutic use in the treatment of inflammation, infections, and cardiovascular diseases (Hsu et al., 2016; Wong et al., 2021). Studies have demonstrated that andrographolide significantly alleviates pulmonary inflammation and oxidative stress associated with PAH by suppressing the expression of pro-inflammatory factors TNF-α, IL-1β, C-X-C motif chemokine ligand 1 (CXCL1), and the oxidative damage marker 8-hydroxy-2′-deoxyguanosine, thereby improving PAH-related pulmonary vascular remodeling (Wu et al., 2017; Tran et al., 2021; Liu B. et al., 2022). Animal studies have further confirmed that this compound markedly reduces collagen deposition and inflammatory cell infiltration in lung tissue (Tan et al., 2016; Karkale et al., 2018). With respect to cardioprotection, andrographolide can improve PAH-induced ventricular remodeling and cardiac dysfunction by blocking the MAPK signaling pathway (Wu et al., 2017; Othman and Mohd Azman, 2022; Tian et al., 2023). Moreover, it modulates the abnormal proliferation and apoptosis of PASMCs and endothelial cells, thus inhibiting pathological vascular structural alterations at a multicellular level (Nie et al., 2021; Han et al., 2023; Shan et al., 2025).

3.2.3.4 Triptolide

Triptolide, a highly bioactive diterpenoid triepoxide isolated from the phytomedicine Tripterygium wilfordii Hook.f. (Fam. Celastraceae), possesses potent anti-inflammatory, immunosuppressive, and anti-proliferative properties (Zhang et al., 2020). In vivo studies have demonstrated that triptolide markedly alleviates MCT or pneumonectomy-induced PAH and the associated RVH by inhibiting pathological cell proliferation, suppressing inflammatory responses, and improving pulmonary vascular remodeling (Wei et al., 2007a). Moreover, triptolide not only slows PAH progression but can also partially reverse established vascular remodeling by inhibiting the activities of MMP-2 and matrix metalloproteinase-2 (MMP-9), thereby contributing to the downregulation of pulmonary inflammation (Wei et al., 2007b).

3.2.3.5 Oridonin

Oridonin, a bioactive ent-kaurane diterpenoid isolated from the phytomedicine Isodon rubescens (Hemsl.) H.Hara (syn. Rabdosia rubescens), exhibits a wide range of pharmacological activities, notably anti-inflammatory and antioxidant effects (Li et al., 2021; Gao et al., 2022; Yang et al., 2022). In rat models of PAH, oridonin has been shown to attenuate and even reverse disease progression by concomitantly modulating the nuclear factor-κB (NF-κB) and extracellular signal-regulated kinase (ERK) signaling pathways, thereby effectively suppressing inflammatory responses and alleviating oxidative stress (Wang et al., 2009).

3.2.4 Triterpenoids

3.2.4.1 Ginsenoside Rb1

Ginsenoside Rb1, a major protopanaxadiol-type saponin predominantly distributed in the roots of Panax ginseng C.A. Mey. and Panax notoginseng (Burkill) F.H. Chen ex C.Y. Wu and K.M. Feng (Fam. Araliaceae), exerts diverse pharmacological activities, including anti-inflammatory, antioxidant, anti-fibrotic, and cardiovascular protective effects (Gong et al., 2022; Liu J. et al., 2022). In the context of PAH, ginsenoside Rb1 has been shown to effectively lower PVR by inhibiting the activity of store-operated calcium entry (SOCE) channels, thereby reducing excessive pulmonary vasoconstriction (Wang R.-X. et al., 2015; Wang R.-X. et al., 2020).

3.2.4.2 Ginsenoside Rg1

Ginsenoside Rg1, a major protopanaxatriol-type saponin predominantly derived from Panax ginseng and Panax notoginseng, exhibits multiple protective effects on the pulmonary vasculature (Wu J.-J. et al., 2024). In the context of PAH, ginsenoside Rg1 attenuates vascular inflammatory responses by downregulating the senescence-associated markers cyclin-dependent kinase inhibitor 1A (p21) and cyclin-dependent kinase inhibitor 2A (p16), thereby suppressing the cyclic GMP-AMP synthase/stimulator of interferon genes (cGAS/STING) signaling pathway (Ding et al., 2025). In addition, ginsenoside Rg1 upregulates the expression of cellular communication network factor 1 (CCN1), which in turn inhibits the TGF-β1/p-Smad2/3 signaling axis, effectively reversing hypoxia-induced endothelial dysfunction (Tang B.-L. et al., 2023). At the smooth muscle cell level, it suppresses the calpain pathway, thereby ameliorating abnormal hypoxia-driven proliferation of PASMCs (Ran et al., 2024). Furthermore, ginsenoside Rg1 reduces ROS generation and intracellular Ca²⁺ concentration in human pulmonary microvascular endothelial cells, while enhancing mitochondrial function and energy metabolism, thus preserving endothelial homeostasis (Chen et al., 2024).

3.2.4.3 Ginsenoside Compound K

Ginsenoside Compound K, a rare secondary metabolite generated from protopanaxadiol-type ginsenosides via intestinal microbiota-mediated biotransformation, exhibits anti-inflammatory and vasoprotective properties (Jiao and Jia, 2022; Wang X. et al., 2022). In the context of PAH, ginsenoside Compound K has been shown to effectively inhibit PDGF-BB-induced aberrant proliferation of PASMCs, promote their apoptosis, and reverse pathological phenotypic switching. Through these combined actions, it intervenes at multiple mechanistic levels in the process of pulmonary vascular remodeling (Liu et al., 2021).

3.2.4.4 Pachymic acid

Pachymic acid, a lanostane-type triterpenoid and secondary metabolite isolated from the medicinal fungus Wolfiporia cocos (F.A. Wolf) Ryvarden and Gilb. (syn. Poria cocos; Fam. Polyporaceae), possesses notable anti-oxidative stress and anti-proliferative effects on vascular smooth muscle cells (Zhu et al., 2021; He et al., 2022). In experimental models of PAH, pachymic acid has been shown to activate the Nrf2/Kelch-like ECH-associated protein 1 (Keap1)/antioxidant response element (ARE) signaling pathway, thereby mitigating oxidative damage, suppressing pathological cell proliferation, and ultimately ameliorating PAH-associated pulmonary vascular remodeling (He et al., 2022).

3.2.4.5 Corosolic acid

Corosolic acid, a naturally occurring pentacyclic triterpenoid isolated from the leaves of Lagerstroemia speciosa (L.) Pers. (Fam. Lythraceae), exhibits potent vasoprotective potential in PAH. Experimental studies have shown that corosolic acid markedly suppresses the aberrant proliferation of PASMCs by inhibiting activation of the STAT3 signaling pathway (Kawade et al., 2023). In addition, it attenuates NF-κB activity, thereby downregulating PDGF receptor-β expression while concurrently inhibiting STAT3 expression and phosphorylation. Through these combined actions, corosolic acid effectively ameliorates PAH and its associated pathological vascular remodeling (Yamamura et al., 2024).

3.2.4.6 Asiaticoside

Asiaticoside, a natural pentacyclic triterpenoid saponin predominantly obtained from the phytomedicine Centella asiatica (L.) Urb. (Fam. Apiaceae), possesses anti-inflammatory and anti-apoptotic properties (Dang et al., 2019; Yao et al., 2023). In the context of PAH, asiaticoside has been shown to activate the phosphatidylinositol 3-kinase (PI3K)/AKT/endothelial nitric oxide synthase (eNOS) signaling pathway, thereby enhancing nitric oxide (NO) production, suppressing endothelial cell apoptosis, and improving endothelial function (Wang et al., 2018a). Moreover, asiaticoside attenuates pulmonary vascular remodeling by inhibiting excessive activation of the TGF-β1/mothers against decapentaplegic homolog 2/3 (Smad2/3) signaling cascade, which in turn reduces the aberrant proliferation and migration of PASMCs while promoting their apoptosis (Wang X.-B. et al., 2015).

3.2.4.7 18β-glycyrrhetinic acid

18β-Glycyrrhetinic acid, a principal bioactive triterpenoid aglycone predominantly isolated from the roots of Glycyrrhiza glabra L. (Fam. Fabaceae), exhibits antioxidant and anti-inflammatory effects, and has been shown to markedly improve pulmonary vascular function (Yang T. et al., 2021; Qing et al., 2022; Shanahati et al., 2025). In experimental models of PAH, 18β-glycyrrhetinic acid attenuates inflammation-mediated lung tissue injury, thereby slowing disease progression (Zhang et al., 2019b). Mechanistic studies indicate that 18β-glycyrrhetinic acid suppresses activation of the protein kinase RNA-like endoplasmic reticulum kinase (PERK)/eukaryotic translation initiation factor 2-alpha (eIF2α)/NF-κB signaling pathway, thereby mitigating endoplasmic reticulum stress (ERS)-induced inflammatory responses and alleviating pulmonary vascular remodeling (Wang J.-L. et al., 2022). Additionally, it modulates Ras homolog family member A (RhoA)/Rho-associated coiled-coil containing protein kinase (ROCK) signaling activity, which inhibits abnormal proliferation of human PASMCs (Zhang et al., 2019a).

3.2.4.8 Ursolic acid

Ursolic acid, a naturally occurring pentacyclic triterpenoid widely distributed in plants such as Malus domestica Borkh. (apple), Crataegus spp. (hawthorn), and Origanum vulgare L. (oregano), possesses anti-inflammatory and anti-oxidative stress properties (Erdmann et al., 2021; Zhao et al., 2023). In animal models, ursolic acid has been shown to activate the peroxisome proliferator-activated receptor-α (PPARα)-dependent fatty acid oxidation pathway, thereby ameliorating RV energy metabolic disorders and subsequently suppressing the development and progression of myocardial hypertrophy, fibrosis, apoptosis, and functional impairment (Gao et al., 2020).

3.2.4.9 Astragaloside IV

Astragaloside IV (ASIV), a principal cycloartane-type triterpene saponin isolated from the root of Astragalus membranaceus (Fisch.) Bunge (Fam. Fabaceae), has long been employed in traditional Chinese medicine for the prevention and treatment of cardiovascular diseases (Yang et al., 2023). It exhibits pronounced anti-inflammatory, anti-oxidative, and cardioprotective activities (Zhang D.-Q. et al., 2018). In experimental models of PAH, ASIV significantly lowers PAP, attenuates RVH, and alleviates pulmonary vascular remodeling, thereby preserving lung structural integrity and functional stability (Zhang X. et al., 2018; XinTian et al., 2022). Mechanistic studies have revealed that ASIV mitigates disease progression by downregulating TGF-β and IL-6 levels, consequently suppressing pro-inflammatory signaling cascades (Jin et al., 2021; Niu et al., 2025). Moreover, ASIV enhances endothelial function via upregulation of silent information regulator 1 (SIRT1), which reduces oxidative stress and limits endothelial injury (Leng et al., 2018; Zhang et al., 2021; Niu et al., 2025). It also modulates the Notch signaling pathway-closely implicated in PASMCs proliferation and apoptosis-whereby its inhibition under hypoxic conditions markedly attenuates pulmonary vascular remodeling (Yao et al., 2021). At the vascular protection level, ASIV improves endothelium-dependent vasodilation through SIRT1 upregulation and histone deacetylase (HDAC) inhibition, leading to enhanced eNOS expression and ultimately amelioration of PAH (Leng et al., 2018; Zhang et al., 2021).

3.2.4.10 Celastrol

Celastrol, a bioactive pentacyclic triterpenoid isolated from the phytomedicine Tripterygium wilfordii Hook. f. (Fam. Celastraceae), possesses a broad spectrum of pharmacological activities, with anti-inflammatory and anti-oxidative effects being particularly prominent (Li Z. et al., 2022; Tan et al., 2025). In experimental models of PAH, celastrol markedly reduces PAP and mitigates medial hypertrophy as well as interstitial thickening of small pulmonary arteries (Li et al., 2022a). At the cellular level, under hypoxic conditions, celastrol directly suppresses the proliferation of human PASMCs by downregulating the pro-proliferative basigin (Bsg)/cyclophilin A (CyPA) signaling axis, decreasing intracellular ROS production, and reprogramming mitochondrial energy metabolism, thereby collectively inhibiting abnormal PASMCs growth (Kurosawa et al., 2019; 2021). Furthermore, in lung tissues, celastrol significantly attenuates inflammatory responses by inhibiting NF-κB signaling, contributing to its protective effects against pulmonary vascular remodeling (Li et al., 2022a).

4 Molecular mechanisms underlying the therapeutic effects of terpenoids on PAH

As illustrated in Figure 3, natural terpenoids exert multifaceted, multi-target effects on modulating the development and progression of PAH. Their underlying mechanisms encompass the attenuation of oxidative stress, suppression of inflammatory responses, inhibition of EndMT, regulation of cellular proliferation and apoptosis, and modulation of ion channel activity.

Figure 3

Figure 3. Regulation of PAH by natural terpenoids, including oxidative stress, inflammation, EndMT, proliferation and apoptosis, and ion channel activity.

4.1 Attenuation of oxidative stress

PAH can stimulate the excessive production of ROS in PASMCs, triggering oxidative stress and disrupting the normal function of multiple cellular signaling pathways. Oxidative stress may serve either as the initiating factor or as a downstream consequence of in various pathological processes, including hypoxia, inflammatory responses, and DNA damage, which in turn lead to an imbalance between PASMCs proliferation and apoptosis, pulmonary vascular remodeling and luminal narrowing, as well as abnormal alterations in vascular structure—ultimately contributing to the onset and progression of PAH (Liu H. et al., 2023; Tang et al., 2025). Therefore, suppression of oxidative stress and elimination of excessive ROS are considered effective strategies for the prevention and treatment of PAH.

4.1.1 Direct modulation of oxidative stress factors

The accumulation of ROS is intimately linked to the disruption of redox homeostasis and mitochondrial function. During the onset and progression of PAH, excessive ROS generation drives oxidative stress, pulmonary vascular remodeling, and abnormal proliferation of PASMCs. Natural terpenoids confer protective effects by scavenging ROS, alleviating oxidative stress, and promoting PASMCs apoptosis, thereby attenuating pulmonary vascular remodeling and reducing elevated PAP. In high-altitude-induced PAH animal models, tanshinone IIA has demonstrated a pronounced protective effect against hypoxia. In mice exposed to acute hypobaric hypoxia at an altitude of approximately 4,260 m, tanshinone IIA treatment markedly prolonged survival time by increasing the activities of SOD and LDH and reducing MDA levels in both brain and cardiac tissues after hypoxia exposure (Wang et al., 2020b). In an in vitro PASMCs model exposed to 24 h of hypoxia (3% O₂), carvacrol markedly decreased MDA levels and restored hypoxia-depleted SOD activity and reduced glutathione (GSH) content, thus attenuating oxidative stress (Zhang et al., 2016).

4.1.2 Attenuation of aberrant pulmonary vasoconstriction

Oxidative stress can precipitate endothelial dysfunction and disrupt the finely tuned balance between vasoconstrictors and vasodilators in the pulmonary vasculature. Mechanistically, excessive oxidative stress inhibits eNOS activity and reduces NO bioavailability, thereby impairing endothelium-dependent vasodilation, inducing abnormal pulmonary vasoconstriction, and facilitating vascular remodeling. Consequently, restoration of vasodilatory capacity through antioxidant interventions represents a rational strategy to re-establish normal pulmonary vascular tone and attenuate PAH (Bao et al., 2023; Yu et al., 2025).

