Pharmacology activity, toxicity, and clinical trials of Erythrina genus plants (Fabaceae): an evidence-based review

Abstract

The concept of using plants to alleviate diseases is always challenging. In West Java, Indonesia, a local plant, named dadap serep has been traditionally used to reduce blood glucose, fever, and edema, by pounding the leaves and applying them on the inflamed skin, or boiled and consumed as herbal tea. This plant belongs to the Erythrina genus, which covers approximately 120 species. The scope of this review (1943–2023) is related to the Global Development Goals, in particular Goal 3: Good Health and Wellbeing, by focusing on the pharmacology activity, toxicity, and clinical trials of Erythrina genus plants and their metabolites, e.g., pterocarpans, alkaloids, and flavonoids. Articles were searched on PubMed and ScienceDirect databases, using “Erythrina” AND “pharmacology activity” keywords, and only original articles written in English and open access were included. In vitro and in vivo studies reveal promising results, particularly for antibacterial and anticancer activities. The toxicity and clinical studies of Erythrina genus plants are limitedly reported. Considering that extensive caution should be taken when prescribing botanical drugs for patients parallelly taking a narrow therapeutic window drug, it is confirmed that no interactions of the Erythrina genus were recorded, indicating the safety of the studied plants. We, therefore, concluded that Erythrina genus plants are promising to be further explored for their effects in various signaling pathways as future plant-based drug candidates.

1 Introduction

Discovering herbal-based drugs is always challenging. Plants’ metabolites, e.g., flavonoids and polyphenols, have been reported for their role in representing pharmacological activities (González et al., 2011; Rosdianto et al., 2020; Stromsnes et al., 2021).

In West Java, Indonesia, a local plant, named dadap serep, has been traditionally used to reduce blood glucose, fever, and edema. The leaves are usually pounded and applied to the inflamed skin, or boiled and consumed as herbal tea. In order to understand the reason this plant exhibits the ability to cure diseases, we search for scientific information related to the plant. Dadap serep, botanical name Erythrina subumbrans (Hassk.) Merr.) belongs to the Erythrina genus of the family Fabaceae. The Erythrina genus covers approximately 120 species worldwide. Erythrina subumbrans (Hassk.) Merr.) (Fabaceae) trees are large, up to 22 m tall. The leaves are 3-pinnated, with leaf blades almost round to rhombic shape, rounded base, larger tip, with a flat edge. These plants are widely grown in the Southeast Asia region (http://ipbiotics.apps.cs.ipb.ac.id/index.php/tumbuhanObat/297). The native range of this species is from China (Yunnan) to Tropical Asia and Southwest Pacific (https://powo.science.kew.org/taxon/urn:lsid:ipni.org:names:494601-1#source-KBD).

This article aims to review the pharmacology activities, in silico studies, toxicity studies in animal models, and clinical trials of the Erythrina genus plants, to ensure the safety of their administration to humans.

2 Radical scavenging activity of the phytochemicals

The Erythrina genus of the family Fabaceae includes trees, shrubs, and herbaceous plants with orange to bright red flowers, rich in pterocarpans and alkaloids (Rukachaisirikul et al., 2007a; Phukhatmuen et al., 2021), flavonoids (Nyandoro et al., 2017; Deviani et al., 2022; Simão et al., 2022), triterpenes, steroids, alkyl trans-ferulates, proteins, saponins, and lecithin (Kumar et al., 2010), gallic and caffeic acids (Muthukrishnan et al., 2016). Pterocarpans comprise a large group of isoflavonoids and function as phytoalexins (plant antimicrobial mechanism) and are mostly found in the Leguminosae (Fabaceae) family (Jiménez-González et al., 2011). Flavonoids are low-molecular-weight polyphenolic metabolites in plants that are further classified into subgroups, e.g., flavones, flavonols, isoflavones, chalcones, and anthocyanins (Panche et al., 2016). Pterocarpans, flavonoids, and alkaloids are considered responsible for Erythrina’s pharmacology activities.

The radical scavenging activity of Erythrina genus plants has been verified by employing various methods, such as ferrous reducing antioxidant capacity (FRAC) (Afzal et al., 2022), 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical (Dzoyem et al., 2014; Deviani et al., 2022; Fofana et al., 2022), and 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulphonic acid) diamonium salt (ABTS) (Dzoyem et al., 2014).

The ethyl acetate fraction and lupinifolin, a flavanone isolated from E. crista-galli L. twigs collected in Cihideung, West Java, Indonesia, have confirmed its capability to scavenge 50% of the initial DPPH radicals with a value of 64.41 and 128.64 μg/mL, respectively, better than the other flavanones, e.g., citflavanone and lonchocarpol A. It was explained that the prenyl and the pyran in lupinifolin contribute to this capability (Deviani et al., 2022). Silver nanoparticles (Ag-NPs) synthesized from the leaf and bark extracts of E. suberosa Roxb. exhibited significant reducing activity towards ferric chloride solution (Afzal et al., 2022). The radical scavenging activity of E. caffra Thunb. (leaves) (Dzoyem et al., 2014) and E. senegalensis DC. (stem bark) (Fofana et al., 2022) were also delineated. Moreover, a previous in silico approach disclosed that the radical scavenging activity of Erythrina’s flavanone, namely, mildbone and mildbenone, is predominantly associated with the second bond dissociation enthalpy of a second hydrogen atom transfer (Anouar, 2016). Mildbone and mildbenone, polar metabolites in Erythrina, were suggested to contribute to the various biological activities of Erythrina plants (Jiménez-Cabrera et al., 2020).

3 Pharmacology activities

Most of the studies described Africa and Brazil as the origin locations of Erythrina plants (Fabaceae). The scope of articles was those published from 1943 to 2023 (depicted in Figure 1).

FIGURE 1

The most studied activities were antibacterial and anticancer, although a few works reported anti-inflammatory, antidiabetic, estrogenic, antifungal, antidepressant, and other activities. The stem bark was the most explored and considered an active part of the Erythrina genus plants, followed by the leaves, twigs, root bark, and seeds. The pharmacology activities of the Erythrina genus plants are summarized in Supplementary Table S1.

3.1 Antibacterial activity

Antibacterial activity was confirmed to belong to E. subumbrans (Hassk.) Merr. (twigs and roots) (Phukhatmuen et al., 2021), E. verna Vell. (stem bark) (Simão et al., 2022), E. suberosa Roxb. (leaves and bark) (Afzal et al., 2022), E. lysistemon Hutch., Kew Bull. (stem bark) (Sadgrove et al., 2020), E. poeppigiana (Walpers) O.F. Cook (leaves) (Dzoyem et al., 2014). A notable antibacterial activity of plant extracts is an auspicious result since extracts contain a mixture of metabolites (Dzoyem et al., 2014). It was described previously that the prenylation of flavonoids increases the ability to penetrate the membrane cell of bacteria by building a strong lipophilic arm to the molecule. An OH group attached to the same aromatic ring as the prenyl strengthens the antibacterial activity (Sadgrove et al., 2020). Alkaloids, a group of nitrogen-containing organic compounds, were reported for their cell membrane-damaging mechanism. Alkaloids could interfere with the energy metabolisms thus inhibiting bacterial growth (Djeussi et al., 2015; Sadgrove et al., 2020; Alencar de Barros et al., 2021).

