REVIEW article

Front. Pharmacol., 09 September 2022

Sec. Inflammation Pharmacology

Volume 13 - 2022 | https://doi.org/10.3389/fphar.2022.974794

Compounds purified from edible fungi fight against chronic inflammation through oxidative stress regulation

  • 1. Department of Hand and Foot Surgery, The First Hospital of Jilin University, Changchun, China

  • 2. Laboratory Animal Center, College of Animal Science, Jilin University, Changchun, China

Abstract

Chronic inflammation is associated with various chronic diseases, including cardiovascular disease, neurodegenerative disease, and cancer, which severely affect the health and quality of life of people. Oxidative stress induced by unbalanced production and elimination of reactive oxygen species (ROS) is one of the essential risk factors for chronic inflammation. Recent studies, including the studies of mushrooms, which have received considerable attention, report that the antioxidant effects of natural compounds have more advantages than synthetic antioxidants. Mushrooms have been consumed by humans as precious nourishment for 3,000 years, and so far, more than 350 types have been identified in China. Mushrooms are rich in polysaccharides, peptides, polyphenols, alkaloids, and terpenoids and are associated with several healthy biological functions, especially antioxidant properties. As such, the extracts purified from mushrooms could activate the expression of antioxidant enzymes through the Keap1/Nrf2/ARE pathway to neutralize excessive ROS and inhibit ROS-induced chronic inflammation through the NF-κB pathway. Recently, the antioxidant properties of mushrooms have been successfully applied to treating cardiovascular disease (CAD), neurodegenerative diseases, diabetes mellitus, and cancer. The present review summarizes the antioxidant properties and the mechanism of compounds purified from mushrooms, emphasizing the oxidative stress regulation of mushrooms to fight against chronic inflammation.

Introduction

Mushrooms have been extensively cultivated in China using artificial techniques due to their high yield, desirable taste, and widespread consumption and application as a medicinal resource (). Recently, various compounds have been isolated from mushrooms, such as polysaccharides, alkaloids, peptides, terpenoids, and polyphenols (; ; ; ; ). Mushroom extracts can resist free radicals, reduce the activities of pro-inflammatory factors, and relieve chronic inflammation, which are valuable natural antioxidants with the advantages of safety, nontoxic, and easy to obtain (). Some studies have also demonstrated the therapeutic potential of mushroom extract for cardiovascular disease (CAD), neurodegenerative diseases, and cancer (; ; ). This review discusses the mechanisms underlying the effect of oxidative stress on chronic inflammation and summarizes the antioxidant properties of compounds purified from mushrooms. The anti-inflammatory effects of these compounds on CAD, neurodegenerative diseases, diabetes mellitus, and cancer provide potential treatment measures for chronic inflammation caused by oxidative stress.

Chronic inflammation and oxidative stress

Predisposing factors of oxidative stress

The predisposing factors, including diet, exercise, chemicals, radiation, and drugs, can increase reactive oxygen species (ROS) production and disrupt the antioxidant system, inducing oxidative stress (; ; ; ). Similarly, eating habits, including refined carbohydrates, high-fat, and high-animal protein diets, can increase oxidative stress through the nuclear factor-kappa B (NF-κB) signaling pathways (). High sugar intake can produce advanced glycation end products to promote oxidation and activate the protein phosphatase 2 A and NF-κB pathways, inducing oxidative stress in mitochondria (). Regular and moderate exercise has also been proven to inhibit ROS production, while high intensity and long-term exercise might induce oxidative stress in the skeletal muscle cells, causing muscle contractile dysfunction (; ). A previous study has reported that the exposure of cells to metals and metal oxide nanoparticles induces oxidative stress, thereby damaging the deoxyribonucleic acids (DNAs), proteins, and lipids (). For instance, aluminum accumulation could impair the oxidative function of mitochondria, especially in the brain, which is explicitly sensitive to oxidative stress and is one of the causes of neurodegenerative diseases (). Similarly, continuous exposure to ionizing radiation induces excessive production of hydroxyl radicals through water oxidation or secondary partially ROS formation (). Drugs, including gentamicin and bleomycin, could produce free radicals during degeneration and metabolism (). Additionally, the potential predisposing factors, including unhealthy living habits, exposure to harmful substances, and certain drugs, could induce oxidative stress and damage the cellular components through different mechanisms.