Experimental studies have demonstrated that tanshinone IIA can prevent the development of PAH in rats exposed to hypobaric hypoxia at an altitude of approximately 7,620 m (25,000 ft). Pretreatment with tanshinone IIA prior to each hypoxic exposure effectively inhibited hypoxia-induced ROS accumulation and lipid peroxidation in lung tissue, while increasing the GSH/oxidized glutathione (GSSG) ratio, SOD activity, and the expression of Nrf2, heme oxygenase-1 (HO-1), and metallothionein (MT). These changes enhanced the endogenous antioxidant defense capacity of hypoxic lung tissue and reduced oxidative injury. Given that NO and endothelin-1 (ET-1) are major vasoactive mediators governing vasodilation and vasoconstriction, respectively, tanshinone IIA pretreatment not only significantly increased the levels of NO, inducible nitric oxide synthase (iNOS), Na⁺/K⁺-ATPase, and vascular endothelial growth factor (VEGF), but also decreased ET-1 expression. This dual modulation reduced pulmonary vascular contractility and permeability, suppressed pathological vasospasm, and ameliorated vascular abnormalities. Collectively, by reinforcing the antioxidant defense system, rebalancing the NO/ET-1 axis, and improving vasomotor function, tanshinone IIA pretreatment effectively protected against hypoxia-induced pulmonary vascular injury and mitigated PAH progression (Yadav et al., 2025).

4.1.3 Suppression of positive feedback loops associated with inflammation

During the development and progression of PAH, oxidative stress induces the excessive accumulation of reactive oxygen species (ROS). This accumulation directly activates inflammatory-related signaling pathways, and promotes the release of pro-inflammatory cytokines including IL-1β. Furthermore, it upregulates the expression of inflammation-mediated oxidases, which in turn increases ROS production, thus forming a vicious “oxidative stress - inflammation” positive feedback loop. Elevated ROS levels can promote phenotypic transformation and abnormal proliferation of PASMCs, directly leading to pulmonary vascular remodeling (Liu H. et al., 2023). The inflammatory environment can trigger endothelial dysfunction and vascular inflammation, thereby creating a self-perpetuating positive feedback loop between oxidative stress and inflammation. Over time, this vicious cycle accelerates pulmonary artery remodeling and leads to the occurrence and development of PAH (Poyatos et al., 2023).

In a MCT-induced PAH rat model, crocin markedly inhibited inflammatory signaling mediated by the chemokine CCL2 and its receptor CCR2. Treatment with crocin significantly downregulated both mRNA and protein expression of TNF-α, IL-6, IL-1β, and iNOS in lung tissue. Furthermore, oxidative stress biomarkers in PAH rat lungs showed marked dysregulation, with increased MDA levels and decreased activities of SOD and GSH-PX. Crocin intervention effectively reversed these alterations, thereby mitigating oxidative injury. Regarding RV remodeling, PAH model rats exhibited substantially elevated mRNA and protein levels of TNF-α, IL-6, and IL-1β in RV tissue, accompanied by cardiomyocyte hypertrophy, thickened myocardial fibers, interstitial inflammatory cell infiltration, and edema. Crocin treatment reduced the expression of these inflammatory mediators, restored normal myocardial architecture, and alleviated cardiac hypertrophy and inflammation-associated injury. Consequently, crocin ameliorated pulmonary vascular remodeling and partially prevented PAH progression. Collectively, these findings suggest that crocin exerts protective effects in PAH by simultaneously suppressing oxidative stress and inflammatory responses, thereby improving pathological alterations in both the pulmonary vasculature and cardiac tissue (Sheng et al., 2022).

In the same model, paclitaxel treatment also effectively reversed the reduction in endogenous antioxidant enzyme activities (such as SOD, GSH-Px, and CAT) and total antioxidant capacity (TAC), as well as the increase in malondialdehyde (MDA) levels. At the same time, it reduced the expression of pro-inflammatory cytokines TNF-α and IL-6 in lung tissue. Paclitaxel restored antioxidant enzyme activities and total antioxidant capacity and inhibited the production of pro-inflammatory cytokines. These molecular and biochemical improvements translated into better hemodynamic function, including reduced right ventricular systolic pressure and decreased pulmonary artery wall thickness, ultimately alleviating the severity of PAH (Beik et al., 2021). Further studies have shown that paclitaxel also downregulated the expression of microRNA-204 (miR-204) in the right ventricle of PAH rats, increased the antioxidant/oxidant ratio, and improved ventricular function, thereby exerting significant cardioprotective effects (Rajabi et al., 2021).

4.1.4 Activation of the OXR1 signaling pathway

Oxidation resistance 1 (OXR1) is a critical regulatory factor in the cellular oxidative stress response. It mitigates oxidative damage primarily by upregulating the transcription of genes encoding antioxidant enzymes, thereby indirectly scavenging excessive ROS (Xu et al., 2023). Experimental evidence indicates that crocin can activate the OXR1 signaling pathway in PAH. In MCT-induced PAH rats, pulmonary tissue exhibited significantly reduced expression of OXR1 and its downstream target genes p21 and Nrf2 compared with control animals. Crocin intervention markedly reversed these changes, concomitantly activating the p21/Nrf2 antioxidant pathway. As a result, crocin restored the activities of GSH-Px, SOD, CAT, and GSH, while reducing MDA levels, thereby substantially enhancing overall antioxidant capacity. Beyond its antioxidative effects, crocin reduced collagen deposition in pulmonary tissue, decreased pulmonary arterial wall thickness, suppressed inflammatory cell infiltration, and improved histopathological architecture in the lungs of MCT-induced PAH rats. Collectively, these actions effectively inhibited the onset and progression of PAH. In summary, crocin exerts protective effects on the pulmonary vasculature and lung tissue by activating the OXR1/p21/Nrf2 antioxidant signaling axis, thereby synergistically attenuating oxidative stress and inflammatory responses (Xu et al., 2023).

4.1.5 Regulation of the Nrf2/Keap1/ARE signaling pathway

Nrf2 is a stress-responsive transcription factor that plays a pivotal role in coordinating the cellular defense mechanisms against oxidative stress-induced injury. By regulating the transcription of a wide array of antioxidant and cytoprotective genes, Nrf2 helps maintain redox homeostasis and intracellular equilibrium (Hasan et al., 2025). Under basal conditions, Keap1 binds Nrf2 in the cytoplasm and promotes its ubiquitination and proteasomal degradation, thereby keeping intracellular Nrf2 levels low. Upon oxidative stress, conformational modification of Keap1 leads to its dissociation from Nrf2, allowing Nrf2 to translocate into the nucleus, bind to ARE in target gene promoters, and initiate transcription of downstream antioxidant genes (Tossetta et al., 2023). As shown in the Nrf2 part in Figure 4.

Figure 4

Figure 4. Molecular mechanisms of natural terpenoids in the treatment of PAH: inhibition of oxidative stress, suppression of inflammation, blockade of EndMT, regulation of cell proliferation and apoptosis, and regulation of Ion Channels.

Preclinical studies have demonstrated that pachymic acid can alleviate hypoxia-induced PAH in rats via activation of the Nrf2/Keap1/ARE signaling pathway, thereby reversing RVH and pulmonary vascular remodeling (He et al., 2022). In vivo, administration of pachymic acid significantly decreased MDA levels in lung tissue, while upregulating the expression and activity of GSH-Px and SOD. In vitro experiments using hypoxia-exposed PASMCs further confirmed that hypoxic stress downregulated Nrf2 expression and upregulated Keap1 expression, whereas pachymic acid treatment effectively reversed these molecular alterations. Notably, co-administration of an Nrf2 inhibitor abolished the protective effects of pachymic acid, indicating that its anti-PAH efficacy is critically dependent on Nrf2/Keap1/ARE pathway activation. In summary, pachymic acid confers significant protection against hypoxia-induced PAH by modulating the Nrf2/Keap1/ARE axis, enhancing antioxidant defenses, and mitigating pulmonary vascular and cardiac remodeling.

4.2 Inhibition of inflammatory responses

Inflammation constitutes a pivotal pathological mechanism underlying the initiation and progression of PAH. In lung tissues from PAH rat models, pronounced neutrophil infiltration has been documented (Fadón-Padilla et al., 2024). The ensuing inflammatory microenvironment precipitates a cascade of pathological alterations in the pulmonary vasculature, including endothelial dysfunction, aberrant proliferation of PASMCs, and adventitial fibrosis. Collectively, these changes contribute to pulmonary vascular remodeling and an increase in PVR. Terpenoids exhibit significant cardiopulmonary protective potential by attenuating inflammatory responses and mitigating inflammation-mediated vascular pathology. Through suppression of pro-inflammatory signaling and downstream effector molecules, these compounds can effectively delay or prevent the structural and functional deterioration characteristic of PAH, thereby curbing disease development and progression.

4.2.1 Regulation of pro-inflammatory cytokine release

Inflammatory processes can stimulate the release of a wide spectrum of pro-inflammatory cytokines. In patients with PAH, elevated levels of cytokines, inflammatory mediators, and immune cell infiltration are frequently observed around the pulmonary vasculature. Acting through multiple interconnected signaling pathways, these factors synergistically regulate pulmonary vascular remodeling and fuel the progression of PAH (Hu et al., 2020).

In a MCT-induced PAH rat model, D-limonene markedly attenuated cardiac inflammation and fibrosis, leading to improved cardiac function. PAH model rats exhibited significantly elevated mRNA expression of IL-1β, IL-6, and TNF-α in the right ventricle, alongside decreased levels of the anti-inflammatory cytokines IL-10 and TGF-β. Treatment with D-limonene restored these parameters to near-control levels, suggesting that its cardioprotective effects are primarily mediated by suppression of pro-inflammatory cytokine release, thereby alleviating myocardial inflammation and fibrosis and mitigating PAH severity (Teixeira-Fonseca et al., 2024).

Similarly, in MCT-induced PAH models, perillyl alcohol treatment effectively reduced RVSP and RVH index, normalized pulmonary artery wall thickness, and markedly improved pulmonary hemodynamics. Histopathological examination revealed severe pulmonary inflammatory responses in untreated PAH rats, characterized by elevated IL-1β and interleukin-8 (IL-8) levels, whereas perillyl alcohol administration significantly suppressed these inflammatory markers. These findings underscore the role of perillyl alcohol in suppressing pulmonary vascular inflammation, attenuating vascular remodeling, and alleviating PAH pathophysiology (Rajabi et al., 2020).

4.2.2 Inhibition of the NF-κB signaling pathway

NF-κB is a key transcription factor regulating inflammatory responses. It can be activated via upstream Toll-like receptors (TLRs) or ROS signaling, and participates in the pathogenesis of various pulmonary diseases (Cui et al., 2025). In the pulmonary arterial intima of patients with chronic thromboembolic pulmonary hypertension, positive expression of phosphorylated NF-κB-p65 has been detected, indicating that the lungs are in an inflammatory state, with part of the process mediated by the NF-κB signaling pathway (Smolders et al., 2021). Activation of NF-κB promotes the expression of various pro-inflammatory mediators, such as IL-6 and chemokine CXCL10, both of which are significantly upregulated in PAH patients and experimental models (Wang R.-R. et al., 2022).

In a MCT-induced PAH rat model, prophylactic administration of paeoniflorin markedly reduced inflammatory cell infiltration in lung tissue, decreased the number of macrophages/monocytes and mast cells around pulmonary arteries, and downregulated mRNA expression of IL-6, IL-1β, and TNF-α. Furthermore, in PDGF-BB-induced PASMCs, paeoniflorin dose-dependently inhibited phosphorylation of the NF-κB p65 subunit, indicating that its anti-inflammatory effect is mediated, at least in part, through suppression of the NF-κB pathway, thereby preventing and treating PAH (Yu M. et al., 2022).

In addition, in a PDGF-BB-induced human PASMCs model, 18β-glycyrrhetinic acid inhibited endoplasmic reticulum stress activation, reduced phosphorylated NF-κB p65 expression, and upregulated IκB protein levels, thereby preventing NF-κB nuclear translocation. Animal experiments demonstrated that this compound significantly improved hemodynamic and histopathological parameters, reduced the RVH index, and alleviated pulmonary vascular remodeling. These findings suggest that the therapeutic effect of 18β-glycyrrhetinic acid on PAH is likely mediated through inhibition of the NF-κB signaling pathway (Wang J.-L. et al., 2022). As shown in the NF-κB part of Figure 4.

4.3 Inhibition of EndMT

EndMT is a pathological process in which PAECs lose their characteristic endothelial phenotype and functions, concomitantly acquiring mesenchymal-like properties such as enhanced migratory and invasive capacities. This phenotypic shift is marked by downregulation of endothelial markers [e.g., vascular endothelial cadherin, cluster of differentiation 31 (CD31)] and upregulation of mesenchymal markers (e.g., α-SMA, vimentin). EndMT plays a pivotal role in pulmonary arterial remodeling, contributing to medial and adventitial thickening, luminal narrowing, and a sustained increase in PAP. Over time, these structural and hemodynamic alterations drive both the onset and progression of PAH (Jiao et al., 2025).

4.3.1 Activation of the BMP pathway

Loss-of-function mutations in the BMPR2 gene are among the leading genetic causes of both familial and idiopathic PAH. Such mutations attenuate canonical bone morphogenetic protein (BMP) signaling while relatively enhancing TGF-β signaling, disrupting the homeostatic balance between these two pathways. This imbalance facilitates EndMT, promotes vascular remodeling and luminal narrowing of pulmonary arteries, and ultimately contributes to PAH onset and progression (Sharmin et al., 2021; Wang C. et al., 2022).

In a SU5416/hypoxia (SuHx)-induced PAH rat model, prophylactic administration of paeoniflorin markedly attenuated RVH and fibrosis. Lung tissue from SuHx-exposed rats displayed significant downregulation of the endothelial marker vascular endothelial cadherin (VE-cadherin) and concomitant upregulation of mesenchymal markers, including fibronectin and vimentin—hallmarks of EndMT. Paeoniflorin treatment restored VE-cadherin expression and reduced fibronectin and vimentin levels, suggesting that it suppresses EndMT in vivo. Consistent results were observed in an in vitro hypoxia-induced human PAECs model, where hypoxia triggered EndMT in a time-dependent manner. This was characterized by marked upregulation of α-SMA, fibronectin, vimentin, and EndMT-associated transcription factors Snail and Twist, alongside reduced VE-cadherin expression. Paeoniflorin reversed the hypoxia-induced downregulation of VE-cadherin and partially attenuated the upregulation of vimentin and fibronectin, thereby mitigating EndMT progression. Mechanistic investigations revealed that hypoxia significantly decreased BMPR2 expression and phosphorylation of its downstream effectors SMAD1/5 in human PAECs, whereas paeoniflorin effectively restored both BMPR2 protein levels and SMAD1/5 phosphorylation. Importantly, siRNA-mediated BMPR2 knockdown markedly blunted paeoniflorin’s inhibitory effect on hypoxia-induced EndMT, indicating that its anti-EndMT activity is dependent on BMPR2 upregulation. In summary, paeoniflorin suppresses hypoxia- and SuHx-induced EndMT by restoring BMPR2 expression and activating the BMPR2–SMAD1/5 signaling axis, thereby attenuating pulmonary vascular remodeling and contributing to the prevention and treatment of PAH (Yu et al., 2020).

4.3.2 Inhibition of the AKT/GSK-3β signaling pathway

The AKT signaling pathway can phosphorylate and inhibit glycogen synthase kinase-3β (GSK-3β), thereby preventing the proteasomal degradation of β-catenin. Aberrant accumulation of β-catenin is a critical driver of EndMT and can potentiate pulmonary vascular remodeling (Wu et al., 2023).