Antibacterial mechanisms of plant metabolites may include, but are not restricted to, the inhibition of bacterial cell wall synthesis, alteration of the permeability of the cell membrane permeability, and/or blocking of the bacterial synthesis of protein. Implying this, Erythrina plants, that contain flavonoids and alkaloids, may have the potential to kill Gram-positive and Gram-negative bacteria (Dzoyem et al., 2014; Djeussi et al., 2015; Sadgrove et al., 2020; Alencar de Barros et al., 2021; Phukhatmuen et al., 2021; Afzal et al., 2022; Simão et al., 2022; Yenesew et al., 2005).

3.2 Anticancer activity

The anticancer activity of the Erythrina genus plants has also been validated and reported in 7 articles against different cancer cell lines. The ethyl acetate subfraction of E. senegalensis DC. stem bark exhibited anticancer activity against U373, MCF-7, A549, SKMEL-28, and B16F10 cells, despite its lower phenolic and flavonoid content (Fofana et al., 2022). Flavanones isolated from the leaves of E. crista galli L. were evaluated using the Arabidopsis thaliana pER8: GUS reporter assay while their molecular interactions with the residues Arg394, Glu353, and His524 in the active site of human estrogen receptor R (ERR) were studied, thus revealing their anticancer activity (Ashmawy et al., 2016). The essential oils contained in the leaves of E. variegata Linn. blocked the proliferation of breast cancer (MDA-MB-231 and MCF-7) cells and non-cancerous mammary epithelial cells (HMLE) (Xing et al., 2019). Another in vitro study of E. suberosa Roxb. Stem bark described that two isolated metabolites, namely, 4′-methoxy licoflavanone, and alpinumisoflavone, inhibited HL-60 cell proliferation and induced apoptosis (Kumar et al., 2013). Alpinumisoflavone isolated from the stem barks of E. lysistemon reduced the viability and induced the apoptosis of human lung cancer cell lines H2108 and H1299 (Namkoong et al., 2011). Prenylated pterocarpans isolated from the stem bark of E. addisoniae Hutch. & Dalziel revealed weak to moderate toxicity towards H4IIE hepatoma cells and decreased activation of the ERK kinase (p44/p42) (Wätjen et al., 2007). Xanthoxyletin isolated from the aerial part of E. variegata L. induced apoptosis and cell cycle arrest in human gastric adenocarcinoma SGC-7901 cells (Rasul et al., 2011).

Taken together, apoptosis in various cancer cells may be considered the main mechanism of Erythrina metabolites. Apoptosis, identified by cell shrinkage and DNA fragmentation, is structured by a series of molecular reactions that could be stimulated extrinsically or intrinsically. Apoptosis is activated by caspases (cysteine-aspartic proteases) as effectors of the process (Hail et al., 2006). The intrinsic pathway of apoptosis is initiated when internal cellular stress occurs due to DNA damage or endoplasmic reticulum stress, which eventually activates the BCL-2 homology 3 protein. The extrinsic pathway is activated when death receptors (DR1-DR8) are induced by receptor binding or aggregation (Cavalcante et al., 2019).

3.3 Antidiabetic activity

Metabolites isolated from the twigs and roots of E. subumbrans (Hassk.) Merr. were confirmed to inhibit α-glucosidase activity and/or α-amylase activity (Phukhatmuen et al., 2021). Prenylated flavonoids isolated from the root bark of E. mildbraedii Harms inhibited PTP1B activity with IC₅₀ values ranging from 5.3 to 42.6 mM as reported by Jang and co-workers in Korea. The assay was carried out using a human recombinant PTP1B kit. There is very little information regarding the pharmacology activity and mechanism, and no discussion has been provided since this work was presented as Notes (Jang et al., 2008). PTP1B, a tyrosine phosphatase protein, plays important contributions in intracellular signal transduction by regulating the cellular level of tyrosine phosphorylation. It downregulates insulin signaling by dephosphorylating the insulin receptor (IR) and insulin receptor substrate (IRS), thus dysfunction of this protein may lead to numerous ailments such as cancer, diabetes, and obesity (Sun et al., 2012).

An alteration in insulin signaling, predominantly in the IRS/phosphoinositide-3-kinase (PI-3K)/protein kinase B (PKB) axis, stimulates the development of insulin resistance. Insulin resistance is generally associated with obesity, which is a risk factor for type 2 diabetes mellitus (T2DM) (Wondmkun, 2020). Mature insulin is stored in granules until it is needed to be released when blood glucose levels are elevated, e.g., following a high carbohydrate intake. Several factors may also activate insulin release, e.g., amino acids, fatty acids, and hormones (Boland et al., 2017). The occurrence of insulin resistance in T2DM patients may also be caused by an abnormal synthesis of insulin, a mutation of insulin receptors, or the presence of an insulin antagonist (Al-Ishaq et al., 2019).

Interestingly, flavonoids are thought to play an important role in regulating carbohydrate hydrolysis, as well as insulin signaling and secretion (Al-Ishaq et al., 2019). It was announced that dietary intake of anthocyanins and anthocyanin-rich fruit (blueberries) was correlated with a lower risk of T2DM in both males and females (Wedick et al., 2012). A reduction in IL-6 and TNF-α was observed following the intake of different berries, suggesting an important role of these fruits in modulating the lipid profile and inflammatory cytokines in subjects with metabolic diseases (Venturi et al., 2023).

3.4 Anti-inflammatory activity

The anti-inflammatory activity of Erythrina plants was also reported, although limited. We found 4 articles that described the anti-inflammatory activity by various mechanisms as follows:

The fractions obtained from the dichloromethane stem bark extract of E. verna Vell have confirmed their inhibitory activity on nitric oxide (NO) production and blocked TNF-α activity. This in vitro study was performed on a murine RAW 264.7 macrophage cell line and the quantification of NO and TNF-α was done using a commercially enzyme-linked immunosorbent assay kit. In their study, Simão and others employed a bioassay-guided procedure, which resulted in two active flavonoid metabolites, namely, alpinumisoflavone and erythratidinone (Simão et al., 2022).