Mechanism of oxidative stress

In mitochondria, most oxygen is utilized for aerobic respiration and energy release, with ROS being produced as a byproduct (). Mitochondria convert glucose to adenosine triphosphate (ATP) through the tricarboxylic acid cycle and oxidative phosphorylation by using nicotinamide adenine dinucleotide (NADH) and reduced flavin adenosine dinucleotide (FADH2) produced in the cytoplasmic matrix (). In the oxidative phosphorylation process, NADH and FADH2 efficiently reduce oxygen and release energy through the electron transport chain (ETC) (). However, a small quantity of oxygen is still reduced prematurely by electrons, producing superoxide anion (O2), a relatively stable intermediate, which can generate hydrogen peroxide (H2O2) by disproportionation reaction, or hydroxyl radicals (OH) by the Haber-Weiss and Fenton reaction (Figure 1) ().

FIGURE 1

Under physiological conditions, ROS can be removed by the antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-PX), and peroxiredoxin/thioredoxin (Prx/Trx) (). SOD consists of manganese superoxide dismutase (MnSOD) located in the mitochondrial matrix and cuprum/zinc superoxide dismutase (Cu/ZnSOD) in the membrane gap, which can dismutate the O2—produced by ETC into H2O2 (). The GSH-PX and Prx/Trx systems of the cytoplasmic matrix could reduce H2O2, while nicotinamide adenine dinucleotide phosphate (NADPH) maintains the reducing power of these two antioxidant systems (). Meanwhile, NADH/NADPH oxidase serves as an intracellular ROS source, especially in the vascular tissues and cardiomyocytes (). The persistence of ROS damages the somatic cells, including the cardiac muscle cells and nerve cells, while the antioxidant properties of the compounds in mushrooms neutralize the ROS ().

Mechanism of oxidative stress in chronic inflammation

The persistence of inflammatory factors causing tissue damage, such as trauma, chemical erosion, microbial infection, and autoimmune reaction, significantly contributes to chronic inflammation (; ). When inflammation occurs, oxygen uptake by the white blood cells and mast cells in the inflammatory area increases, leading to “respiratory burst,” which enhances ROS production and release (). It is reported that low density lipoprotein (LDL) can be oxidized by ROS and phagocytosed by macrophages, thereby improving the release of pro-inflammatory factors and inducing inflammatory responses mediated by the NF-κB signal pathway (). The expression of phagocytic NADPH oxidase relying on NF-κB could produce ROS and increase the bactericidal activity of macrophages through the Toll-like receptors, including Toll-like receptor 1 (TLR1), TLR2, and TLR4 (). However, excessive intracellular ROS stimulate the expression of NF-κB by activating the p38 signaling pathway and regulating the liberation of pro-inflammatory factors, including tumor necrosis factor-α (TNF-α), inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2) (). Additionally, ROS could stimulate the expression of TLR4 and trigger an inflammatory response in the lungs by activating the NF-κB pathway (). Oxidative stress can induce chronic inflammation, while the inflammatory response can improve ROS release, primarily mediated through the NF-κB signal pathway (Figure 2).

FIGURE 2

Antioxidant effects and mechanisms of compounds purified from edible fungi

Extraction of compounds from edible fungi

Mushrooms are rich in polysaccharides, peptides, polyphenols, and other compounds beneficial to human health. Hence, mushrooms have been widely recognized as functional food resources and are being used for developing drugs and nutrients (). In recent years, mushroom-derived polysaccharides have gained considerable attention due to their antioxidant, antibacterial, anti-tumor, and immunomodulatory effects (). Most of the polysaccharides from mushrooms are water-soluble and can be extracted frequently by water extraction using heating, ultrasound, and microwave techniques (). According to modern technology, water extraction has some disadvantages, such as long extraction time, low efficiency, and risk of biopolymer degradation. As such, the subcritical pressurized hot water extraction technology and deep eutectic solvent extraction technology have emerged as potential approaches to achieving efficient water extraction (). Extracting mushroom-derived bioactive peptides is mostly dependent on the proteolytic action of exogenous enzymes and microbial fermentation technology (). Traditionally, microwave-assisted and ultrasound-assisted methods were used to extract the phenolic compounds (). Different extraction methods may influence the antioxidant effects of different compounds in mushrooms, thus helping to select the appropriate extraction method to inhibit chronic inflammation by eliminating ROS.

Polysaccharide

Polysaccharide, the most widely studied compound in mushrooms, is primarily composed of more than 10 monosaccharides linked with glycosidic bonds of polymeric sugar polymer carbohydrates (Supplementary Figure.S1) (). The hydrogen ion on the sugar chain of polysaccharides can directly bind to OH and break down into harmless products (). Polysaccharides can inhibit oxidative stress by improving the activities of antioxidant enzymes, including SOD, CAT, and GSH-PX, or chelate with metal ions, essential for ROS production (). The antioxidant effect of polysaccharides is mainly mediated through the activation of the Keap1/Nrf2/ARE pathway to achieve the expression of downstream antioxidant enzymes (Figure 3A) (). Nuclear factor erythroid-2 (Nrf2) is the major regulatory element of the antioxidant system in vivo, which can detach from the binding site of Kelch-like ECH-associated protein 1 (Keap1) in the cytoplasm after being stimulated and transferred to the nucleus to bind with the anti-oxidant response element (ARE) (). Polysaccharides have been reported to regulate oxidative stress by upregulating the expression of phosphatidylinositol 3-kinase (P13K) and phosphorylation of protein kinase B (AKT) ().