In a MCT-induced PAH rat model, curcumol exhibited dose-dependent protective effects, significantly reducing RVH and pulmonary arterial wall thickening. Lung tissues from MCT-treated rats displayed markedly elevated protein levels of phosphorylated AKT (p-AKT) and phosphorylated GSK-3β (p-GSK-3β), indicating activation of the AKT/GSK-3β cascade. Curcumol administration notably suppressed this phosphorylation, concomitant with downregulation of overexpressed mesenchymal markers—vimentin and α-SMA—as well as the EndMT-associated transcription factor Snail, thereby reversing MCT-induced EndMT in vivo. Consistent findings were observed in vitro. Rat PAECs exposed to EndMT-inducing medium exhibited a significant increase in the proportion of α-SMA-positive cells, decreased protein expression of endothelial markers CD31 and von Willebrand factor (vWF), and elevated vimentin, α-SMA, and Snail expression. Curcumol treatment reversed these alterations, restoring CD31 and vWF levels while reducing mesenchymal marker and transcription factor abundance. Moreover, curcumol inhibited p-AKT and p-GSK-3β expression in PAECs. Notably, co-administration of curcumol with the PI3K inhibitor LY294002 resulted in lower vWF protein expression than LY294002 treatment alone, indicating that curcumol’s modulation of EndMT is mechanistically linked to suppression of the AKT/GSK-3β axis rather than redundant with PI3K inhibition. In summary, curcumol attenuates the initiation and progression of EndMT by inhibiting the AKT/GSK-3β/β-catenin signaling pathway, thereby reducing vascular remodeling and improving cardiopulmonary function in PAH (Nie et al., 2023). As shown in the AKT part of Figure 4.

4.4 Regulation of proliferation and apoptosis

Abnormal proliferation of PASMCs is a central pathological feature of PAH, driving progressive pulmonary vascular wall remodeling and luminal narrowing. In this context, PASMCs frequently acquire apoptosis resistance, thereby enhancing their survival and propensity for accumulation (Vitry et al., 2021). In parallel, excessive apoptosis of vascular endothelial cells (ECs)—coupled with dysfunction of residual ECs—constitutes another critical factor in vascular remodeling, further accelerating the initiation and progression of PAH (Humbert et al., 2004; Zhang Q. et al., 2024). This dual cellular imbalance—hyperproliferation of PASMCs combined with excessive apoptosis of ECs—represents a defining hallmark of vascular pathology in PAH, leading to sustained structural and functional compromise of the pulmonary vasculature. Consequently, therapeutic strategies that simultaneously suppress aberrant PASMCs proliferation and protect ECs from apoptosis are of particular significance. Natural terpenoids are increasingly recognized for exerting anti-PAH effects, at least in part, through restoring the proliferation–apoptosis equilibrium within the pulmonary vascular wall.

4.4.1 Regulation of the PI3K/AKT pathway

Activation of the PI3K/AKT signaling pathway can inhibit autophagy and apoptosis in vascular ECs, promoting a shift toward an anti-apoptotic phenotype (Tang Q. et al., 2023). In a hypoxia-induced PAH rat model, asiaticoside effectively suppressed pulmonary vascular remodeling and alleviated endothelial injury, accompanied by a marked upregulation of p-AKT/AKT and p-eNOS/eNOS in lung tissues. Similarly, in in vitro hypoxia-stimulated human PAECs, terminal deoxynucleotidyl transferase dUTP nick-end labeling assay and caspase-3 activity measurements showed that hypoxia significantly increased endothelial apoptosis, whereas asiaticoside treatment substantially reversed this effect, reducing both apoptotic cell proportion and caspase-3 enzymatic activity. Mechanistic analyses demonstrated that asiaticoside markedly enhanced the phosphorylation levels of AKT and eNOS under hypoxic conditions. Importantly, this effect was abolished by co-treatment with the PI3K inhibitor LY294002, indicating that asiaticoside’s anti-apoptotic and vasculoprotective activity is dependent on activation of the PI3K/AKT signaling cascade. In summary, asiaticoside mitigates apoptosis of human PAECs by activating the PI3K/AKT/eNOS pathway, thereby reducing endothelial injury, alleviating pulmonary vascular remodeling, and improving the pathological profile of hypoxia-induced PAH (Wang et al., 2018a). As shown in the PI3K part of Figure 4.

4.4.2 Inhibition of the MAPK pathway

The MAPK signaling pathway is one of the central molecular mechanisms driving the onset and progression of PAH, comprising major subfamilies such as ERK1/2, c-Jun N-terminal kinase, and p38 MAPK. Hypoxia, inflammatory cytokines, and diverse growth factors can activate the MAPK cascade, leading to induction of downstream transcription factors and cell cycle regulators (e.g., Cyclins). This activation promotes the phenotypic switch of PASMCs from a quiescent, contractile phenotype to a synthetic state, characterized by abnormal proliferation, increased migratory capacity, and resistance to apoptosis—ultimately accelerating pulmonary vascular remodeling (Vanderpool et al., 2017).

In hypoxia-induced PASMCs, ASIV decreased the proportion of proliferating cell nuclear antigen (PCNA)-positive cells, downregulated hypoxia-induced expression of hypoxia-inducible factor-1α (HIF-1α) and phosphorylated ERK1/2, while upregulating cell cycle inhibitors p27 and p21 as well as pro-apoptotic proteins Bax, caspase-9, and caspase-3 (Jin et al., 2021).

It is noteworthy that the regulatory effects of ASIV on ERK1/2 phosphorylation appear to be context-dependent, varying with disease model and cell type. For instance, in certain endothelial injury models, ASIV has been reported to activate ERK1/2, thereby promoting endothelial repair rather than inhibition (Liu Y. et al., 2023). As shown in the MAPK/ERK part of Figure 4.

4.4.3 Inhibition of the Notch pathway

In patients with PAH, the Notch ligand Jagged-1 is markedly overexpressed in PASMCs and drives their sustained proliferation through selective activation of Notch3 signaling in an autocrine manner. This aberrant activation not only elevates PVR and facilitates PAH onset, but also induces oxidative stress and endoplasmic reticulum stress, while inhibiting vascular cell apoptosis (Zhang Y. et al., 2022).

Evidence further indicates that in PASMCs derived from PAH patients, Notch3 mutations can enhance ROS production and suppress NO synthesis, thereby reducing apoptosis and maintaining a contractile phenotype (Morris et al., 2023). In a hypoxia-induced PAH rat model, PCNA levels were significantly elevated and the walls of small pulmonary arteries were notably thickened. ASIV treatment markedly alleviated these pathological changes, reducing pulmonary vascular remodeling. In vitro, hypoxia significantly promoted PASMCs proliferation and increased the proportion of cells in S and G₂/M phases of the cell cycle, whereas ASIV inhibited excessive proliferation and decreased the percentage of cells in these proliferative phases. Mechanistic investigations revealed that ASIV suppressed the expression of Jagged-1, Notch-3, and the downstream transcription factor Hairy and Enhancer of Split-5. In summary, ASIV appears to ameliorate pulmonary vascular remodeling and slow or reverse PAH progression by inhibiting the Notch/Jagged-1 signaling pathway, thereby blocking aberrant PASMCs proliferation and cell cycle progression (Yao et al., 2021). As shown in the Jagged-1 part of Figure 4.

4.5 Regulation of ion channels

Dysfunction of potassium (K⁺) ion channels represents one of the core pathological features of PAH, whereas aberrant activation of Ca²⁺ ion channels serves as a major driving force for pulmonary vascular remodeling. Alterations in ion channel function—whether due to abnormal membrane potential regulation, disruption of intracellular Ca²⁺ homeostasis, or pathological mutations in channel-encoding genes—collectively contribute to sustained pulmonary vasoconstriction, progressive structural remodeling of the pulmonary vasculature, and eventual right ventricular failure (Masson et al., 2022; Villegas-Esguevillas et al., 2023).

4.5.1 Enhancing voltage-dependent potassium channel activity

Voltage-dependent potassium (Kv) channels are among the principal determinants of resting membrane potential in PASMCs (Mondéjar-Parreño et al., 2021). Downregulation of Kv channel expression or attenuation of Kv currents leads to membrane depolarization of PASMCs, which in turn reduces apoptosis, promotes excessive proliferation, and ultimately drives pulmonary vascular remodeling. Under acute hypoxic conditions, tanshinone IIA has been shown to reverse the hypoxia-induced suppression of Kv currents in PASMCs. In rat models of PAH induced by chronic intermittent or sustained hypoxia, tanshinone IIA treatment significantly lowered RVSP, reduced the RVH index, and attenuated pulmonary vascular remodeling. Furthermore, tanshinone IIA markedly upregulated both mRNA and protein expression of Kv1.5 and Kv2.1 channels in small pulmonary arteries, thereby restoring Kv currents in PASMCs. These findings suggest that tanshinone IIA may alleviate sustained pulmonary vasoconstriction and vascular structural remodeling by directly enhancing Kv channel expression and function, thus preventing membrane depolarization—an effect that may represent a key mechanism underlying its therapeutic efficacy in hypoxia-induced PAH (Zheng et al., 2015). As shown in the Kv part of Figure 4.

4.5.2 Regulating intracellular Ca²⁺ concentration to inhibit vascular remodeling

Sustained elevation of intracellular Ca²⁺ concentration in PASMCs is a key driver of abnormal cell proliferation and migration, leading to vascular wall thickening and occlusive remodeling, and thus plays a central role in the pathogenesis of PAH (Masson et al., 2022; Zhang et al., 2024a). Modulation of voltage-dependent Ca²⁺ channel activity can directly influence intracellular Ca²⁺ homeostasis, thereby regulating pulmonary artery tone and overall hemodynamics (Jain et al., 2021).

In rat models of PAH induced by chronic hypoxia or MCT, ginsenoside Rb1 significantly inhibited pulmonary artery contraction induced by ET-1 and cyclopiazonic acid, and reduced both cyclopiazonic acid-activated Ca²⁺ influx and non-selective cation entry in PASMCs. Treatment with ginsenoside Rb1 markedly decreased the amplitude of cyclopiazonic acid-induced Ca²⁺ transients and the Mn²⁺ quenching rate, while restoring the elevated resting intracellular Ca²⁺ levels observed in PAH models. Importantly, the selective SOCE pathway inhibitor gadolinium completely abolished the vasodilatory effect of ginsenoside Rb1, indicating that its action is mediated through specific inhibition of the SOCE pathway. By lowering intracellular Ca²⁺ concentrations in PASMCs, ginsenoside Rb1 counteracts the augmented pulmonary vasoconstriction and hyperreactivity characteristic of PAH, thereby offering a potential therapeutic strategy grounded in Ca²⁺ signal modulation (Wang R.-X. et al., 2015). As shown in the Ca²⁺ part of Figure 4.

5 Safety considerations and therapeutic limitations

Although terpenoids demonstrate promising potential, their translation from basic research to clinical application is severely constrained by their toxicological profiles. The safety of these compounds varies significantly. They range from well-tolerated food additives to agents with narrow therapeutic indices that necessitate structural modification or targeted delivery systems.

5.1 Well-tolerated agents and dose-dependent effects

Many monoterpenes and specific terpenoids exhibit favorable safety profiles. This is supported by their historical use in traditional medicine and their status as food additives. Specifically, D-Limonene, 1,8-Cineole, and Carvacrol hold “Generally Recognized as Safe” status (Chen et al., 2016; Salehi et al., 2019). D-Limonene shows low toxicity. Nephropathy has been observed only in male rats, via a mechanism irrelevant to humans. However, high doses may cause gastrointestinal irritation (Kim et al., 2013). Similarly, 1,8-Cineole and Carvacrol are generally safe. Nevertheless, they may cause mucosal irritation. In cases of extreme overdose, they can lead to neurotoxicity (Khosravi and Erle, 2016; Dosoky and Setzer, 2018). Likewise, Crocin and Astragaloside IV show no significant cytotoxicity in major organs at effective pharmacological doses. They demonstrate high safety margins. This makes them ideal candidates for long-term PAH management (Ren et al., 2013; Alavizadeh and Hosseinzadeh, 2014). However, safety is not absolute. Perillyl alcohol is a structural analog of limonene. Yet, it exhibited dose-limiting gastrointestinal toxicity (nausea and vomiting) in clinical trials. This suggests that inhalation administration may be necessary for PAH treatment to bypass gastrointestinal adverse effects (DA Fonseca et al., 2013).

5.2 Compounds with narrow therapeutic windows

For certain diterpenoids and triterpenoids, the narrow margin between therapeutic efficacy and organ toxicity presents a major obstacle. Triptolide has a narrow therapeutic window. It exhibits multi-organ toxicity, particularly hepatotoxicity, nephrotoxicity, and severe reproductive toxicity (such as amenorrhea and inhibition of spermatogenesis). These issues strictly limit its systemic application (Xi et al., 2017). Celastrol is effective in remodeling pulmonary vasculature. However, it carries risks of cardiotoxicity and infertility. Furthermore, its poor water solubility often necessitates administration via toxic vehicles (Kannaiyan et al., 2011). Fumagillin is potent in inhibiting angiogenesis. Yet, its clinical development has historically been hindered by severe neurotoxicity and thrombocytopenia at therapeutic doses (Wei J. et al., 2022). Oridonin shows rapid plasma clearance in animal models. Additionally, it exhibits potential gastrointestinal toxicity (Yang Y.-S. et al., 2021).

5.3 Specific adverse effects relevant to PAH pathophysiology

Certain compounds may exhibit side effects that exacerbate cardiovascular instability in PAH patients. Long-term administration of 18β-Glycyrrhetinic acid induces pseudoaldosteronism. This results in sodium retention, hypokalemia, and hypertension (Isbrucker and Burdock, 2006). Fluid retention and systemic hypertension are particularly detrimental to PAH patients with compromised right ventricular function. Therefore, strict monitoring is required. Alternatively, the drug should be contraindicated in salt-sensitive individuals. Andrographolide typically exhibits hepatoprotective effects. However, cumulative high doses may lead to renal injury (Li X. et al., 2022).

5.4 Pharmacokinetic interactions

Tanshinone IIA, Ginsenoside Rb1, Ginsenoside Rg1, and Curcumol modulate CYP450 enzymes and P-glycoprotein (Qiu et al., 2014; Gao et al., 2021; Chen et al., 2022). Specifically, Tanshinone IIA may enhance or inhibit warfarin metabolism. This alteration increases the risk of bleeding. For PAH patients receiving anticoagulant therapy, this represents a critical safety consideration (Chen et al., 2019). Asiaticoside also displays varying degrees of CYP450 inhibitory potential. Therefore, rigorous interaction studies are essential before conducting clinical combination trials (Pan et al., 2014). In summary, agents like Astragaloside IV and D-Limonene appear ready for human safety testing. Conversely, compounds such as Triptolide, Celastrol, and Fumagillin may require nanoparticle encapsulation or structural modification to widen their therapeutic windows. Furthermore, caution is required in designing clinical trials for PAH. The mineralocorticoid-like effects of 18β-Glycyrrhetinic acid must be carefully managed. Similarly, the drug interaction potential of Ginsenosides and Tanshinone IIA requires strict attention.

6 Conclusions and perspectives

This systematic review identified 23 natural terpenoids encompassing diverse structural subtypes: 5 monoterpenes, 3 sesquiterpenes, 5 diterpenes, and 10 triterpenes. These compounds have been investigated primarily for their potential to modulate PAH-related signaling pathways and suppress aberrant proliferation of PASMCs. Accumulating evidence shows that natural terpenoids act through multiple, overlapping molecular mechanisms, including regulation of oxidative stress, suppression of inflammation, inhibition of EndMT, modulation of cell proliferation and apoptosis, and restoration of ion channel homeostasis. In terms of antioxidant effects, they regulate HIF-1α, OXR1, and Nrf2/Keap1/ARE signaling, lower MDA levels, and restore SOD and GSH activity. These actions enhance ROS clearance, alleviate oxidative stress–mediated PASMCs proliferation and apoptosis, and ultimately slow the progression of PAH (Wang et al., 2020b). To address the excessive PASMCs proliferation that constitutes a core pathological feature of PAH, terpenoids modulate PI3K/AKT, MAPK, and Notch pathways, and regulate Bcl-2 and Bax expression, thereby limiting PASMC growth and reducing apoptosis of human PAECs, which improves the proliferative/anti-apoptotic phenotype (Wang et al., 2018a).Anti-inflammatory effects are mediated through the suppression of IL-6 and CXCL10 via NF-κB signaling. They also involve the inhibition of NF-κB nuclear translocation. In some cases, these compounds downregulate endoplasmic reticulum stress activation. Collectively, these actions reshape the inflammatory microenvironment and slow PAH progression (Wang J.-L. et al., 2022). Regarding EndMT regulation, terpenoids influence the BMP and AKT/GSK3β pathways. This reduces EndMT activity and prevents endothelial phenotypic switching. Consequently, these effects delay vascular remodeling (Nie et al., 2023). Furthermore, these agents modulate ion channel dynamics by activating potassium channels to promote pulmonary vasodilation. They also inhibit calcium channel activation. This decreases Ca²⁺ influx and reduces vascular smooth muscle contractility. Ultimately, these combined mechanisms mitigate vascular remodeling (Wang R.-X. et al., 2015; Zheng et al., 2015). Overall, natural terpenoids display multi-target, multi-pathway, and pleiotropic therapeutic advantages in PAH, highlighting their promise as candidates for further drug development and clinical translation. The underlying mechanisms are summarized in Figure 4.