Previously, Machado and his co-workers studied the purification, biochemical characterization, and anti-inflammatory evaluation of a novel Kunitz trypsin inhibitor from E. velutina Willd. Seeds. The metabolites were purified by NH₄(SO₄)₂, fractionated, and eventually underwent trypsin-sepharose affinity chromatography and an RP-HPLC. It was confirmed that the metabolites isolated from the seeds of E. velutina Willd. Strongly inhibited trypsin by a non-competitive mechanism, reduced leukocyte migration, decreased TNF-α release, and stimulated IFN-α and IL-12 production, thus indicating a promising anti-inflammatory activity (Machado et al., 2013).

The leaves and bark extract of E. abyssinica Lam. ex DC. ointments exhibited low anti-inflammatory and wound-healing properties. It was reported by Marume and the research team that wounds of animals treated with the extract ointments revealed almost similar recovery, although not significantly different, to those of animals treated with 3% oxytetracycline ointment (Marume et al., 2017).

The ethanol extract of E. senegalensis DC. leaves were assayed in vivo using egg albumin-induced paw edema in the rat model and resulted in a strong activity in stabilizing the erythrocyte membrane, and significantly decreased albumin denaturation, platelet aggregation, phospholipase A2 and protease activity (Enechi et al., 2021). Alkaloids isolated from the bark of Erythrina crista-galli L., purchased in September 2004 in São Paulo, Brazil, inhibit the production of nitric oxide in RAW264.7 cells (Ozawa et al., 2010). There are numerous complex mechanisms and signaling pathways related to inflammation, thus these reports may not depict the whole picture of how the botanical drugs suppress the inflammatory process. Moreover, it should be noted that different assay methods may notably affect the results.

3.5 Other pharmacology activities

Erythrina plants have also been explored for other activities, e.g., estrogenic activity by increasing uterus and vaginal index and keratinizing vaginal cells, inducing uterine and vaginal hypertrophy associated with endometrial proliferation (Li et al., 2019), antiviral against respiratory syncytial virus (RSV) and herpes simplex virus (HSV-2) (Mollel et al., 2022), strong antifungal activities against Candida albicans and C. glabrata strains and clinical isolates (Harley et al., 2022), Leishmanicidal activity against the promastigote forms of L. amazonensis (Callejon et al., 2014), anxiolytic and anti-depressant (Chu et al., 2019), bone protective effect in the tibia of ovariectomized rats (Xiao et al., 2021), antihepatotoxicity by reducing the levels of transaminases, ALP, bilirubin, and LDH to normal (Mujahid et al., 2017), retention of fear memory but did not prevent the extinction of fear memory (de Oliveira et al., 2014), Aurora kinase inhibitor (Hoang et al., 2016), antiplasmodial (Rukachaisirikul et al., 2007b; Waiganjo et al., 2020), inhibitor of neuronal nicotinic receptors (Setti-Perdigão et al., 2013).

To obtain the total active metabolites that contribute to the pharmacology activities of Erythrina genus plants, we further tabulated these metabolites and their studies on different pharmacological assays in Supplementary Table S2.

4 In silico study

Regrettably, phenolic metabolites of the Erythrina genus plants have been very limitedly studied for their interaction with various proteins. However, the limited studies are described below.

Phenolic metabolites of Erythrina × neillii (a cross-hybrid between E. herbacea L. and E. humeana Spreng), were reported for their interaction with Arg136, Met34, and Gly139 of heme oxygenase-1 (HO-1), a macromolecule that plays a role in cellular protection and oxidative catabolism of heme. Stimulation of HO-1 may reduce cardiovascular disease (Gabr et al., 2019). Phaseollin of E. variegata L. built interaction with significant fitness score and hydrogen bonds with Tyr354 and Ser499 residues in both COX-1 and COX-2, which is considered a potent analgesic candidate (Uddin et al., 2014). Tyr354 is one of the key residues constituting the active site of human COX-1, along with Arg119, Tyr384, Ile433, His512, Phe517, and Ile522 (Dhanjal et al., 2015). Polyphenolic metabolites isolated from E. crista-galli L. could interact with Arg394, Glu353, and His524 residues of the human estrogen receptor R (ERR), thus revealing a promising phytoestrogenic activity (Ashmawy et al., 2016). Moreover, diprenylgenistein and phaseollin isolated from the twigs of E. crista-galli L. showed the highest binding affinity towards CDK2 protein, revealing its anticancer activity (Imanuddin et al., 2023). Cyclin-dependent kinases (CDKs) are proteins that regulate the transition of cell cycle phases. Cyclin E binds and activates CDK2 to promote S-phase entry and progression. Cyclin E/CDK2 complex eventually phosphorylates various substrates to control essential cellular processes (Fagundes and Teixeira, 2021).

There is no report on the in silico study of pterocarpans of the Erythrina genus plants, thus unlatching the chance to be further investigated. However, a few articles reported in silico studies of pterocarpans from other plants.

One article reported that pterocarpans isolated from Desmodium gangeticum could interact with tyrosine phosphate kinase similarly to the protein’s inhibitors (Meena et al., 2022). Protein kinases are responsible for the phosphorylation process to activate the function of other proteins. Inhibitors of kinases interact in different modes depending on the specific binding sites and conformational aspects of the enzyme, which are determined by two conditions, e.g., (1) the Asp-Phe-Gly (DFG) motif, as part of the activation loop, and (2) the αC-helix. Most kinase inhibitors interact in the active form (conformational state: DFG-in, αC-helix-in), and are classified as type I inhibitors. Type II inhibitors attach to the inactive state (conformational state: DFG-out, αC-helix-out) (Abdelbaky et al., 2021). It is interesting to explore the binding modes of pterocarpans to kinases and whether these compounds are categorized as type I or type II inhibitors.

Pterocarpans isolated from Indigofera aspalathoides were reported could interact with Ser530 and Tyr385 in COX-1 and COX-2 binding pockets. The interaction with Ser530 is believed to be important in inhibiting the catalytic process of these enzymes (Selvam et al., 2004). In the biosynthesis of prostaglandin H2 (PGH2), the substrate of COX, namely, arachidonic acid, has to enter the cyclooxygenase narrow channel with its carboxylate group attaches (by building hydrogen bonds) to Arg120 and Tyr355, two residues located at the channel opening, and its ω-end occupies in a hydrophobic cavity at upwards position of Ser530 (Malkowski et al., 2000; Vecchio et al., 2010). It has been confirmed that acetylation of Ser530 by acetylsalicylic acid could inhibit the synthesis of prostaglandins (Giménez-Bastida et al., 2019).

Another in silico study confirmed that pterocarpans contained in Sophora flavescens interact with neuraminidase by occupying a binding pocket adjacent to the active site. The methanol extract of this plant at 30 ppm reduced neuraminidase activity by 90% (Ryu et al., 2008).