Natural terpenoids exhibit significant anti-inflammatory, anti-proliferative, and vasodilatory activities in preclinical PAH models. However, their clinical translation faces severe pharmacokinetic challenges. First, extremely low water solubility presents a primary barrier to absorption. Most terpenoids fall under Class II or IV of the Biopharmaceutics Classification System (BCS). Notable examples include Tanshinone IIA, Oridonin, Ursolic acid, Celastrol, Corosolic acid, and Pachymic acid. These compounds dissolve poorly in gastrointestinal fluids. Consequently, their oral bioavailability remains critically low (Rosa et al., 2020; Li M. et al., 2022; Li J. et al., 2022; Wei C. et al., 2022; Sobral et al., 2023; Kadsanit et al., 2024). Second, poor membrane permeability and efflux pump mechanisms further hinder systemic absorption. Macromolecular saponins, such as Astragaloside IV, Ginsenoside Rg1, and Asiaticoside, exhibit high polarity and molecular weight. As a result, they penetrate the intestinal epithelial barrier inefficiently (Han and Fang, 2006; Huang et al., 2006; Zhang and Zhang, 2015). Concurrently, Paeoniflorin and Andrographolide are confirmed substrates of P-glycoprotein. They undergo active efflux by intestinal epithelial cells, which significantly lowers plasma drug concentrations (Liu et al., 2006; Ye et al., 2011). Furthermore, poor metabolic stability and rapid elimination are key bottlenecks in maintaining effective therapeutic concentrations. Volatile monoterpenes (e.g., D-Limonene, Perillyl alcohol) and sesquiterpenes (e.g., Parthenolide, 1,8-Cineole) undergo extensive first-pass metabolism or oxidation in vivo. This results in extremely short half-lives (Cheng et al., 2005; McLean et al., 2007; Sun, 2007; Freund et al., 2020). In contrast, Crocin requires hydrolysis by intestinal flora into crocetin prior to absorption. This conversion process is inefficient and exhibits significant inter-individual variability (Zhang Y. et al., 2019; Shakya et al., 2020). Moreover, potent compounds like Triptolide and Fumagillin are associated with severe hepatorenal or neurotoxicity. Consequently, they possess narrow therapeutic windows (Stockmann-Juvala and Savolainen, 2008; Zhou et al., 2018). Given these multiple pharmacokinetic limitations, developing nanodelivery systems is essential to unlock the therapeutic potential of these natural products. Promising strategies include the use of liposomes, polymeric micelles, or solid lipid nanoparticles. These systems not only significantly improve solubility and bioavailability but also prolong circulation time. Additionally, they enable lung-targeted delivery, thereby enhancing efficacy while reducing systemic toxicity.

Despite promising preclinical prospects, most terpenoids have not entered registered clinical trials for PAH. Current evidence remains limited to in vitro studies and animal models. The primary bottlenecks impeding clinical application stem from unfavorable pharmacokinetic profiles. Specifically, these include extremely low oral bioavailability, non-specific tissue distribution, and narrow therapeutic indices. The dose-limiting toxicity of Triptolide serves as a notable example. To overcome these translational hurdles, future research must prioritize two strategies. The first involves optimizing physicochemical properties and metabolic stability via structural modification. The second entails developing advanced delivery systems, particularly inhalable nanocarriers. These systems enable targeted accumulation within the pulmonary vasculature, thereby reducing systemic toxicity. Simultaneously, a “drug repurposing” strategy should be adopted. Given their established safety profiles, small-scale exploratory clinical trials for PAH are warranted. Such efforts will facilitate the transition of these natural products from bench to bedside.

In conclusion, this review synthesizes the current knowledge regarding natural terpenoids in PAH treatment and underscores their considerable promise. These insights are expected to guide the development of next-generation therapeutic agents that are more effective, safer, and naturally derived, with substantial translational potential for clinical application.

Author contributions

KD: Formal Analysis, Writing – original draft, Conceptualization, Investigation. JZ: Writing – original draft, Writing – review and editing, Formal Analysis, Validation, Project administration. KY: Writing – review and editing. XnL: Writing – review and editing, Conceptualization, Formal Analysis. YZ: Writing – review and editing. XY: Writing – review and editing. XaL: Supervision, Writing – review and editing. CZ: Formal Analysis, Writing – review and editing, Conceptualization, Funding acquisition.

Funding

The author(s) declared that financial support was received for this work and/or its publication. This work was supported by the 2022 “Tianfu Qingcheng Plan” Tianfu Science and Technology Leading Talents Project (Chuan Qingcheng No. 1090), Joint Innovation Fund of Health Commission of Chengdu and Chengdu University of Traditional Chinese Medicine (WXLH202402005, WXLH202403091) and The China Postdoctoral Science Foundation (2024MD763923).

Conflict of interest

The author(s) declared that this work was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The author(s) declared that generative AI was not used in the creation of this manuscript.

Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2025.1713745/full#supplementary-material

References

Abdul Ghani, M. A., Ugusman, A., Latip, J., and Zainalabidin, S. (2023). Role of terpenophenolics in modulating inflammation and apoptosis in cardiovascular diseases: a review. Int. J. Mol. Sci. 24, 5339. doi:10.3390/ijms24065339

PubMed Abstract | CrossRef Full Text | Google Scholar

Alavizadeh, S. H., and Hosseinzadeh, H. (2014). Bioactivity assessment and toxicity of crocin: a comprehensive review. Food Chem. Toxicol. 64, 65–80. doi:10.1016/j.fct.2013.11.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Alves-Silva, J. M., Zuzarte, M., Marques, C., Viana, S., Preguiça, I., Baptista, R., et al. (2022). 1,8-Cineole ameliorates right ventricle dysfunction associated with pulmonary arterial hypertension by restoring connexin43 and mitochondrial homeostasis. Pharmacol. Res. 180, 106151. doi:10.1016/j.phrs.2022.106151

PubMed Abstract | CrossRef Full Text | Google Scholar

Alves-Silva, J. M., Zuzarte, M., Marques, C., Rodrigues, T., Barbeitos, J., Caetano, R., et al. (2025). 1,8-Cineole reduces pulmonary vascular remodelling in pulmonary arterial hypertension by restoring intercellular communication and inhibiting angiogenesis. Phytomedicine 137, 156334. doi:10.1016/j.phymed.2024.156334

PubMed Abstract | CrossRef Full Text | Google Scholar

Anandakumar, P., Kamaraj, S., and Vanitha, M. K. (2021). D-limonene: a multifunctional compound with potent therapeutic effects. J. Food Biochem. 45, e13566. doi:10.1111/jfbc.13566

PubMed Abstract | CrossRef Full Text | Google Scholar

Bao, Y.-R., Chen, J.-W., Jiang, Y., Wang, L.-H., Xue, R., Qian, J.-X., et al. (2020). Sodium tanshinone II sulfonate A ameliorates hypoxia-induced pulmonary hypertension. Front. Pharmacol. 11, 687. doi:10.3389/fphar.2020.00687

PubMed Abstract | CrossRef Full Text | Google Scholar

Bao, C., Liang, S., Han, Y., Yang, Z., Liu, S., Sun, Y., et al. (2023). The novel lysosomal autophagy inhibitor (ROC-325) ameliorates experimental pulmonary hypertension. Hypertension 80, 70–83. doi:10.1161/HYPERTENSIONAHA.122.19397

PubMed Abstract | CrossRef Full Text | Google Scholar

Beik, A., Najafipour, H., Joukar, S., Rajabi, S., Iranpour, M., and Kordestani, Z. (2021). Perillyl alcohol suppresses monocrotaline-induced pulmonary arterial hypertension in rats via anti-remodeling, anti-oxidant, and anti-inflammatory effects. Clin. Exp. Hypertens. 43, 270–280. doi:10.1080/10641963.2020.1860080

PubMed Abstract | CrossRef Full Text | Google Scholar

Burger, C. D., DuBrock, H. M., Cartin-Ceba, R., Moss, J. E., Shapiro, B. P., and Frantz, R. P. (2021). Topic-based, recent literature review on pulmonary hypertension. Mayo Clin. Proc. 96, 3109–3121. doi:10.1016/j.mayocp.2021.05.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Cai, S., Wu, L., Yuan, S., Liu, G., Wang, Y., Fang, L., et al. (2021). Carvacrol alleviates liver fibrosis by inhibiting TRPM7 and modulating the MAPK signaling pathway. Eur. J. Pharmacol. 898, 173982. doi:10.1016/j.ejphar.2021.173982

PubMed Abstract | CrossRef Full Text | Google Scholar

Cao, X., Ma, R., Wang, Y., Huang, Y., You, K., Zhang, L., et al. (2025). Paeoniflorin protects the vascular endothelial barrier in mice with sepsis by activating RXRα signaling. Phytomedicine 138, 156384. doi:10.1016/j.phymed.2025.156384

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, J., Jiang, Q.-D., Chai, Y.-P., Zhang, H., Peng, P., and Yang, X.-X. (2016). Natural terpenes as penetration enhancers for transdermal drug delivery. Molecules 21, 1709. doi:10.3390/molecules21121709

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, G., Fan, M., Liu, Y., Sun, B., Liu, M., Wu, J., et al. (2019). Advances in MS based strategies for probing ligand-target interactions: focus on soft ionization mass spectrometric techniques. Front. Chem. 7, 703. doi:10.3389/fchem.2019.00703

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, T. C., da Fonseca, C. O., Levin, D., and Schönthal, A. H. (2021). The monoterpenoid perillyl alcohol: anticancer agent and medium to overcome biological barriers. Pharmaceutics 13, 2167. doi:10.3390/pharmaceutics13122167

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, X., Chen, Y., Xie, S., Wang, X., Wu, Y., Zhang, H., et al. (2022). The mechanism of Renshen-Fuzi herb pair for treating heart failure-integrating a cardiovascular pharmacological assessment with serum metabolomics. Front. Pharmacol. 13, 995796. doi:10.3389/fphar.2022.995796

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, M., Hu, Q., Wang, S., Tao, L., Hu, X., and Shen, X. (2023). 1,8-Cineole ameliorates endothelial injury and hypertension induced by L-NAME through regulation of autophagy via PI3K/mTOR signaling pathway. Eur. J. Pharmacol. 954, 175863. doi:10.1016/j.ejphar.2023.175863

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, J., Zhang, Z., Huang, M., Yan, J., Gao, R., Cui, J., et al. (2024). Ginsenoside Rg1 prevents and treats acute pulmonary injury induced by high-altitude hypoxia. Int. J. Mol. Sci. 25, 12051. doi:10.3390/ijms252212051

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheng, D., Xiao, J. J., Cheng, H., Liu, Z., Covey, J., and Chan, K. (2005). Analytical method development and pharmacokinetics studies with parthenolide (NSC 157035) and a water-soluble analog (NSC 734325). Cancer Res. Available online at: https://www.semanticscholar.org/paper/Analytical-method-development-and-pharmacokinetics-Cheng-Xiao/faa311f9f6dab8770172892036ad9e5b099dfd03 (Accessed December 4, 2025).

Google Scholar

Cui, C., Yang, R., Chen, H., Li, D., Sun, X., Wang, Y., et al. (2025). Air toxins disorder the NF-kB pathway leads to immune disorders and immune diseases in the human health. Ecotoxicol. Environ. Saf. 302, 118474. doi:10.1016/j.ecoenv.2025.118474

PubMed Abstract | CrossRef Full Text | Google Scholar

Da Fonseca, C. O., Teixeira, R. M., Silva, J. C. T., De Saldanha Da Gama Fischer, J., Meirelles, O. C., Landeiro, J. A., et al. (2013). Long-term outcome in patients with recurrent malignant glioma treated with Perillyl alcohol inhalation. Anticancer Res. 33, 5625–5631.

PubMed Abstract | Google Scholar

Dang, J.-W., Lei, X.-P., Li, Q.-P., and Dong, W.-B. (2019). Asiaticoside attenuates hyperoxia-induced lung injury in vitro and in vivo. Iran. J. Basic Med. Sci. 22, 797–805. doi:10.22038/ijbms.2019.35913.8556

PubMed Abstract | CrossRef Full Text | Google Scholar

Deng, J., Wei, R.-Q., Zhang, W.-M., Shi, C.-Y., Yang, R., Jin, M., et al. (2024). Crocin’s role in modulating MMP2/TIMP1 and mitigating hypoxia-induced pulmonary hypertension in mice. Sci. Rep. 14, 12716. doi:10.1038/s41598-024-62900-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Dianat, M., Radan, M., Mard, S. A., Sohrabi, F., and Saryazdi, S. S. N. (2020). Contribution of reactive oxygen species via the OXR1 signaling pathway in the pathogenesis of monocrotaline-induced pulmonary arterial hypertension: the protective role of Crocin. Life Sci. 256, 117848. doi:10.1016/j.lfs.2020.117848

PubMed Abstract | CrossRef Full Text | Google Scholar

Ding, R., Xie, H., Zhang, Y., Qin, L., Peng, G., Yi, J., et al. (2025). Ginsenoside Rg1 ameliorates pulmonary hypertension by inhibiting cGAS/STING mediated cell senescence. Drug Des. Devel. Ther. 19, 6487–6504. doi:10.2147/DDDT.S527938

PubMed Abstract | CrossRef Full Text | Google Scholar

Dosoky, N. S., and Setzer, W. N. (2018). Chemical composition and biological activities of essential oils of curcuma species. Nutrients 10, 1196. doi:10.3390/nu10091196

PubMed Abstract | CrossRef Full Text | Google Scholar

El-Baba, C., Baassiri, A., Kiriako, G., Dia, B., Fadlallah, S., Moodad, S., et al. (2021). Terpenoids’ anti-cancer effects: focus on autophagy. Apoptosis 26, 491–511. doi:10.1007/s10495-021-01684-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Erdmann, J., Kujaciński, M., and Wiciński, M. (2021). Beneficial effects of ursolic acid and its derivatives-focus on potential biochemical mechanisms in cardiovascular conditions. Nutrients 13, 3900. doi:10.3390/nu13113900

PubMed Abstract | CrossRef Full Text | Google Scholar

Fadón-Padilla, L., Miranda-Pérez de Alejo, C., Miguel-Coello, A. B., Beraza, M., Di Silvio, D., Urkola-Arsuaga, A., et al. (2024). Magnetic nanoradiotracers for targeted neutrophil detection in pulmonary arterial hypertension. J. Nanobiotechnology 22, 709. doi:10.1186/s12951-024-03000-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Freund, R. R. A., Gobrecht, P., Fischer, D., and Arndt, H.-D. (2020). Advances in chemistry and bioactivity of parthenolide. Nat. Prod. Rep. 37, 541–565. doi:10.1039/c9np00049f

PubMed Abstract | CrossRef Full Text | Google Scholar

Fu, K., Feng, C., Shao, L., Mei, L., and Cao, R. (2021). Tanshinone IIA exhibits anti-inflammatory and antioxidative effects in LPS-stimulated bovine endometrial epithelial cells by activating the Nrf2 signaling pathway. Res. Vet. Sci. 136, 220–226. doi:10.1016/j.rvsc.2021.03.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, X., Zhang, Z., Li, X., Wei, Q., Li, H., Li, C., et al. (2020). Ursolic acid improves monocrotaline-induced right ventricular remodeling by regulating metabolism. J. Cardiovasc. Pharmacol. 75, 545–555. doi:10.1097/FJC.0000000000000815

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, J., Hou, D., Hu, P., and Mao, G. (2021). Curcumol increases the sensitivity of colon cancer to 5-FU by regulating Wnt/β-catenin signaling. Transl. Cancer Res. 10, 2437–2450. doi:10.21037/tcr-21-689

PubMed Abstract | CrossRef Full Text | Google Scholar

Gao, J., Li, C., Wang, X., Sun, X., Zhang, R., Chen, C., et al. (2022). Oridonin attenuates lung inflammation and fibrosis in silicosis via covalent targeting iNOS. Biomed. Pharmacother 153, 113532. doi:10.1016/j.biopha.2022.113532

PubMed Abstract | CrossRef Full Text | Google Scholar

Gong, L., Yin, J., Zhang, Y., Huang, R., Lou, Y., Jiang, H., et al. (2022). Neuroprotective mechanisms of ginsenoside Rb1 in central nervous system diseases. Front. Pharmacol. 13, 914352. doi:10.3389/fphar.2022.914352

PubMed Abstract | CrossRef Full Text | Google Scholar

Gu, Y., Liang, Z., Wang, H., Jin, J., Zhang, S., Xue, S., et al. (2016). Tanshinone IIA protects H9c2 cells from oxidative stress-induced cell death via microRNA-133 upregulation and Akt activation. Exp. Ther. Med. 12, 1147–1152. doi:10.3892/etm.2016.3400

PubMed Abstract | CrossRef Full Text | Google Scholar

Gu, C., Yang, Z., Su, S., Ma, K., Nan, X., Li, Z., et al. (2023). 4-Terpineol attenuates pulmonary vascular remodeling via suppressing PI3K/Akt signaling pathway in hypoxia-induced pulmonary hypertension rats. Toxicol. Appl. Pharmacol. 473, 116596. doi:10.1016/j.taap.2023.116596

PubMed Abstract | CrossRef Full Text | Google Scholar

Guo, R., Li, L., Su, J., Li, S., Duncan, S. E., Liu, Z., et al. (2020). Pharmacological activity and mechanism of tanshinone IIA in related diseases. Drug Des. Devel. Ther. 14, 4735–4748. doi:10.2147/DDDT.S266911

PubMed Abstract | CrossRef Full Text | Google Scholar

Han, M., and Fang, X.-L. (2006). Difference in oral absorption of ginsenoside Rg1 between in vitro and in vivo models. Acta Pharmacol. Sin. 27, 499–505. doi:10.1111/j.1745-7254.2006.00303.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Han, J., Tan, C., Pan, Y., Qu, C., Wang, Z., Wang, S., et al. (2023). Andrographolide inhibits the proliferation and migration of vascular smooth muscle cells via PI3K/AKT signaling pathway and amino acid metabolism to prevent intimal hyperplasia. Eur. J. Pharmacol. 959, 176082. doi:10.1016/j.ejphar.2023.176082

PubMed Abstract | CrossRef Full Text | Google Scholar

Hasan, S. K., Jayakumar, S., Espina Barroso, E., Jha, A., Catalano, G., Sandur, S. K., et al. (2025). Molecular targets of oxidative stress: focus on nuclear factor erythroid 2-Related factor 2 function in leukemia and other cancers. Cells 14, 713. doi:10.3390/cells14100713

PubMed Abstract | CrossRef Full Text | Google Scholar

He, Y., Zhong, J.-H., Wei, X.-D., Huang, C.-Y., Peng, P.-L., Yao, J., et al. (2022). Pachymic acid ameliorates pulmonary hypertension by regulating Nrf2-Keap1-ARE pathway. Curr. Med. Sci. 42, 56–67. doi:10.1007/s11596-021-2414-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Hoshino, Y., and Villanueva, L. (2023). Four billion years of microbial terpenome evolution. FEMS Microbiol. Rev. 47, fuad008. doi:10.1093/femsre/fuad008

PubMed Abstract | CrossRef Full Text | Google Scholar

Hou, C.-Y., Hazeena, S. H., Hsieh, S.-L., Li, B.-H., Chen, M.-H., Wang, P.-Y., et al. (2022). Effect of D-Limonene nanoemulsion Edible film on Banana (Musa sapientum Linn.) post-harvest preservation. Molecules 27, 6157. doi:10.3390/molecules27196157

PubMed Abstract | CrossRef Full Text | Google Scholar

Hsu, Y.-H., Hsu, Y.-L., Liu, S.-H., Liao, H.-C., Lee, P.-X., Lin, C.-H., et al. (2016). Development of a bifunctional andrographolide-based chemical probe for pharmacological study. PLoS One 11, e0152770. doi:10.1371/journal.pone.0152770

PubMed Abstract | CrossRef Full Text | Google Scholar

Hu, Y., Chi, L., Kuebler, W. M., and Goldenberg, N. M. (2020). Perivascular inflammation in pulmonary arterial hypertension. Cells 9, 2338. doi:10.3390/cells9112338

PubMed Abstract | CrossRef Full Text | Google Scholar

Huang, C. R., Wang, G. J., Wu, X. L., Li, H., Xie, H. T., Lv, H., et al. (2006). Absorption enhancement study of astragaloside IV based on its transport mechanism in caco-2 cells. Eur. J. Drug Metab. Pharmacokinet. 31, 5–10. doi:10.1007/BF03190635

PubMed Abstract | CrossRef Full Text | Google Scholar

Humbert, M., Morrell, N. W., Archer, S. L., Stenmark, K. R., MacLean, M. R., Lang, I. M., et al. (2004). Cellular and molecular pathobiology of pulmonary arterial hypertension. J. Am. Coll. Cardiol. 43, 13S–24S. doi:10.1016/j.jacc.2004.02.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Igarashi-Sugimoto, A., Tsujino, I., Shima, H., Nakamura, J., Nakaya, T., Sato, T., et al. (2025). Reduced hemoglobin-corrected diffusing capacity in pulmonary arterial hypertension with preserved pulmonary function and morphology. Respir. Investig. 63, 600–607. doi:10.1016/j.resinv.2025.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Ingber, D., Fujita, T., Kishimoto, S., Sudo, K., Kanamaru, T., Brem, H., et al. (1990). Synthetic analogues of fumagillin that inhibit angiogenesis and suppress tumour growth. Nature 348, 555–557. doi:10.1038/348555a0

PubMed Abstract | CrossRef Full Text | Google Scholar

Isbrucker, R. A., and Burdock, G. A. (2006). Risk and safety assessment on the consumption of Licorice root (Glycyrrhiza sp.), its extract and powder as a food ingredient, with emphasis on the pharmacology and toxicology of glycyrrhizin. Regul. Toxicol. Pharmacol. RTP 46, 167–192. doi:10.1016/j.yrtph.2006.06.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Jain, P. P., Zhao, T., Xiong, M., Song, S., Lai, N., Zheng, Q., et al. (2021). Halofuginone, a promising drug for treatment of pulmonary hypertension. Br. J. Pharmacol. 178, 3373–3394. doi:10.1111/bph.15442

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiao, H., and Jia, J. (2022). Ginsenoside compound K acts via LRP1 to alleviate amyloid β42-induced neuroinflammation in microglia by suppressing NF-κB. Biochem. Biophys. Res. Commun. 590, 14–19. doi:10.1016/j.bbrc.2021.12.071

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiao, Q., Xu, X., Xu, L., Wang, Y., Pang, S., Hao, J., et al. (2025). Knockdown of eIF3a alleviates pulmonary arterial hypertension by inhibiting endothelial-to-mesenchymal transition via TGFβ1/SMAD pathway. J. Transl. Med. 23, 524. doi:10.1186/s12967-025-06505-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Jin, H., Jiao, Y., Guo, L., Ma, Y., Zhao, R., Li, X., et al. (2021). Astragaloside IV blocks monocrotaline-induced pulmonary arterial hypertension by improving inflammation and pulmonary artery remodeling. Int. J. Mol. Med. 47, 595–606. doi:10.3892/ijmm.2020.4813

PubMed Abstract | CrossRef Full Text | Google Scholar

Johnson, A. L., Verbitsky, R., Hudson, J., Dean, R., and Hamilton, T. J. (2023). Cannabinoid type-2 receptors modulate terpene induced anxiety-reduction in zebrafish. Biomed. Pharmacother. 168, 115760. doi:10.1016/j.biopha.2023.115760

PubMed Abstract | CrossRef Full Text | Google Scholar

Juergens, L. J., Worth, H., and Juergens, U. R. (2020). New perspectives for mucolytic, anti-inflammatory and adjunctive therapy with 1,8-Cineole in COPD and asthma: review on the new therapeutic approach. Adv. Ther. 37, 1737–1753. doi:10.1007/s12325-020-01279-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Kadsanit, N., Worsawat, P., Sakonsinsiri, C., McElroy, C. R., Macquarrie, D., Noppawan, P., et al. (2024). Sustainable methods for the carboxymethylation and methylation of ursolic acid with dimethyl carbonate under mild and acidic conditions. RSC Adv. 14, 16921–16934. doi:10.1039/d4ra02122c

PubMed Abstract | CrossRef Full Text | Google Scholar

Kannaiyan, R., Shanmugam, M. K., and Sethi, G. (2011). Molecular targets of celastrol derived from thunder of god Vine: potential role in the treatment of inflammatory disorders and cancer. Cancer Lett. 303, 9–20. doi:10.1016/j.canlet.2010.10.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Karkale, S., Khurana, A., Saifi, M. A., Godugu, C., and Talla, V. (2018). Andrographolide ameliorates silica induced pulmonary fibrosis. Int. Immunopharmacol. 62, 191–202. doi:10.1016/j.intimp.2018.07.012

PubMed Abstract | CrossRef Full Text | Google Scholar

Kass, D. J., Rattigan, E., Kahloon, R., Loh, K., Yu, L., Savir, A., et al. (2012). Early treatment with fumagillin, an inhibitor of methionine aminopeptidase-2, prevents pulmonary hypertension in monocrotaline-injured rats. PLoS One 7, e35388. doi:10.1371/journal.pone.0035388

PubMed Abstract | CrossRef Full Text | Google Scholar

Kawade, A., Yamamura, A., Kondo, R., Suzuki, Y., and Yamamura, H. (2023). Corosolic acid ameliorates vascular remodeling in pulmonary arterial hypertension via the downregulation of STAT3 signaling. J. Pharmacol. Sci. 151, 119–127. doi:10.1016/j.jphs.2022.12.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Khazdair, M. R., Moshtagh, M., Anaeigoudari, A., Jafari, S., and Kazemi, T. (2024). Protective effects of carvacrol on lipid profiles, oxidative stress, hypertension, and cardiac dysfunction - a comprehensive review. Food Sci. Nutr. 12, 3137–3149. doi:10.1002/fsn3.4014

PubMed Abstract | CrossRef Full Text | Google Scholar

Khosravi, A. R., and Erle, D. J. (2016). Chitin-induced airway epithelial cell innate immune responses are inhibited by carvacrol/thymol. PLoS One 11, e0159459. doi:10.1371/journal.pone.0159459

PubMed Abstract | CrossRef Full Text | Google Scholar

Kim, Y. W., Kim, M. J., Chung, B. Y., Bang, D. Y., Lim, S. K., Choi, S. M., et al. (2013). Safety evaluation and risk assessment of d-Limonene. J. Toxicol. Environ. 16, 17–38. doi:10.1080/10937404.2013.769418

PubMed Abstract | CrossRef Full Text | Google Scholar

Koçak, S., Kalkan, K. T., Aydın, Ö. S., and Öztürk, K. (2025). Cardioprotective effects of carvacrol in the isoproterenol-induced myocardial infarction model. BMC Pharmacol. Toxicol. 26, 132. doi:10.1186/s40360-025-00967-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Kordestani, Z., Beik, A., Najafipour, H., Safi, Z., Askaripour, M., and Rajabi, S. (2024). Perillyl alcohol, quercetin, and berberine combination therapy ameliorates experimental pulmonary arterial hypertension: effects on the lung miR-204 expression, remodeling, and inflammatory factors. Avicenna J. Phytomedicine 14, 764–775. doi:10.22038/AJP.2024.24522

PubMed Abstract | CrossRef Full Text | Google Scholar

Kurosawa, R., Satoh, K., Kikuchi, N., Kikuchi, H., Saigusa, D., Al-Mamun, M. E., et al. (2019). Identification of celastramycin as a novel therapeutic agent for pulmonary arterial hypertension. Circ. Res. 125, 309–327. doi:10.1161/CIRCRESAHA.119.315229

PubMed Abstract | CrossRef Full Text | Google Scholar

Kurosawa, R., Satoh, K., Nakata, T., Shindo, T., Kikuchi, N., Satoh, T., et al. (2021). Identification of celastrol as a novel therapeutic agent for pulmonary arterial hypertension and right ventricular failure through suppression of bsg (Basigin)/CyPA (Cyclophilin A). Arterioscler. Thromb. Vasc. Biol. 41, 1205–1217. doi:10.1161/ATVBAHA.120.315731

PubMed Abstract | CrossRef Full Text | Google Scholar

Langleben, D., Orfanos, S. E., Fox, B. D., Messas, N., Giovinazzo, M., and Catravas, J. D. (2022). The paradox of pulmonary vascular resistance: restoration of pulmonary capillary recruitment as a sine qua non for true therapeutic success in pulmonary arterial hypertension. J. Clin. Med. 11, 4568. doi:10.3390/jcm11154568

PubMed Abstract | CrossRef Full Text | Google Scholar

Leng, B., Tang, F., Lu, M., Zhang, Z., Wang, H., and Zhang, Y. (2018). Astragaloside IV improves vascular endothelial dysfunction by inhibiting the TLR4/NF-κB signaling pathway. Life Sci. 209, 111–121. doi:10.1016/j.lfs.2018.07.053

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X., Zhang, C.-T., Ma, W., Xie, X., and Huang, Q. (2021). Oridonin: a review of its pharmacology, pharmacokinetics and toxicity. Front. Pharmacol. 12, 645824. doi:10.3389/fphar.2021.645824

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, C., Zhu, H., Zhang, S., Meng, F., Li, S., Li, G., et al. (2022). Astragaloside IV ameliorates pulmonary vascular remodeling in hypoxia-induced pulmonary hypertension by restraining the T follicular helper cell response and expanding T follicular regulatory cell response. Phytomedicine 102, 154171. doi:10.1016/j.phymed.2022.154171

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H., Liu, Q., Yue, Y., Wang, S., Huang, S., Huang, L., et al. (2022a). Celastrol attenuates the remodeling of pulmonary vascular and right ventricular in monocrotaline-induced pulmonary arterial hypertension in rats. Cardiovasc. Diagn. Ther. 12, 88–102. doi:10.21037/cdt-21-360

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, H., Wu, M., Guo, C., Zhai, R., and Chen, J. (2022b). Tanshinone IIA regulates Keap1/Nrf2 signal pathway by activating Sestrin2 to restrain pulmonary fibrosis. Am. J. Chin. Med. 50, 2125–2151. doi:10.1142/S0192415X22500914

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, J., Li, R., Wu, X., Zheng, C., Shiu, P. H.-T., Rangsinth, P., et al. (2022). An update on the potential application of herbal medicine in promoting angiogenesis. Front. Pharmacol. 13, 928817. doi:10.3389/fphar.2022.928817

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, M., Xie, F., Wang, L., Zhu, G., Qi, L.-W., and Jiang, S. (2022). Celastrol: an update on its hepatoprotective properties and the linked molecular mechanisms. Front. Pharmacol. 13, 857956. doi:10.3389/fphar.2022.857956