5 Toxicity studies

In fact, there are only very limited toxicity studies on Erythrina genus plants.

An acute toxicity study of E. senegalensis DC. stem extract in mice (Mus musculus) with doses of 1,250 to 12,500 mg/kg body weight (BW) did not induce mortality or significant behavioral changes. In a sub-chronic toxicity study in rats (Rattus norvegicus), daily oral administration of E. senegalensis DC. stem extract at the dose of 600 mg/kg BW resulted in a significant elevation in the relative BW but no significant alterations in the hematological parameters, suggesting its safety (Atsamo et al., 2011).

Chronic oral toxicity studies of E. mulungu Mart. ex Benth. Mart. ex Benth. (synonym = E. verna Vell. or Corallodendron mulungu (Mart. ex Benth.) Kuntze or E. flammea Herzog) stem bark extract in mice (Mus musculus) at a dose of 1,000 mg/kg BW resulted in alterations of biochemical parameters of the liver and cardiovascular functions. Hematological analysis indicated significant decreases in the red blood cells. Oral daily doses of 500 and 1,000 mg BW of E. mulungu Mart. ex Benth. Stem bark extract increased the relative weights of the liver and heart and serum malondialdehyde levels. Significant histopathological changes in myocardial and degeneration of hepatocytes also occurred (Adeneye, 2014).

A sub-chronic toxicity study of the methanol extract of E. variegata Linn. leaves on male Wistar rats (Rattus norvegicus) revealed slight changes in hematological parameters but were within the normal range, except for BUN and SGPT. Histopathological examination indicated increased damage to the liver and kidney cells, however, doses of 250, 500, and 1,000 mg/kg BW did not cause toxicity in animal models (Herlina et al., 2017). Table 1 tabulates the toxicity studies of the Erythrina plants.

The toxicity of the metabolites contained in the Erythrina genus plants was not commonly reported. However, an article written by Unna and Greslin explained that erythroidine, an alkaloid isolated from Erythrina americana Mill., and other alkaloids, namely, 9-erythroidine, erythramine, erythraline, and erythratine revealed a curarizing effect similarly to that of the crude seed extracts (Unna and Greslin, 1943). It was pointed out that the curarizing effect of a drug changes the electrical activity of the cerebral cortex chiefly due to hypoxia and hypotension (Skorobogatov, 1967). The other major metabolites such as flavonoids and pterocarpans have been proven as safe.

6 Clinical study

There are very limited studies on the efficacy and safety of the Erythrina genus plants in humans. We found only 2 articles, both using E. mulungu Mart. ex Benth. (synonym = E. verna Vell. or Corallodendron mulungu (Mart. ex Benth.) Kuntze or E. flammea Herzog) as an antianxiety in patients who underwent dental surgery.

Study 1. A randomized, triple-blind, clinical control trial was performed on 200 patients who underwent oral surgery of their third mandibular molars (consort number NCT02065843). The patients were treated with either Passiflora incarnata (500 mg), E. mulungu Mart. ex Benth. (500 mg), or midazolam (15 mg) orally 60 min prior to the surgery. The anxiety level of the patients was analyzed using questionnaires and measurements of heart rate, blood pressure, and oxygen saturation (SpO2). It was reported that P. incarnata revealed a similar effect to midazolam but differed from placebo and E. mulungu Mart. ex Benth., indicating that E. mulungu could not be used to reduce the anxiety of the patients (da Cunha et al., 2021).

Study 2. A similar randomized, double-blind, crossover study was performed on 30 healthy adult patients who underwent bilateral surgery of asymptomatic, impacted mandibular third molars (consort number NCT01948622). The patients were treated with either E. mulungu Mart. ex Benth. (500 mg) or a placebo (500 mg) orally 60 min before the surgery. To avoid pain and swelling after surgery, the patients were given a single dose of intra-muscular dexamethasone and an antiseptic mouthwash containing chlorhexidine gluconate 30 min before surgery. The level of anxiety was analyzed using questionnaires and measurements of blood pressure, heart rate, and oxygen saturation. It was reported that E. mulungu Mart. ex Benth. had shown an anxiolytic effect without significant changes in physiological parameters (Silveira-Souto et al., 2014).

7 Botanical drug-drug interaction

Extensive caution should be considered when prescribing botanical drugs for patients parallelly taking a narrow therapeutic window drug. The botanical drugs may dangerously alter the main drug or cause ineffectiveness. Taking this into consideration, we studied the Herb-Drug Interaction Chart (Mills and Bone, 2005; ESCOP, 2023; Standard Process, 2023) and found that no interactions of the Erythrina genus were recorded, indicating the safety of the studied plants.

8 Conclusion

There are 16 of the 120 species of the Erythrina genus plants with confirmed pharmacological activities. Antibacterial and anticancer were the most studied activities, although a few works reported anti-inflammatory, antidiabetic, estrogenic, antifungal, antidepressant, and other activities. The extracts of the Erythrina genus have revealed anticancer activity against human glioblastoma astrocytoma (U-373), human breast cancer cell line with estrogen, progesterone, and glucocorticoid receptors (MCF-7), human epithelial breast cancer (MDA-MB-231), human melanoma (SKMEL-28), murine melanoma (B16F10), human promyelocytic leukemia (HL-60), lung cancer (H2108, H1299, H411E), human adenocarcinoma alveolar basal epithelial (A549), and human gastric cancer (SGC-7901) cells. Studies of the effect of these plant extracts on non-cancerous cells are limited, nevertheless, a study reported that the Erythrina plant extract did not show cytotoxicity on HMLE (immortalized human mammary epithelial), a non-cancerous cell.

The stem bark was the most explored and considered the main active part of the Erythrina genus plants. Sixty-three metabolites have been isolated from various parts of the plants, comprised of pterocarpans, flavonoids, alkaloids, triterpenoids, glycosides, steroids, chromenes, coumarins, and carboxylic acids. The most abundant classes are pterocarpans and flavonoids.

There are very limited toxicity studies on Erythrina genus plants, among those are E. senegalensis DC., E. mulungu Mart. ex Benth. (synonym = E. verna Vell. or Corallodendron mulungu (Mart. ex Benth.) Kuntze or E. flammea Herzog), and E. variegata Linn. All these studies indicated the safety of the higher doses of the plant extracts in animal models. The toxicity of the metabolites contained in the Erythrina genus plants was not commonly reported. However, alkaloids isolated from E. americana Mill. namely, erythroidine, 9-erythroidine, erythramine, erythraline, and erythratine were reported for their curare-like effect on frogs.

There are very limited human studies on Erythrina genus plants. Only one species, E. mulungu Mart. ex Benth. has been reported as a weak anxiolytic in dental surgery in randomized, controlled clinical trials. It should be noted that the selected articles have employed different experimental designs.

Most of the pharmacological studies were carried out on plant extracts, not as nutraceuticals or supplements, or pure metabolites, and almost all studies reported significant statistical analysis results. Not all articles described their procedures in detail, thus affecting the reliability of the studies and limiting our interpretations. Nonetheless, we feel optimistic that the Erythrina genus plants are promising to be further explored for their effects in various signaling pathways as future plant-based drug candidates. We are certain this review has unraveled comprehensive perspectives of Erythrina genus plants thus providing beneficial insights into plant-based drug discovery.

References

• 1

  AbdelbakyI.TayaraH.ChongK. T. (2021). Prediction of kinase inhibitors binding modes with machine learning and reduced descriptor sets. Sci. Rep.11 (1), 706. 10.1038/s41598-020-80758-4

  • CrossRef
  • Google Scholar

• 2

  AdeneyeA. A. (2014). Subchronic and chronic toxicities of african medicinal plants. Toxicol. Surv. Afr. Med. Plants102, 99–133. 10.1016/B978-0-12-800018-2.00006-6

  • CrossRef
  • Google Scholar

• 3

  AfzalS.QurashiA. W.SarfrazB.LiaqatI.SadiqaA.MuhtaqM.et al (2022). A comparative analysis of antimicrobial, antibiofilm and antioxidant activity of silver nanoparticles synthesized from Erythrina suberosa Roxb. and Ceiba pentandra. J. Oleo Sci.71 (4), 523–533. 10.5650/jos.ess21347

  • CrossRef
  • Google Scholar

• 4

  Alencar de BarrosK. M.SardiJ. C. O.Maria-NetoS.MacedoA. J.RamalhoS. R.Lourenço de OliveiraD. G.et al (2021). A new Kunitz trypsin inhibitor from Erythrina poeppigiana exhibits antimicrobial and antibiofilm properties against bacteria. Biomed. Pharmacother.144, 112198. 10.1016/j.biopha.2021.112198

  • CrossRef
  • Google Scholar

• 5

  Al-IshaqR. K.AbotalebM.KubatkaP.KajoK.BüsselbergD. (2019). Flavonoids and their anti-diabetic effects: cellular mechanisms and effects to improve blood sugar levels. Biomolecules9 (9), 430. 10.3390/biom9090430

  • CrossRef
  • Google Scholar

• 6

  AnouarE. H. (2016). Antioxidant activity of mildbone and mildbenone secondary metabolites of Erythrina mildbraedii Harms: a theoretical approach. Comput. Theor. Chem.1077, 106–112. 10.1016/j.comptc.2015.11.003

  • CrossRef
  • Google Scholar

• 7

  AshmawyN. S.AshourM. L.WinkM.El-ShazlyM.ChangF. R.SwilamN.et al (2016). Polyphenols from Erythrina crista-galli: structures, molecular docking and phytoestrogenic activity. Molecules21 (6), 726. 10.3390/molecules21060726

  • CrossRef
  • Google Scholar

• 8

  AtsamoA. D.NguelefackT. B.DattéJ. Y.KamanyiA. (2011). Acute and subchronic oral toxicity assessment of the aqueous extract from the stem bark of Erythrina senegalensis DC (Fabaceae) in rodents. J. Ethnopharmacol.134 (3), 697–702. 10.1016/j.jep.2011.01.023

  • CrossRef
  • Google Scholar

• 9

  BolandB. B.RhodesC. J.GrimsbyJ. S. (2017). The dynamic plasticity of insulin production in β-cells. Mol. Metab.6 (9), 958–973. 10.1016/j.molmet.2017.04.010

  • CrossRef
  • Google Scholar

• 10

  CallejonD. R.RiulT. B.FeitosaL. G.GuaratiniT.SilvaD. B.AdhikariA.et al (2014). Leishmanicidal evaluation of tetrahydroprotoberberine and spirocyclic erythrina-alkaloids. Molecules19 (5), 5692–5703. 10.3390/molecules19055692

  • CrossRef
  • Google Scholar

• 11

  CavalcanteG. C.SchaanA. P.CabralG. F.Santana-da-SilvaM. N.PintoP.VidalA. F.et al (2019). A cell's fate: an overview of the molecular biology and genetics of apoptosis. Int. J. Mol. Sci.20 (17), 4133. 10.3390/ijms20174133

  • CrossRef
  • Google Scholar

• 12

  ChuH. B.TanY. D.LiY. J.ChengB. B.RaoB. Q.ZhouL. S. (2019). Anxiolytic and anti-depressant effects of hydroalcoholic extract from Erythrina variegata and its possible mechanism of action. Afr. Health Sci.19 (3), 2526–2536. 10.4314/ahs.v19i3.28

  • CrossRef
  • Google Scholar

• 13

  da CunhaR. S.AmorimK. S.GercinaA. C.de OliveiraA. C. A.Dos Santos MenezesL.GroppoF. C.et al (2021). Herbal medicines as anxiolytics prior to third molar surgical extraction. A randomized controlled clinical trial. Clin. Oral Investig.25 (3), 1579–1586. 10.1007/s00784-020-03468-1

  • CrossRef
  • Google Scholar

• 14

  de OliveiraD. R.ZamberlamC. R.GaiardoR. B.RêgoG. M.CeruttiJ. M.CavalheiroA. J.et al (2014). Flavones from Erythrina falcata are modulators of fear memory. BMC Complement. Altern. Med.14, 288. 10.1186/1472-6882-14-288

  • CrossRef
  • Google Scholar

• 15

  DevianiV.HardiantoA.FarabiK.HerlinaT. (2022). Flavanones from Erythrina crista-galli twigs and their antioxidant properties determined through in silico and in vitro studies. Molecules27 (18), 6018. 10.3390/molecules27186018

  • CrossRef
  • Google Scholar

• 16

  DhanjalJ. K.SreenidhiA. K.BafnaK.KatiyarS. P.GoyalS.GroverA.et al (2015). Computational structure-based de novo design of hypothetical inhibitors against the anti-inflammatory target COX-2. PLoS ONE10 (8), e0134691. 10.1371/journal.pone.0134691

  • CrossRef
  • Google Scholar

• 17

  DjeussiD. E.SandjoL. P.NoumedemJ. A.OmosaL. K.T NgadjuiB.KueteV. (2015). Antibacterial activities of the methanol extracts and compounds from Erythrina sigmoidea against Gram-negative multi-drug resistant phenotypes. BMC Complement. Altern. Med.15, 453. 10.1186/s12906-015-0978-8

  • CrossRef
  • Google Scholar

• 18

  DzoyemJ. P.McGawL. J.EloffJ. N. (2014). In vitro antibacterial, antioxidant and cytotoxic activity of acetone leaf extracts of nine under-investigated Fabaceae tree species leads to potentially useful extracts in animal health and productivity. BMC Complement. Altern. Med.14, 147. 10.1186/1472-6882-14-147

  • CrossRef
  • Google Scholar

• 19

  EnechiC. O.OkekeE. S.IsioguguN. O.EzeakoC. E.NathanielF. O.OlisaA.et al (2021). Phytochemical composition and anti-inflammatory potential of flavonoid-rich fraction of Erythrina senegalensis DC (Fabaceae) leaf. Heliyon. Available at: http://dx.doi.org/10.2139/ssrn.3996877.