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X., Yuan, W., Wu, J., Zhen, J., Sun, Q., and Yu, M. (2022). Andrographolide, a natural anti-inflammatory agent: an update. Front. Pharmacol. 13, 920435. doi:10.3389/fphar.2022.920435

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, Z., Zhang, J., Duan, X., Zhao, G., and Zhang, M. (2022). Celastrol: a promising agent fighting against cardiovascular diseases. Antioxid. Basel Switz. 11, 1597. doi:10.3390/antiox11081597

PubMed Abstract | CrossRef Full Text | Google Scholar

Li, X., Sun, C., Zhang, J., Hu, L., Yu, Z., Zhang, X., et al. (2023). Protective effects of paeoniflorin on cardiovascular diseases: a pharmacological and mechanistic overview. Front. Pharmacol. 14, 1122969. doi:10.3389/fphar.2023.1122969

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Z. Q., Jiang, Z. H., Liu, L., and Hu, M. (2006). Mechanisms responsible for poor oral bioavailability of paeoniflorin: role of intestinal disposition and interactions with sinomenine. Pharm. Res. 23, 2768–2780. doi:10.1007/s11095-006-9100-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, T., Xie, L., Liu, H.-M., and Liu, B. (2021). The effects of ginsenoside compound K on PDGF-BB-Induced PASMCs proliferation and phenotypic conversion of pulmonary arterial smooth muscle cells. Sichuan Da Xue Xue Bao Yi Xue Ban. 52, 643–648. doi:10.12182/20210760101

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, B., Peng, Y., Yi, D., Machireddy, N., Dong, D., Ramirez, K., et al. (2022). Endothelial PHD2 deficiency induces nitrative stress via suppression of caveolin-1 in pulmonary hypertension. Eur. Respir. J. 60, 2102643. doi:10.1183/13993003.02643-2021

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J., Fan, G., Tao, N., Feng, F., Meng, C., and Sun, T. (2022). Ginsenoside Rb1 alleviates bleomycin-induced pulmonary inflammation and fibrosis by suppressing central nucleotide-binding oligomerization-leucine-rich repeat-and pyrin domains-containing protein three inflammasome activation and the NF-κB pathway. Drug Des. Devel. Ther. 16, 1793–1809. doi:10.2147/DDDT.S361748

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, H., Wang, S., Chen, Q., Ge, X., Ning, H., Guo, Y., et al. (2023). Natural targeting potent ROS-eliminating tungsten-based polyoxometalate nanodots for efficient treatment of pulmonary hypertension. Adv. Healthc. Mater. 12, e2300252. doi:10.1002/adhm.202300252

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Y., Tang, B.-L., Lu, M.-L., and Wang, H.-X. (2023). Astragaloside IV improves pulmonary arterial hypertension by increasing the expression of CCN1 and activating the ERK1/2 pathway. J. Cell. Mol. Med. 27, 622–633. doi:10.1111/jcmm.17681

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, Z., Wang, J., Jin, X., Gao, P., Zhao, Y., Yin, M., et al. (2023). 1,8-Cineole alleviates OGD/R-Induced oxidative damage and restores mitochondrial function by promoting the Nrf2 pathway. Biol. Pharm. Bull. 46, 1371–1384. doi:10.1248/bpb.b23-00154

PubMed Abstract | CrossRef Full Text | Google Scholar

Luo, Y., Xu, D.-Q., Dong, H.-Y., Zhang, B., Liu, Y., Niu, W., et al. (2013). Tanshinone IIA inhibits hypoxia-induced pulmonary artery smooth muscle cell proliferation via Akt/Skp2/p27-associated pathway. PLoS One 8, e56774. doi:10.1371/journal.pone.0056774

PubMed Abstract | CrossRef Full Text | Google Scholar

Masson, B., Le Ribeuz, H., Sabourin, J., Laubry, L., Woodhouse, E., Foster, R., et al. (2022). Orai1 inhibitors as potential treatments for pulmonary arterial hypertension. Circ. Res. 131, e102–e119. doi:10.1161/CIRCRESAHA.122.321041

PubMed Abstract | CrossRef Full Text | Google Scholar

Mathur, A., Meena, A., and Luqman, S. (2024). Monoterpenoids: an upcoming class of therapeutic agents for modulating cancer metastasis. Phytother. Res. 38, 939–969. doi:10.1002/ptr.8081

PubMed Abstract | CrossRef Full Text | Google Scholar

McLean, S., Boyle, R. R., Brandon, S., Davies, N. W., and Sorensen, J. S. (2007). Pharmacokinetics of 1,8-cineole, a dietary toxin, in the brushtail possum (Trichosurus vulpecula): significance for feeding. Xenobiotica 37, 903–922. doi:10.1080/00498250701570277

PubMed Abstract | CrossRef Full Text | Google Scholar

Mondéjar-Parreño, G., Cogolludo, A., and Perez-Vizcaino, F. (2021). Potassium (K+) channels in the pulmonary vasculature: implications in pulmonary hypertension physiological, pathophysiological and pharmacological regulation. Pharmacol. Ther. 225, 107835. doi:10.1016/j.pharmthera.2021.107835

PubMed Abstract | CrossRef Full Text | Google Scholar

Morris, H. E., Neves, K. B., Nilsen, M., Montezano, A. C., MacLean, M. R., and Touyz, R. M. (2023). Notch3/Hes5 induces vascular dysfunction in hypoxia-induced pulmonary hypertension through ER stress and redox-sensitive pathways. Hypertens 80, 1683–1696. doi:10.1161/HYPERTENSIONAHA.122.20449

PubMed Abstract | CrossRef Full Text | Google Scholar

Nie, X., Shen, C., Tan, J., Yang, X., Wang, W., Dai, Y., et al. (2021). Andrographolide attenuates established pulmonary hypertension via rescue of vascular remodeling. Biomolecules 11, 1801. doi:10.3390/biom11121801

PubMed Abstract | CrossRef Full Text | Google Scholar

Nie, X., Wu, Z., Shang, J., Zhu, L., Liu, Y., and Qi, Y. (2023). Curcumol suppresses endothelial-to-mesenchymal transition via inhibiting the AKT/GSK3β signaling pathway and alleviates pulmonary arterial hypertension in rats. Eur. J. Pharmacol. 943, 175546. doi:10.1016/j.ejphar.2023.175546

PubMed Abstract | CrossRef Full Text | Google Scholar

Niu, L.-C., Zhang, R., Qi, Q., Tang, B.-L., Yu, S.-X., Wang, G., et al. (2025). Astragaloside IV improves pulmonary vascular endothelial dysfunction in pulmonary arterial hypertension by inhibiting ferroptosis through modulation of the Calpain-1/TGF-β/TFRC pathway. Am. J. Chin. Med. 53, 1181–1206. doi:10.1142/S0192415X25500454

PubMed Abstract | CrossRef Full Text | Google Scholar

Nozohour, Y., Maham, M., and Dalir-Naghadeh, B. (2022). Spasmolytic effect of 1,8 cineole is mediated through calcium channel blockade in the bovine ileum. Vet. Res. Forum. 13, 357–362. doi:10.30466/vrf.2021.528973.3171

PubMed Abstract | CrossRef Full Text | Google Scholar

Oliveira, J. R., Ribeiro, G. H. M., Rezende, L. F., and Fraga-Silva, R. A. (2021). Plant terpenes on treating cardiovascular and metabolic disease: a review. Protein Pept. Lett. 28, 750–760. doi:10.2174/0929866528999210128210145

PubMed Abstract | CrossRef Full Text | Google Scholar

Othman, N. S., and Mohd Azman, D. K. (2022). Andrographolide induces G2/M cell cycle arrest and apoptosis in human glioblastoma DBTRG-05MG cell line via ERK1/2/c-Myc/p53 signaling pathway. Molecules 27, 6686. doi:10.3390/molecules27196686

PubMed Abstract | CrossRef Full Text | Google Scholar

Pan, Y., Tiong, K. H., Abd-Rashid, B. A., Ismail, Z., Ismail, R., Mak, J. W., et al. (2014). In vitro effect of important herbal active constituents on human cytochrome P450 1A2 (CYP1A2) activity. Phytomedicine 21, 1645–1650. doi:10.1016/j.phymed.2014.08.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Pereira-Gonçalves, Á., Ferreira-da-Silva, F. W., de Holanda-Angelin-Alves, C. M., Cardoso-Teixeira, A. C., Coelho-de-Souza, A. N., and Leal-Cardoso, J. H. (2018). 1,8-Cineole blocks voltage-gated L-type calcium channels in tracheal smooth muscle. Pflugers Arch. 470, 1803–1813. doi:10.1007/s00424-018-2201-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Poyatos, P., Gratacós, M., Samuel, K., Orriols, R., and Tura-Ceide, O. (2023). Oxidative stress and antioxidant therapy in pulmonary hypertension. Antioxid. Basel Switz. 12, 1006. doi:10.3390/antiox12051006

PubMed Abstract | CrossRef Full Text | Google Scholar

Puppala, E. R., Aochenlar, S. L., Shantanu, P. A., Ahmed, S., Jannu, A. K., Jala, A., et al. (2022). Perillyl alcohol attenuates chronic restraint stress aggravated dextran sulfate sodium-induced ulcerative colitis by modulating TLR4/NF-κB and JAK2/STAT3 signaling pathways. Phytomedicine 106, 154415. doi:10.1016/j.phymed.2022.154415

PubMed Abstract | CrossRef Full Text | Google Scholar

Qian, G., Cao, J., Chen, C., Wang, L., Huang, X., Ding, C., et al. (2013). Paeoniflorin inhibits pulmonary artery smooth muscle cells proliferation via upregulating A2B adenosine receptor in rat. PloS One 8, e69141. doi:10.1371/journal.pone.0069141

PubMed Abstract | CrossRef Full Text | Google Scholar

Qing, C., Ziyun, L., Xuefei, Y., Xinyi, Z., Xindong, X., and Jianhua, F. (2022). Protective effects of 18β-Glycyrrhetinic acid on neonatal rats with hyperoxia exposure. Inflammation 45, 1224–1238. doi:10.1007/s10753-021-01616-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Qiu, F., Zeng, J., Liu, S., He, M., Zhu, L., Ye, Y., et al. (2014). Effects of danshen ethanol extract on the pharmacokinetics of fexofenadine in healthy volunteers. Evid.-Based Complement. Altern. Med. ECAM 2014, 473213. doi:10.1155/2014/473213

PubMed Abstract | CrossRef Full Text | Google Scholar

Rajabi, S., Najafipour, H., Jafarinejad Farsangi, S., Joukar, S., Beik, A., Iranpour, M., et al. (2020). Perillyle alcohol and Quercetin ameliorate monocrotaline-induced pulmonary artery hypertension in rats through PARP1-mediated miR-204 down-regulation and its downstream pathway. BMC Complement. Med. Ther. 20, 218. doi:10.1186/s12906-020-03015-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Rajabi, S., Najafipour, H., Jafarinejad-Farsangi, S., Joukar, S., Beik, A., Askaripour, M., et al. (2021). Quercetin, perillyl alcohol, and berberine ameliorate right ventricular disorders in experimental pulmonary arterial hypertension: effects on miR-204, miR-27a, fibrotic, apoptotic, and inflammatory factors. J. Cardiovasc. Pharmacol. 77, 777–786. doi:10.1097/FJC.0000000000001015

PubMed Abstract | CrossRef Full Text | Google Scholar

Rakoczy, K., Szymańska, N., Stecko, J., Kisiel, M., Maruszak, M., Niedziela, M., et al. (2025). Applications of limonene in neoplasms and non-neoplastic diseases. Int. J. Mol. Sci. 26, 6359. doi:10.3390/ijms26136359

PubMed Abstract | CrossRef Full Text | Google Scholar

Ran, C., Lu, M., Zhao, F., Hao, Y., Guo, X., Li, Y., et al. (2024). Ginsenoside Rg1 alleviates vascular remodeling in hypoxia-induced pulmonary hypertension mice through the calpain-1/STAT3 signaling pathway. J. Ginseng Res. 48, 405–416. doi:10.1016/j.jgr.2024.03.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Ren, S., Zhang, H., Mu, Y., Sun, M., and Liu, P. (2013). Pharmacological effects of astragaloside IV: a literature review. J. Tradit. Chin. Med. 33, 413–416. doi:10.1016/s0254-6272(13)60189-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Rosa, G. P., Silva, B. J. C., Seca, A. M. L., Moujir, L. M., and Barreto, M. C. (2020). Phytochemicals with added value from morella and myrica species. Molecules 25, 6052. doi:10.3390/molecules25246052

PubMed Abstract | CrossRef Full Text | Google Scholar

Ruffenach, G., Medzikovic, L., Aryan, L., Sun, W., Lertpanit, L., O’Connor, E., et al. (2024). Intestinal IFNα4 promotes 15-HETE diet-induced pulmonary hypertension. Respir. Res. 25, 419. doi:10.1186/s12931-024-03046-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Salehi, B., Gültekin-Özgüven, M., Kırkın, C., Özçelik, B., Morais-Braga, M. F. B., Carneiro, J. N. P., et al. (2019). Anacardium plants: chemical,nutritional composition and biotechnological applications. Biomolecules 9, 465. doi:10.3390/biom9090465

PubMed Abstract | CrossRef Full Text | Google Scholar

Shakya, R., Nepal, M. R., Kang, M. J., and Jeong, T. C. (2020). Effects of intestinal microbiota on pharmacokinetics of crocin and crocetin in male sprague-dawley rats. Metabolites 10, 424. doi:10.3390/metabo10110424

PubMed Abstract | CrossRef Full Text | Google Scholar

Shan, L., Tang, X., Liu, Y., Qi, W., Zhao, H., Zang, L., et al. (2025). Targeting BMPER as a therapeutic strategy for pulmonary arterial hypertension. Cell. Signal. 133, 111880. doi:10.1016/j.cellsig.2025.111880

PubMed Abstract | CrossRef Full Text | Google Scholar

Shanahati, D., Yang, T., Fang, L., Nijiati, Y., Aihemaitituoheti, A., Abudukeremu, A., et al. (2025). 18β-glycyrrhetinic acid improves pulmonary hypertension by regulating the vascular non-inflammatory molecule-1/L-arginine/nitric oxide signaling pathway. Eur. J. Pharmacol. 996, 177382. doi:10.1016/j.ejphar.2025.177382

PubMed Abstract | CrossRef Full Text | Google Scholar

Sharmin, N., Nganwuchu, C. C., and Nasim, M. T. (2021). Targeting the TGF-β signaling pathway for resolution of pulmonary arterial hypertension. Trends Pharmacol. Sci. 42, 510–513. doi:10.1016/j.tips.2021.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Sheng, Y., Gong, X., Zhao, J., Liu, Y., and Yuan, Y. (2022). Effects of crocin on CCL2/CCR2 inflammatory pathway in monocrotaline-induced pulmonary arterial hypertension rats. Am. J. Chin. Med. 50, 241–259. doi:10.1142/S0192415X22500082

PubMed Abstract | CrossRef Full Text | Google Scholar

Silva, E. A. P., Santos, D. M., de Carvalho, F. O., Menezes, I. A. C., Barreto, A. S., Souza, D. S., et al. (2021). Monoterpenes and their derivatives as agents for cardiovascular disease management: a systematic review and meta-analysis. Phytomedicine 88, 153451. doi:10.1016/j.phymed.2020.153451

PubMed Abstract | CrossRef Full Text | Google Scholar

Singh, J., Luqman, S., and Meena, A. (2023). Carvacrol as a prospective regulator of cancer targets/signalling pathways. Curr. Mol. Pharmacol. 16, 542–558. doi:10.2174/1874467215666220705142954

PubMed Abstract | CrossRef Full Text | Google Scholar

Smolders, V. F. E. D., Lodder, K., Rodríguez, C., Tura-Ceide, O., Barberà, J. A., Jukema, J. W., et al. (2021). The inflammatory profile of CTEPH-derived endothelial cells is a possible driver of disease progression. Cells 10, 737. doi:10.3390/cells10040737

PubMed Abstract | CrossRef Full Text | Google Scholar

Sobral, P. J. M., Vicente, A. T. S., and Salvador, J. A. R. (2023). Recent advances in oridonin derivatives with anticancer activity. Front. Chem. 11, 1066280. doi:10.3389/fchem.2023.1066280

PubMed Abstract | CrossRef Full Text | Google Scholar

Stockmann-Juvala, H., and Savolainen, K. (2008). A review of the toxic effects and mechanisms of action of fumonisin B1. Hum. Exp. Toxicol. 27, 799–809. doi:10.1177/0960327108099525

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, J. (2007). D-Limonene: safety and clinical applications. Altern. Med. Rev. J. Clin. Ther. 12, 259–264.