  • Google Scholar

• 20

  ESCOP (2023). Table of herb-drug interactions based on the monographs of ESCOP. Available at: https://escop.com/interactions/ (Accessed on September 30, 2023).

  • Google Scholar

• 21

  FagundesR.TeixeiraT. L. K. (2021). Cyclin E/CDK2: DNA Replication, replication stress and genomic instability. Front. Cell Dev. Biol.9. 10.3389/fcell.2021.774845

  • CrossRef
  • Google Scholar

• 22

  FofanaS.DelporteC.Calvo EspositoR.OuédraogoM.Van AntwerpenP.GuissouI. P.et al (2022). In vitro antioxidant and anticancer properties of various E. senegalensis extracts. Molecules27 (8), 2583. 10.3390/molecules27082583

  • CrossRef
  • Google Scholar

• 23

  GabrS. K.BakrR. O.MostafaE. S.El-FishawyA. M.El-AlfyT. S. (2019). Antioxidant activity and molecular docking study of Erythrina × neillii polyphenolics. S Afr. J. Bot.121, 470–477. 10.1016/j.sajb.2018.12.011

  • CrossRef
  • Google Scholar

• 24

  Giménez-BastidaJ. A.BoeglinW. E.BoutaudO.MalkowskiM. G.SchneiderC. (2019). Residual cyclooxygenase activity of aspirin-acetylated COX-2 forms 15 R-prostaglandins that inhibit platelet aggregation. FASEB J.33 (1), 1033–1041. 10.1096/fj.201801018R

  • CrossRef
  • Google Scholar

• 25

  GonzálezR.BallesterI.López-PosadasR.SuárezM. D.ZarzueloA.Martínez-AugustinO.et al (2011). Effects of flavonoids and other polyphenols on inflammation. Crit. Rev. Food Sci. Nutr.51 (4), 331–362. 10.1080/10408390903584094

  • CrossRef
  • Google Scholar

• 26

  HailN.JrCarterB. Z.KonoplevaM.AndreeffM. (2006). Apoptosis effector mechanisms: a requiem performed in different keys. Apoptosis11 (6), 889–904. 10.1007/s10495-006-6712-8

  • CrossRef
  • Google Scholar

• 27

  HarleyB. K.QuagraineA. M.NegloD.AggreyM. O.OrmanE.Mireku-GyimahN. A.et al (2022). Metabolite profiling, antifungal, biofilm formation prevention and disruption of mature biofilm activities of Erythrina senegalensis stem bark extract against Candida albicans and Candida glabrata. PLoS One17 (11), e0278096. 10.1371/journal.pone.0278096

  • CrossRef
  • Google Scholar

• 28

  HerlinaT.MadihahM.DeniD.AmienS. (2017). Subchronic toxicity of methanol extract from Erythrina variegata (Leguminosae) leaves on male Wistar rats (Rattus norvegicus). Molekul12 (1), 88. 10.20884/1.jm.2017.12.1.349

  • CrossRef
  • Google Scholar

• 29

  HoangN. T.PhuongT. T.NguyenT. T.TranY. T.NguyenA. T.NguyenT. L.et al (2016). In vitro characterization of derrone as an aurora kinase inhibitor. Biol. Pharm. Bull.39 (6), 935–945. 10.1248/bpb.b15-00835

  • CrossRef
  • Google Scholar

• 30

  ImanuddinA. N. J.WianiI.HardiantoA.HerlinaT. (2023). Flavonoids from extract butanol of twigs Erythrina crista-galli against the breast cancer cell line within in silico method. Trends Sci.20 (7), 5350. 10.48048/tis.2023.5350

  • CrossRef
  • Google Scholar

• 31

  JangJ.NaM.ThuongP. T.NjamenD.MbaforJ. T.FomumZ. T.et al (2008). Prenylated flavonoids with PTP1B inhibitory activity from the root bark of Erythrina mildbraedii. Chem. Pharm. Bull. (Tokyo)56 (1), 85–88. 10.1248/cpb.56.85

  • CrossRef
  • Google Scholar

• 32

  Jiménez-CabreraT.BautistaM.Velázquez-GonzálezC.Jaramillo-MoralesO. A.Guerrero-SolanoJ. A.Urrutia-HernándezT. A.et al (2020). Promising antioxidant activity of Erythrina genus: an alternative treatment for inflammatory pain?Int. J. Mol. Sci.22 (1), 248. 10.3390/ijms22010248

  • CrossRef
  • Google Scholar

• 33

  Jiménez-GonzálezL.Hernández-CervantesC.Álvarez-CorralM.Muñoz-DoradoM.Rodríguez-GarcíaI. (2011). Synthesis of pterocarpans. Nat. Prod. Comm.6 (4), 1934578X1100600–554. 10.1177/1934578x1100600414

  • CrossRef
  • Google Scholar

• 34

  JumaB. F.MajindaR. R. T. (2005). Constituents of Erythrina lysistemon: their brine shrimp lethality, antimicrobial and radical scavenging activities. Nat. Prod. Comm.1 (2), 1934578X0600100–107. 10.1177/1934578x0600100204

  • CrossRef
  • Google Scholar

• 35

  KumarA.LingaduraiS.JainA.BarmanN. R. (2010). Erythrina variegata Linn: a review on morphology, phytochemistry, and pharmacological aspects. Pharmacogn. Rev.4 (8), 147–152. 10.4103/0973-7847.70908

  • CrossRef
  • Google Scholar

• 36

  KumarS.PathaniaA. S.SaxenaA. K.VishwakarmaR. A.AliA.BhushanS. (2013). The anticancer potential of flavonoids isolated from the stem bark of Erythrina suberosa through induction of apoptosis and inhibition of STAT signaling pathway in human leukemia HL-60 cells. Chem. Biol. Interact.205 (2), 128–137. 10.1016/j.cbi.2013.06.020

  • CrossRef
  • Google Scholar

• 37

  LiX. L.SuiL.LinF. H.LianY.AiL. Z.ZhangY. (2019). Differential effects of genistein and 8-prenylgenistein on reproductive tissues in immature female mice. Pharm. Biol.57 (1), 226–230. 10.1080/13880209.2019.1590422

  • CrossRef
  • Google Scholar

• 38

  MachadoR. J.MonteiroN. K.MiglioloL.SilvaO. N.PintoM. F.OliveiraA. S.et al (2013). Characterization and pharmacological properties of a novel multifunctional Kunitz inhibitor from Erythrina velutina seeds. PLoS One8 (5), e63571. 10.1371/journal.pone.0063571

  • CrossRef
  • Google Scholar

• 39

  MalkowskiM. G.GinellS. L.SmithW. L.GaravitoR. M. (2000). The productive conformation of arachidonic acid bound to prostaglandin synthase. Sci. (New York, N.Y.)289 (5486), 1933–1937. 10.1126/science.289.5486.1933

  • CrossRef
  • Google Scholar

• 40

  MarumeA.MatopeG.KatsandeS.KhozaS.MutingwendeI.MduluzaT.et al (2017). Wound healing properties of selected plants used in ethnoveterinary medicine. Front. Pharmacol.8, 544. 10.3389/fphar.2017.00544

  • CrossRef
  • Google Scholar

• 41

  MeenaA. K.MotiwaleM.IlavarasanR.PerumalA.SinghR.SrikanthN.et al (2022). Evaluation of substitution of small branches with roots of Desmodium gangeticum (physicochemical analysis, HPLC, and GC-MS profiling) and in silico study of pterocarpans for pharmacological target. Appl. Biochem. Biotechnol.194 (4), 1527–1545. 10.1007/s12010-021-03696-5

  • CrossRef
  • Google Scholar

• 42

  MillsS.BoneK. (Editors) (2005). The essential guide to herbal safety (USA: Churchill Livingstone).

  • Google Scholar

• 43

  MollelJ. T.SaidJ. S.MasaluR. J.HannounC.MbundeM. V. N.NondoR. S. O.et al (2022). Anti-respiratory syncytial virus and anti-herpes simplex virus activity of six Tanzanian medicinal plants with extended studies of Erythrina abyssinica stem bark. J. Ethnopharmacol.292, 115204. 10.1016/j.jep.2022.115204

  • CrossRef
  • Google Scholar

• 44

  MujahidM.HussainT.SiddiquiH. H.HussainA. (2017). Evaluation of hepatoprotective potential of Erythrina indica leaves against antitubercular drugs induced hepatotoxicity in experimental rats. J. Ayurveda Integr. Med.8 (1), 7–12. 10.1016/j.jaim.2016.10.005

  • CrossRef
  • Google Scholar

• 45

  MuthukrishnanS.PalanisamyS.SubramanianS.SelvarajS.MariK. R.KuppulingamR. (2016). Phytochemical profile of Erythrina variegata by using high-performance liquid chromatography and gas chromatography-mass spectroscopy analyses. J. Acupunct. Meridian Stud.9 (4), 207–212. 10.1016/j.jams.2016.06.001

  • CrossRef
  • Google Scholar

• 46

  NamkoongS.KimT. J.JangI. S.KangK. W.OhW. K.ParkJ. (2011). Alpinumisoflavone induces apoptosis and suppresses extracellular signal-regulated kinases/mitogen activated protein kinase and nuclear factor-κB pathways in lung tumor cells. Biol. Pharm. Bull.34 (2), 203–208. 10.1248/bpb.34.203

  • CrossRef
  • Google Scholar

• 47

  NyandoroS. S.MunissiJ. J.KomboM.MginaC. A.PanF.GruhonjicA.et al (2017). Flavonoids from Erythrina schliebenii. J. Nat. Prod.80 (2), 377–383. 10.1021/acs.jnatprod.6b00839

  • CrossRef
  • Google Scholar

• 48

  OzawaM.KawamataS.EtohT.HayashiM.KomiyamaK.KishidaA.et al (2010). Structures of new erythrinan alkaloids and nitric oxide production inhibitors from Erythrina crista-galli. Chem. Pharm. Bull.58 (8), 1119–1122. 10.1248/cpb.58.1119

  • CrossRef
  • Google Scholar

• 49

  PancheA. N.DiwanA. D.ChandraS. R. (2016). Flavonoids: an overview. J. Nutr. Sci.5, e47. 10.1017/jns.2016.41

  • CrossRef
  • Google Scholar

• 50

  PhukhatmuenP.MeesakulP.SuthiphasilpV.CharoensupR.ManeeratT.CheenprachaS.et al (2021). Antidiabetic and antimicrobial flavonoids from the twigs and roots of Erythrina subumbrans (Hassk.) Merr. Heliyon7 (4), e06904. 10.1016/j.heliyon.2021.e06904

  • CrossRef
  • Google Scholar

• 51

  RasulA.KhanM.YuB.MaT.YangH. (2011). Xanthoxyletin, a coumarin induces S phase arrest and apoptosis in human gastric adenocarcinoma SGC-7901 cells. Asian Pac J. Cancer Prev.12 (5), 1219–1223. PMID: 21875271.

  • Google Scholar

• 52

  RosdiantoA. M.PuspitasariI. M.LesmanaR.LevitaJ. (2020). Determination of quercetin and flavonol synthase in Boesenbergia rotunda rhizome. Pak J. Biol. Sci.23, 264–270. 10.3923/pjbs.2020.264.270

  • CrossRef
  • Google Scholar

• 53

  RukachaisirikulT.InnokP.AroonrerkN.BoonamnuaylapW.LimrangsunS.BoonyonC.et al (2007a). Antibacterial pterocarpans from Erythrina subumbrans. J. Ethnopharmacol.110 (1), 171–175. 10.1016/j.jep.2006.09.022

  • CrossRef
  • Google Scholar

• 54

  RukachaisirikulT.SaekeeA.TharibunC.WatkuolhamS.SuksamrarnA. (2007b). Biological activities of the chemical constituents of Erythrina stricta and Erythrina subumbrans. Arch. Pharm. Res.30 (11), 1398–1403. 10.1007/BF02977363

  • CrossRef
  • Google Scholar

• 55

  RyuY. B.Curtis-LongM. J.KimJ. H.JeongS. H.YangM. S.LeeK. W.et al (2008). Pterocarpans and flavanones from Sophora flavescens displaying potent neuraminidase inhibition. Bioorg Med. Chem. Lett.18, 6046–6049. 10.1016/j.bmcl.2008.10.033

  • CrossRef
  • Google Scholar

• 56

  SadgroveN. J.OliveiraT. B.KhumaloG. P.VuurenS. F. V.van WykB. E. (2020). Antimicrobial isoflavones and derivatives from Erythrina (Fabaceae): structure-activity perspective (SAR & QSAR) on experimental and mined values against Staphylococcus aureus. Antibiot. (Basel)9 (5), 223. 10.3390/antibiotics9050223