PubMed Abstract | Google Scholar

Sun, Y., Lu, M., Sun, T., and Wang, H. (2021). Astragaloside IV attenuates inflammatory response mediated by NLRP-3/calpain-1 is involved in the development of pulmonary hypertension. J. Cell. Mol. Med. 25, 586–590. doi:10.1111/jcmm.15671

PubMed Abstract | CrossRef Full Text | Google Scholar

Tan, W. S. D., Peh, H. Y., Liao, W., Pang, C. H., Chan, T. K., Lau, S. H., et al. (2016). Cigarette smoke-induced lung disease predisposes to more severe infection with nontypeable haemophilus influenzae: protective effects of andrographolide. J. Nat. Prod. 79, 1308–1315. doi:10.1021/acs.jnatprod.5b01006

PubMed Abstract | CrossRef Full Text | Google Scholar

Tan, J., Cao, X., Zheng, R., Xie, S., Yi, J., Wang, F., et al. (2025). Celastrol ameliorates hypoxia-induced pulmonary hypertension by regulation of the PDE5-cGMP-PKG signaling pathway. Phytother. Res. 39, 1549–1564. doi:10.1002/ptr.8446

PubMed Abstract | CrossRef Full Text | Google Scholar

Tang, B.-L., Liu, Y., Zhang, J.-L., Lu, M.-L., and Wang, H.-X. (2023). Ginsenoside Rg1 ameliorates hypoxia-induced pulmonary arterial hypertension by inhibiting endothelial-to-mesenchymal transition and inflammation by regulating CCN1. Biomed. Pharmacother. 164, 114920. doi:10.1016/j.biopha.2023.114920

PubMed Abstract | CrossRef Full Text | Google Scholar

Tang, Q., Markby, G. R., MacNair, A. J., Tang, K., Tkacz, M., Parys, M., et al. (2023). TGF-β-induced PI3K/AKT/mTOR pathway controls myofibroblast differentiation and secretory phenotype of valvular interstitial cells through the modulation of cellular senescence in a naturally occurring in vitro canine model of myxomatous mitral valve disease. Cell Prolif. 56, e13435. doi:10.1111/cpr.13435

PubMed Abstract | CrossRef Full Text | Google Scholar

Tang, H., Ning, K., Wu, B., Wang, X., He, J., Li, P., et al. (2025). Scutellarein ameliorates pulmonary arterial hypertension via sirtuin 1 mediated deacetylation of nicotinamide nucleotide transhydrogenase. Biochem. Pharmacol. 237, 116932. doi:10.1016/j.bcp.2025.116932

PubMed Abstract | CrossRef Full Text | Google Scholar

Teixeira-Fonseca, J. L., Orts, D. J. B. Y., Silva, P. L. da, Conceição, M. R. de L., Hermes, H., Prudencio, C. R., et al. (2024). In vivo anti-inflammatory activity of D-Limonene in a rat model of monocrotaline-induced pulmonary hypertension: implications to the heart function. Arq. Bras. Cardiol. 121, e20240195. doi:10.36660/abc.20240195

PubMed Abstract | CrossRef Full Text | Google Scholar

Testai, L., Chericoni, S., Martelli, A., Flamini, G., Breschi, M. C., and Calderone, V. (2016). Voltage-operated potassium (Kv) channels contribute to endothelium-dependent vasorelaxation of carvacrol on rat aorta. J. Pharm. Pharmacol. 68, 1177–1183. doi:10.1111/jphp.12585

PubMed Abstract | CrossRef Full Text | Google Scholar

Tian, Q., Liu, J., Chen, Q., and Zhang, M. (2023). Andrographolide contributes to the attenuation of cardiac hypertrophy by suppressing endoplasmic reticulum stress. Pharm. Biol. 61, 61–68. doi:10.1080/13880209.2022.2157021

PubMed Abstract | CrossRef Full Text | Google Scholar

Tossetta, G., Fantone, S., Piani, F., Crescimanno, C., Ciavattini, A., Giannubilo, S. R., et al. (2023). Modulation of NRF2/KEAP1 signaling in preeclampsia. Cells 12, 1545. doi:10.3390/cells12111545

PubMed Abstract | CrossRef Full Text | Google Scholar

Tran, Q. T. N., Tan, W. S. D., Wong, W. S. F., and Chai, C. L. L. (2021). Polypharmacology of andrographolide: beyond one molecule one target. Nat. Prod. Rep. 38, 682–692. doi:10.1039/d0np00049c

PubMed Abstract | CrossRef Full Text | Google Scholar

Vanderpool, R. R., Tang, H., Rischard, F., and Yuan, J. X.-J. (2017). Is p38 MAPK a dark force in right ventricular hypertrophy and failure in pulmonary arterial hypertension? Am. J. Respir. Cell Mol. Biol. 57, 506–508. doi:10.1165/rcmb.2017-0197ED

PubMed Abstract | CrossRef Full Text | Google Scholar

Villegas-Esguevillas, M., Cho, S., Vera-Zambrano, A., Kwon, J. W., Barreira, B., Telli, G., et al. (2023). The novel KV7 channel activator URO-K10 exerts enhanced pulmonary vascular effects independent of the KCNE4 regulatory subunit. Biomed. Pharmacother. Biomedecine Pharmacother. 164, 114952. doi:10.1016/j.biopha.2023.114952

PubMed Abstract | CrossRef Full Text | Google Scholar

Vitry, G., Paulin, R., Grobs, Y., Lampron, M.-C., Shimauchi, T., Lemay, S.-E., et al. (2021). Oxidized DNA precursors cleanup by NUDT1 contributes to vascular remodeling in pulmonary arterial hypertension. Am. J. Respir. Crit. Care Med. 203, 614–627. doi:10.1164/rccm.202003-0627OC

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L.-X., Sun, Y., Chen, C., Huang, X.-Y., Lin, Q., Qian, G.-Q., et al. (2009). Effects and mechanism of oridonin on pulmonary hypertension induced by chronic hypoxia-hypercapnia in rats. Chin. Med. J. (Engl.) 122, 1380–1387.

PubMed Abstract | Google Scholar

Wang, J., Dong, M.-Q., Liu, M.-L., Xu, D.-Q., Luo, Y., Zhang, B., et al. (2010). Tanshinone IIA modulates pulmonary vascular response to agonist and hypoxia primarily via inhibiting Ca2+ influx and release in normal and hypoxic pulmonary hypertension rats. Eur. J. Pharmacol. 640, 129–138. doi:10.1016/j.ejphar.2010.04.047

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, R.-X., He, R.-L., Jiao, H.-X., Dai, M., Mu, Y.-P., Hu, Y., et al. (2015). Ginsenoside Rb1 attenuates agonist-induced contractile response via inhibition of store-operated calcium entry in pulmonary arteries of normal and pulmonary hypertensive rats. Cell. Physiol. Biochem. 35, 1467–1481. doi:10.1159/000373966

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X.-B., Wang, W., Zhu, X.-C., Ye, W.-J., Cai, H., Wu, P.-L., et al. (2015). The potential of asiaticoside for TGF-β1/Smad signaling inhibition in prevention and progression of hypoxia-induced pulmonary hypertension. Life Sci. 137, 56–64. doi:10.1016/j.lfs.2015.07.016

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Cai, X., Wang, W., Jin, Y., Chen, M., Huang, X., et al. (2018a). Effect of asiaticoside on endothelial cells in hypoxia-induced pulmonary hypertension. Mol. Med. Rep. 17, 2893–2900. doi:10.3892/mmr.2017.8254

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Li, G., and Shen, W. (2018b). Protective effects of D-Limonene against transient cerebral ischemia in stroke-prone spontaneously hypertensive rats. Exp. Ther. Med. 15, 699–706. doi:10.3892/etm.2017.5509

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, R.-X., He, R.-L., Jiao, H.-X., Zhang, R.-T., Guo, J.-Y., Liu, X.-R., et al. (2020). Preventive treatment with ginsenoside Rb1 ameliorates monocrotaline-induced pulmonary arterial hypertension in rats and involves store-operated calcium entry inhibition. Pharm. Biol. 58, 1055–1063. doi:10.1080/13880209.2020.1831026

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Duo, D., Yan, Y., He, R., Wang, S., Wang, A., et al. (2020). Extract of Salvia przewalskii repair tissue damage in chronic hypoxia maybe through the RhoA-ROCK signalling pathway. Biol. Pharm. Bull. 43, 432–439. doi:10.1248/bpb.b19-00775

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, C., Xing, Y., Zhang, J., He, M., Dong, J., Chen, S., et al. (2022). MED1 regulates BMP/TGF-β in endothelium: implication for pulmonary hypertension. Circ. Res. 131, 828–841. doi:10.1161/CIRCRESAHA.122.321532

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J.-L., Liu, H., Jing, Z.-C., Zhao, F., and Zhou, R. (2022). 18β-Glycyrrhetinic acid ameliorates endoplasmic reticulum stress-induced inflammation in pulmonary arterial hypertension through PERK/eIF2α/NF-κB signaling. Chin. J. Physiol. 65, 187–198. doi:10.4103/0304-4920.354801

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, R.-R., Yuan, T.-Y., Wang, J.-M., Chen, Y.-C., Zhao, J.-L., Li, M.-T., et al. (2022). Immunity and inflammation in pulmonary arterial hypertension: from pathophysiology mechanisms to treatment perspective. Pharmacol. Res. 180, 106238. doi:10.1016/j.phrs.2022.106238

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, X., Zhang, M., and Li, Y. (2022). Recent studies on the pharmacological activities and structural modifications of Compound-K. Mini Rev. Med. Chem. 22, 2847–2863. doi:10.2174/1389557522666220513120828

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Hu, S., Xu, Y., and Wang, T. (2025). Omega-6 polyunsaturated fatty acids and their metabolites: a potential targeted therapy for pulmonary hypertension. Respir. Res. 26, 102. doi:10.1186/s12931-025-03172-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, L., Liu, T., Liu, B., Wang, X., Zhao, L., and Zhou, T. (2007a). Effect of triptolide on the development of monocrotaline-induced pulmonary hypertension in pneumonectomized rat. Sichuan Da Xue Xue Bao Yi Xue Ban. 38, 806–809.

PubMed Abstract | Google Scholar

Wei, L., Liu, T., Liu, B., Wang, X.-M., Zhao, L., and Zhou, T.-F. (2007b). Effect of triptolide on the expression of matrix metalloproteinases 2 and 9 in lungs of experimental pulmonary hypertension. Zhongguo Dang Dai Er Ke Za Zhi Chin. J. Contemp. Pediatr. 9, 479–483.

PubMed Abstract | Google Scholar

Wei, C., Wang, H., Sun, X., Bai, Z., Wang, J., Bai, G., et al. (2022). Pharmacological profiles and therapeutic applications of pachymic acid. Exp. Ther. Med. 24, 547. (Review). doi:10.3892/etm.2022.11484

PubMed Abstract | CrossRef Full Text | Google Scholar

Wei, J., Fei, Z., Pan, G., Weiss, L. M., and Zhou, Z. (2022). Current therapy and therapeutic targets for microsporidiosis. Front. Microbiol. 13, 835390. doi:10.3389/fmicb.2022.835390

PubMed Abstract | CrossRef Full Text | Google Scholar

Wong, S. K., Chin, K.-Y., and Ima-Nirwana, S. (2021). A review on the molecular basis underlying the protective effects of Andrographis paniculata and andrographolide against myocardial injury. Drug Des. Devel. Ther. 15, 4615–4632. doi:10.2147/DDDT.S331027

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, Q. Q., Ni, J., Zhang, N., Liao, H. H., Tang, Q. Z., and Deng, W. (2017). Andrographolide protects against aortic banding-induced experimental cardiac hypertrophy by inhibiting MAPKs signaling. Front. Pharmacol. 8, 808. doi:10.3389/fphar.2017.00808

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, Q., Du, X., Cheng, J., Qi, X., Liu, H., Lv, X., et al. (2023). PECAM-1 drives β-catenin-mediated EndMT via internalization in colon cancer with diabetes mellitus. Cell Commun. Signal. 21, 203. doi:10.1186/s12964-023-01193-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, J.-J., Zhang, L., Liu, D., Xia, J., Yang, Y., Tang, F., et al. (2024). Ginsenoside Rg1, lights up the way for the potential prevention of Alzheimer’s disease due to its therapeutic effects on the drug-controllable risk factors of Alzheimer’s disease. J. Ethnopharmacol. 318, 116955. doi:10.1016/j.jep.2023.116955

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, M., Li, H., Zhai, R., Shan, B., Guo, C., and Chen, J. (2024). Tanshinone IIA positively regulates the Keap1-Nrf2 system to alleviate pulmonary fibrosis via the sestrin2-sqstm1 signaling axis-mediated autophagy. Phytomedicine 129, 155620. doi:10.1016/j.phymed.2024.155620

PubMed Abstract | CrossRef Full Text | Google Scholar

Xi, C., Peng, S., Wu, Z., Zhou, Q., and Zhou, J. (2017). Toxicity of triptolide and the molecular mechanisms involved. Biomed. Pharmacother. 90, 531–541. doi:10.1016/j.biopha.2017.04.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Xi, S., Li, X., Chen, W., Cao, Y., and Ke, Y. (2025). Crocin-I mitigates diquat-induced pulmonary fibrosis via activation of the SIRT3/FOXO3a pathway. Biomed. Pharmacother. 186, 118043. doi:10.1016/j.biopha.2025.118043

PubMed Abstract | CrossRef Full Text | Google Scholar

XinTian, null, Zhang, X., Feng, Y., Gao, X., Hao, X., Zhang, J., et al. (2022). Astragaloside IV in hypoxic pulmonary hypertension: an in vivo and in vitro experiments. Appl. Biochem. Biotechnol. 194, 6319–6334. doi:10.1007/s12010-022-04027-y

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, H., Mao, X., Nie, Z., and Li, Y. (2023). Oxr1a prevents the premature ovarian failure by regulating oxidative stress and mitochondrial function in zebrafish. Free Radic. Biol. Med. 203, 102–113. doi:10.1016/j.freeradbiomed.2023.04.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Xu, Y., Wang, Y.-R., Peng, W.-P., Bu, H.-M., Zhou, Y., and Wu, Q. (2025). Tanshinone IIA alleviates pulmonary fibrosis by inhibiting pyroptosis of alveolar epithelial cells through the MAPK signaling pathway. Phytother. Res. 39, 282–297. doi:10.1002/ptr.8372

PubMed Abstract | CrossRef Full Text | Google Scholar

Yadav, S., Singh, S., and Singh, M. (2025). Protective effects of Tanshinone IIA preconditioning against hypobaric hypoxia-induced lung injury in a rat model. Naunyn. Schmiedeb. Arch. Pharmacol. 398, 13803–13818. doi:10.1007/s00210-025-04118-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Yamamura, A., Fujiwara, M., Kawade, A., Amano, T., Hossain, A., Nayeem, M. J., et al. (2024). Corosolic acid attenuates platelet-derived growth factor signaling in macrophages and smooth muscle cells of pulmonary arterial hypertension. Eur. J. Pharmacol. 973, 176564. doi:10.1016/j.ejphar.2024.176564

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, L., Zhou, G., Liu, J., Song, J., Zhang, Z., Huang, Q., et al. (2021). Tanshinone I and tanshinone IIA/B attenuate LPS-induced mastitis via regulating the NF-κB. Biomed. Pharmacother. 137, 111353. doi:10.1016/j.biopha.2021.111353

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, T., Zhou, J., Fang, L., Wang, M., Dilinuer, M., and Ainiwaer, A. (2021). Protection function of 18β-glycyrrhetinic acid on rats with high-altitude pulmonary hypertension based on 1H NMR metabonomics technology. Anal. Biochem. 631, 114342. doi:10.1016/j.ab.2021.114342

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, Y.-S., Wen, D., and Zhao, X.-F. (2021). Preventive and therapeutic effect of intraportal oridonin on BALb/c nude mice hemispleen model of colon cancer liver metastasis. Transl. Cancer Res. 10, 1324–1335. doi:10.21037/tcr-20-3042

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, H., Wang, L., Yang, M., Hu, J., Zhang, E., and Peng, L. (2022). Oridonin attenuates LPS-induced early pulmonary fibrosis by regulating impaired autophagy, oxidative stress, inflammation and EMT. Eur. J. Pharmacol. 923, 174931. doi:10.1016/j.ejphar.2022.174931

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, C., Pan, Q., Ji, K., Tian, Z., Zhou, H., Li, S., et al. (2023). Review on the protective mechanism of astragaloside IV against cardiovascular diseases. Front. Pharmacol. 14, 1187910. doi:10.3389/fphar.2023.1187910

PubMed Abstract | CrossRef Full Text | Google Scholar

Yao, J., Fang, X., Zhang, C., Yang, Y., Wang, D., Chen, Q., et al. (2021). Astragaloside IV attenuates hypoxia-induced pulmonary vascular remodeling via the Notch signaling pathway. Mol. Med. Rep. 23, 89. doi:10.3892/mmr.2020.11726

PubMed Abstract | CrossRef Full Text | Google Scholar

Yao, M., Wang, J., Zhang, J., Guo, Y., Ni, Z., Jia, X., et al. (2023). Asiaticoside attenuates oxygen-glucose deprivation/reoxygenation-caused injury of cardiomyocytes by inhibiting autophagy. J. Appl. Toxicol. 43, 789–798. doi:10.1002/jat.4424

PubMed Abstract | CrossRef Full Text | Google Scholar

Yao, Y., Song, L., Zuo, Z., Chen, Z., Wang, Y., Cai, H., et al. (2024). Parthenolide attenuates hypoxia-induced pulmonary hypertension through inhibiting STAT3 signaling. Phytomedicine 134, 155976. doi:10.1016/j.phymed.2024.155976

PubMed Abstract | CrossRef Full Text | Google Scholar

Ye, L., Wang, T., Tang, L., Liu, W., Yang, Z., Zhou, J., et al. (2011). Poor oral bioavailability of a promising anticancer agent andrographolide is due to extensive metabolism and efflux by P-glycoprotein. J. Pharm. Sci. 100, 5007–5017. doi:10.1002/jps.22693

PubMed Abstract | CrossRef Full Text | Google Scholar

Younis, N. S. (2020). D-Limonene mitigate myocardial injury in rats through MAPK/ERK/NF-κB pathway inhibition. Korean J. Physiol. Pharmacol. 24, 259–266. doi:10.4196/kjpp.2020.24.3.259

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, M., Peng, L., Liu, P., Yang, M., Zhou, H., Ding, Y., et al. (2020). Paeoniflorin ameliorates chronic Hypoxia/SU5416-Induced pulmonary arterial hypertension by inhibiting endothelial-to-mesenchymal transition. Drug Des. Devel. Ther. 14, 1191–1202. doi:10.2147/DDDT.S235207

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, W., Zeng, M., Xu, P., Liu, J., and Wang, H. (2021). Effect of paeoniflorin on acute lung injury induced by influenza A virus in mice. Evidences of its mechanism of action. Phytomedicine 92, 153724. doi:10.1016/j.phymed.2021.153724

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, M., Wu, X., Wang, J., He, M., Han, H., Hu, S., et al. (2022). Paeoniflorin attenuates monocrotaline-induced pulmonary arterial hypertension in rats by suppressing TAK1-MAPK/NF-κB pathways. Int. J. Med. Sci. 19, 681–694. doi:10.7150/ijms.69289

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, Z., Xiao, J., Chen, X., Ruan, Y., Chen, Y., Zheng, X., et al. (2022). Bioactivities and mechanisms of natural medicines in the management of pulmonary arterial hypertension. Chin. Med. 17, 13. doi:10.1186/s13020-022-00568-w

PubMed Abstract | CrossRef Full Text | Google Scholar

Yu, Y., Wang, Y., Yang, Z., Li, Z., Lu, D., and Nan, X. (2025). Methyleugenol alleviates pulmonary vascular remodeling in rats with high-altitude pulmonary hypertension by improving pulmonary smooth muscle cell function. Biomed. Pharmacother. 187, 118109. doi:10.1016/j.biopha.2025.118109

PubMed Abstract | CrossRef Full Text | Google Scholar

Zeng, C., Liu, J., Zheng, X., Hu, X., and He, Y. (2023). Prostaglandin and prostaglandin receptors: present and future promising therapeutic targets for pulmonary arterial hypertension. Respir. Res. 24, 263. doi:10.1186/s12931-023-02559-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhai, S., Wang, R., Wang, J., Xu, X., Niu, L., Guo, M., et al. (2024). Curcumol: a review of its pharmacology, pharmacokinetics, drug delivery systems, structure-activity relationships, and potential applications. Inflammopharmacology 32, 1659–1704. doi:10.1007/s10787-024-01447-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X.-Y., and Zhang, Y.-W. (2015). Biotransformation of asiaticoside and asiatic acid by Nocardia sp. BioTechnol. Indian J. 11 (4).

Google Scholar

Zhang, Q., Fan, K., Wang, P., Yu, J., Liu, R., Qi, H., et al. (2016). Carvacrol induces the apoptosis of pulmonary artery smooth muscle cells under hypoxia. Eur. J. Pharmacol. 770, 134–146. doi:10.1016/j.ejphar.2015.11.037

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, C., Ma, C., Yao, H., Zhang, L., Yu, X., Liu, Y., et al. (2018). 12-Lipoxygenase and 12-hydroxyeicosatetraenoic acid regulate hypoxic angiogenesis and survival of pulmonary artery endothelial cells via PI3K/Akt pathway. Am. J. Physiol. Lung Cell. Mol. Physiol. 314, L606–L616. doi:10.1152/ajplung.00049.2017

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, D.-Q., Li, J.-S., Zhang, Y.-M., Gao, F., and Dai, R.-Z. (2018). Astragaloside IV inhibits angiotensin II-stimulated proliferation of rat vascular smooth muscle cells via the regulation of CDK2 activity. Life Sci. 200, 105–109. doi:10.1016/j.lfs.2018.03.036

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, N., Dong, M., Luo, Y., Zhao, F., and Li, Y. (2018). Danshensu prevents hypoxic pulmonary hypertension in rats by inhibiting the proliferation of pulmonary artery smooth muscle cells via TGF-β-smad3-associated pathway. Eur. J. Pharmacol. 820, 1–7. doi:10.1016/j.ejphar.2017.12.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X., Chen, J., Xu, P., and Tian, X. (2018). Protective effects of astragaloside IV against hypoxic pulmonary hypertension. MedChemComm 9, 1715–1721. doi:10.1039/c8md00341f

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, M., Chang, Z., Zhang, P., Jing, Z., Yan, L., Feng, J., et al. (2019a). Protective effects of 18β-glycyrrhetinic acid on pulmonary arterial hypertension via regulation of Rho A/Rho kinsase pathway. Chem. Biol. Interact. 311, 108749. doi:10.1016/j.cbi.2019.108749

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, M., Chang, Z., Zhao, F., Zhang, P., Hao, Y.-J., Yan, L., et al. (2019b). Protective effects of 18β-Glycyrrhetinic acid on monocrotaline-induced pulmonary arterial hypertension in rats. Front. Pharmacol. 10, 13. doi:10.3389/fphar.2019.00013

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Y., Geng, J., Hong, Y., Jiao, L., Li, S., Sun, R., et al. (2019c). Orally administered crocin protects against cerebral Ischemia/reperfusion injury through the metabolic transformation of crocetin by gut microbiota. Front. Pharmacol. 10, 440. doi:10.3389/fphar.2019.00440

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Zhu, M., Zhang, S., Xie, S., Gao, Y., and Wang, Y. (2020). Triptolide attenuates renal damage by limiting inflammatory responses in DOCA-salt hypertension. Int. Immunopharmacol. 89, 107035. doi:10.1016/j.intimp.2020.107035

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, W., Wang, X., Li, J., Xu, M., Ren, X., Liu, H., et al. (2021). Astragaloside IV reduces OxLDL-Induced BNP overexpression by regulating HDAC. J. Healthc. Eng. 2021, 3433615. doi:10.1155/2021/3433615

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, X., Liu, S., Sun, Y., and Li, G. (2022). Tanshinone IIA alleviates monocrotaline-induced pulmonary hypertension in rats through the PI3K/Akt-eNOS signaling pathway. Nan Fang. Yi Ke Da Xue Xue Bao 42 (05.13), 718–723. doi:10.12122/j.issn.1673-4254.2022

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Y., Hernandez, M., Gower, J., Winicki, N., Morataya, X., Alvarez, S., et al. (2022). JAGGED-NOTCH3 signaling in vascular remodeling in pulmonary arterial hypertension. Sci. Transl. Med. 14, eabl5471. doi:10.1126/scitranslmed.abl5471

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Dong, F., Ju, G., Pan, X., Mao, X., and Zhang, X. (2024a). Sodium Houttuyfonate alleviates monocrotaline-induced pulmonary hypertension by regulating Orai1 and Orai2. Am. J. Respir. Cell Mol. Biol. 71, 332–342. doi:10.1165/rcmb.2023-0015OC

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Mao-mao, , Shao, M., and Wang, M. (2024b). Therapeutic potential of natural flavonoids in pulmonary arterial hypertension: a review. Phytomedicine 128, 155535. doi:10.1016/j.phymed.2024.155535

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, L., Wang, G., Li, Z., Yang, J., Li, H., Wang, W., et al. (2024). Molecular pharmacology and therapeutic advances of monoterpene perillyl alcohol. Phytomedicine 132, 155826. doi:10.1016/j.phymed.2024.155826

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, Q., Yaoita, N., Tabuchi, A., Liu, S., Chen, S.-H., Li, Q., et al. (2024). Endothelial heterogeneity in the response to autophagy drives small vessel muscularization in pulmonary hypertension. Circulation 150, 466–487. doi:10.1161/CIRCULATIONAHA.124.068726

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhao, M., Wu, F., Tang, Z., Yang, X., Liu, Y., Wang, F., et al. (2023). Anti-inflammatory and antioxidant activity of ursolic acid: a systematic review and meta-analysis. Front. Pharmacol. 14, 1256946. doi:10.3389/fphar.2023.1256946

PubMed Abstract | CrossRef Full Text | Google Scholar

Zheng, L., Liu, M., Wei, M., Liu, Y., Dong, M., Luo, Y., et al. (2015). Tanshinone IIA attenuates hypoxic pulmonary hypertension via modulating KV currents. Respir. Physiol. Neurobiol. 205, 120–128. doi:10.1016/j.resp.2014.09.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhou, Y., Sun, Y., Li, P., Qin, G., Cheng, Q., Liu, Y., et al. (2018). Monoside antagonizes triptolide-induced hepatocyte apoptosis via the anti-oxidative stress pathway. Nan Fang. Yi Ke Da Xue Xue Bao 38, 949–955. doi:10.3969/j.issn.1673-4254.2018.08.08

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhu, W., Liu, Y., Tang, J., Liu, H., Jing, N., Li, F., et al. (2021). Functional analysis of sterol O-Acyltransferase involved in the biosynthetic pathway of pachymic acid in Wolfiporia cocos. Molecules 27, 143. doi:10.3390/molecules27010143

PubMed Abstract | CrossRef Full Text | Google Scholar

Glossary

Akt Protein kinase B

ARE Antioxidant response element

ASIV Astragaloside IV

Bcl-2 B-cell lymphoma 2

BMP Bone Morphogenetic Protein

BMPR2 Bone morphogenetic protein receptor type II

Bsg Basigin

Ca²⁺ Calcium

CAT Catalase

CCL2 C-C motif chemokine ligand 2

CCN1 Cellular communication network factor 1

CCR2 C-C chemokine receptor 2

CD31 Cluster of differentiation 31

cGAS Cyclic GMP–AMP synthase

CXCL1 C-X-C motif chemokine ligand 1

Cyclins Cell cycle proteins

CyPA Cyclophilin A

Ecs Endothelial cells

eIF2α Eukaryotic translation initiation factor 2-alpha

EndMT Endothelial-to-mesenchymal transition

eNOS Endothelial nitric oxide synthase

ERK Extracellular signal-regulated kinase

ERS Endoplasmic reticulum stress

ET-1 Endothelin-1

GSH Glutathione

GSH-Px Glutathione peroxidase

GSK-3β Glycogen synthase kinase-3β

GSSG Oxidized glutathione

HDAC Histone deacetylase

HIF-1α Hypoxia-inducible factor-1α

HO-1 Heme oxygenase-1

IL-10 Interleukin-10

IL-1β Interleukin-1β

IL-6 Interleukin-6

IL-8 Interleukin-8

iNOS Inducible nitric oxide synthase

K⁺ Potassium

Keap1 Kelch-like ECH-associated protein 1

Kv Voltage-dependent potassium

LDH Lactate dehydrogenase

LPO Lipid peroxides

MAPK Mitogen-activated protein kinase

MCT Monocrotaline

MDA Malondialdehyde

MetAP2 Methionine aminopeptidase-2

miR-204 MicroRNA-204

MMP-2 Matrix metalloproteinase-2

MMP-9 Matrix metalloproteinase-9

Mpap Mean pulmonary arterial pressure

MT Metallothionein

NF-κB Nuclear factor-κB

NO Nitric oxide

Nrf2 Nuclear factor erythroid 2-related factor 2

OXR1 Oxidation resistance 1

p16 Cyclin-dependent kinase inhibitor 2A

p21 Cyclin-dependent kinase inhibitor 1A

PAECs Pulmonary artery endothelial cells

PAH Pulmonary arterial hypertension

p-AKT Phosphorylated AKT

PAP Pulmonary arterial pressure

PARP1 Poly(ADP-ribose) polymerase 1

PASMCs Pulmonary arterial smooth muscle cells

PCNA Proliferating cell nuclear antigen

PDGF Platelet-derived growth factor

PERK Protein kinase RNA-like endoplasmic reticulum kinase

p-GSK-3β Phosphorylated GSK-3β

PI3K Phosphatidylinositol 3-kinase

PPARα Peroxisome proliferator-activated receptor-α

PVR Pulmonary vascular resistance

RhoA Ras homolog family member A

ROCK Rho-associated coiled-coil containing protein kinase

ROS Reactive oxygen species

RV Right ventricular

RVH Right ventricular hypertrophy

RVSP Right ventricular systolic pressure

SIRT1 Silent information regulator 1

Smad2/3 Mothers against decapentaplegic homolog 2/3

SOCE Store-operated calcium entry

SOD Superoxide dismutase

STAT3 Signal transducer and activator of transcription 3

STING Stimulator of interferon genes

SuHx SU5416/hypoxia

TAC Total antioxidant capacity

TGF-β1 Transforming growth factor-β1

TIMP-1 Tissue inhibitor of metal protease 1

TLRs Toll-like receptors

TNF-α Tumor necrosis factor-α

TRPM7 Transient receptor potential melastatin 7

VE-cadherin Vascular endothelial cadherin

VEGF vascular endothelial growth factor

Vwf Von Willebrand factor

α-SMA α-smooth muscle actin

Skp2 S-phase kinase-associated protein 2