  • CrossRef
  • Google Scholar

• 57

  SelvamC.JachakS. M.OliR. G.ThilagavathiR.ChakrabortiA. K.BhutaniK. K. (2004). A new cyclooxygenase (COX) inhibitory pterocarpan from Indigofera aspalathoides: structure elucidation and determination of binding orientations in the active sites of the enzyme by molecular docking. Tetrahedron Lett.45 (22), 4311–4314. 10.1016/j.tetlet.2004.04.010

  • CrossRef
  • Google Scholar

• 58

  Setti-PerdigãoP.SerranoM. A.FlausinoO. A.JrBolzaniV. S.GuimarãesM. Z.CastroN. G. (2013). Erythrina mulungu alkaloids are potent inhibitors of neuronal nicotinic receptor currents in mammalian cells. PLoS One8 (12), e82726. 10.1371/journal.pone.0082726

  • CrossRef
  • Google Scholar

• 59

  Silveira-SoutoM. L.São-MateusC. R.de Almeida-SouzaL. M.GroppoF. C. (2014). Effect of Erythrina mulungu on anxiety during extraction of third molars. Med. Oral, Patol. Oral Cirugia Bucal19 (5), e518–e524. 10.4317/medoral.19511

  • CrossRef
  • Google Scholar

• 60

  SimãoTLBVAguiarG. V.RamosA. C.SilvaG. P. D.MuzitanoM. F.LassounskaiaE.et al (2022). Antimycobacterial and anti-inflammatory activities of fractions and substances from Erythrina verna Vell focusing on dual severe TB treatment approach. Acad Bras Cienc94 (3), e20211032. 10.1590/0001-3765202220211032

  • CrossRef
  • Google Scholar

• 61

  SkorobogatovV. I. (1967). The central action of curarizing drugs. Prog. Brain Res.20, 243–255. 10.1016/S0079-6123(08)62897-6

  • CrossRef
  • Google Scholar

• 62

  Standard Process (2023). Herb-drug interaction Chart. Available at: https://my.standardprocess.com/MediHerb-Document-Library/Catalog-Files/herb-drug-interaction-chart.pdfAccessedonSeptember30.

  • Google Scholar

• 63

  StromsnesK.LagzdinaR.Olaso-GonzalezG.Gimeno-MallenchL.GambiniJ. (2021). Pharmacological properties of polyphenols: bioavailability, mechanisms of action, and biological effects in in vitro studies, animal models, and humans. Biomedicines9 (8), 1074. 10.3390/biomedicines9081074

  • CrossRef
  • Google Scholar

• 64

  SunL. P.GaoL. X.MaW. P.NanF. J.LiJ.PiaoH. R. (2012). Synthesis and biological evaluation of 2,4,6-trihydroxychalcone derivatives as novel protein tyrosine phosphatase 1B inhibitors. Chem. Biol. Drug Des.80 (4), 584–590. 10.1111/j.1747-0285.2012.01431.x

  • CrossRef
  • Google Scholar

• 65

  UddinM. M.EmranT. B.MahibM. M.DashR. (2014). Molecular docking and analgesic studies of Erythrina variegata׳s derived phytochemicals with COX enzymes. Bioinformation10 (10), 630–636. 10.6026/97320630010630

  • CrossRef
  • Google Scholar

• 66

  UnnaK.GreslinJ. G. (1943). Pharmacologic Action of Erythrina alkaloids. Chapter II. Free, liberated and combined alkaloids. Rahway, New Jersey: From the Merck Institute for Therapeutic Research. Available at: https://citeseerx.ist.psu.edu/document?repid=rep1&type=pdf&doi=8e62f8bf46b2cb81d51b54b44930028623dac807.

  • Google Scholar

• 67

  VecchioA. J.SimmonsD. M.MalkowskiM. G. (2010). Structural basis of fatty acid substrate binding to cyclooxygenase-2. J. Biol. Chem.285 (29), 22152–22163. 10.1074/jbc.M110.119867

  • CrossRef
  • Google Scholar

• 68

  VenturiS.MarinoM.CioffiI.MartiniD.Del Bo'C.PernaS.et al (2023). Berry dietary interventions in metabolic syndrome: new insights. Nutrients15 (8), 1906. 10.3390/nu15081906

  • CrossRef
  • Google Scholar

• 69

  WaiganjoB.MoriasiG.OnyanchaJ.EliasN.MuregiF. (2020). Antiplasmodial and cytotoxic activities of extracts of selected medicinal plants used to treat malaria in Embu County, Kenya. J. Parasitol. Res.2020, 8871375. 10.1155/2020/8871375

  • CrossRef
  • Google Scholar

• 70

  WätjenW.KulawikA.Suckow-SchnitkerA. K.ChovolouY.RohrigR.RuhlS.et al (2007). Pterocarpans phaseollin and neorautenol isolated from Erythrina addisoniae induce apoptotic cell death accompanied by inhibition of ERK phosphorylation. Toxicology242 (1-3), 71–79. 10.1016/j.tox.2007.09.010

  • CrossRef
  • Google Scholar

• 71

  WedickN. M.PanA.CassidyA.RimmE. B.SampsonL.RosnerB.et al (2012). Dietary flavonoid intakes and risk of type 2 diabetes in US men and women. Am. J. Clin. Nutr.95 (4), 925–933. 10.3945/ajcn.111.028894

  • CrossRef
  • Google Scholar

• 72

  WondmkunY. T. (2020). Obesity, insulin resistance, and type 2 diabetes: associations and therapeutic implications. Diabetes Metab. Syndr. Obes.13, 3611–3616. 10.2147/DMSO.S275898

  • CrossRef
  • Google Scholar

• 73

  XiaoH. H.YuX.YangC.ChanC. O.LuL.CaoS.et al (2021). Prenylated isoflavonoids-rich extract of Erythrinae cortex exerted bone protective effects by modulating gut microbial compositions and metabolites in ovariectomized rats. Nutrients13 (9), 2943. 10.3390/nu13092943

  • CrossRef
  • Google Scholar

• 74

  XingX.MaJ. H.FuY.ZhaoH.YeX. X.HanZ.et al (2019). Essential oil extracted from Erythrina corallodendron L. leaves inhibits the proliferation, migration, and invasion of breast cancer cells. Med. Baltim.98 (36), e17009. 10.1097/md.0000000000017009

  • CrossRef
  • Google Scholar

• 75

  YenesewA.DereseS.MidiwoJ. O.BiiC. C.HeydenreichM.PeterM. G. (2005). Antimicrobial flavonoids from the stem bark of Erythrina burttii. Fitoterapia76 (5), 469–472. 10.1016/j.fitote.2005.04.006

  • CrossRef
  • Google Scholar