FIGURE 3

Poria cocos polysaccharide could eliminate O2—and OH, while carboxymethylated pachymaran could promote the expression of SOD to achieve an antioxidant effect (). Lepista nuda polysaccharides extracted through water extraction and alcohol precipitation method could chelate iron ions and scavenge O2—and 1,1-diphenyl-2-picrylhydrazyl free (DPPH) radicals and in a concentration-dependent manner (). A water-soluble polysaccharide isolated from the alkaline extract of Entoloma lividoalbum could eliminate OH through the hydrogen atom donation ability of its hydroxyl group (). In a previous study, the ultrasonic-assisted extraction of Flammulina velutipes polysaccharide showed stronger scavenging ability of DPPH, OH, and O2—than hot water extraction, with better inflammation inhibitory ability (). For instance, the polysaccharide purified for the first time from the floral mushrooms cultivated in Huangshan could scavenge 79.46% DPPH free radical and 74.18% OH at 5 mg/ml (). A new polysaccharide AAP-3-1 isolated from the fruit body of Auricularia auricula could inhibit ROS production, reduce malondialdehyde content, and increase the activities of SOD, GSH-PX, and CAT ().

Peptides

Peptides are composed of three or more amino acid molecules linked by peptide bonds, which can be easily absorbed by the intestine and pose excellent physiological characteristics than proteins (). The aromatic amino acids and hydrophobic amino acid residues in the peptides could significantly increase the antioxidant activity, thereby inducing hydrogen atoms (; ). Peptides can activate the Nrf2 pathway by downregulating the Keap1 gene and upregulating the Nrf2 gene expression to achieve antioxidant effects (Figure 3B) (). Mushrooms are the primary sources of natural active peptides with significant potency, high tissue affinity, low toxicity, and high stability (). An analysis of the GSH levels in various mushroom species showed that the GSH content of Maitake was higher than most fruits and vegetables, indicating that mushrooms could be an indispensable source of GSH in the daily diet (). In a previous study, Matsutake derived peptide WFNNAGP significantly inhibited glucan sulfate-induced oxidative stress in mice by scavenging OH and promoting the SOD activity, thereby preventing colon inflammation (). Low molecular weight peptides decomposed from the protein hydrolysates of Agaricus bisporus by enzymatic processes are abundant in negatively charged amino acids, which can be applied to neutralize free radicals to resist oxidative stress ().

Polyphenol

Polyphenols consisting of at least one aromatic ring with hydroxyl functional groups, including flavonoids, phenolic acids, stilbenes, and lignans, are the natural antioxidants in plant foods (). Polyphenols can provide electrons or hydrogen atoms to neutralize free radicals or chelate with metal ions to reduce the rate of Fenton reaction (Figure 3C) (). Agaricus brasiliensis mushroom containing phenolic compounds, such as gallic acid, serum acid, and pyrogallol, could inhibit ROS production by tert-butyl hydrogen peroxide stimulated macrophages (). A novel polyphenol isolated from Phellinus linteus hispolon and its derivatives has been reported to have a strong free radical scavenging ability (). In a previous study, the release of phenolic compounds in agaricus bisporus, cantharellus cibarius, and lentinula edodes was determined by the simulating human gastrointestinal digestion method. The results indicated that lentinus edodes released the most phenolic acids, confirming that the phenolic compounds in lentinus edodes might easily improve the antioxidant capacity of the human body through consumption (). Meanwhile, the flavonoids purified from Flammulina velutipes significantly increased the glutathione level, and the SOD activity of PC12 cells efficiently inhibited intracellular ROS accumulation (). The phenolic compounds in the water extract of lentinus edobes and methanol extract of volvariella volvacea showed a higher hydrogen-providing ability to scavenge the DPPH radicals ().

Proteins, terpenoids, arene, and lipids

Polysaccharides, polypeptides, and polyphenols are the major antioxidant compounds in mushrooms, while other compounds, including proteins, terpenes, arene, and lipids, tend to have antioxidant properties (). A novel protein from edible fungi could effectively remove OH and DPPH in vitro, while promoting the apoptosis of breast cancer cells through anti-tumor activity (). Terpenoids isolated and identified from Sanghuangporus sanghuang could scavenge DPPH and 2,2′-Azinobis-(3-ethylbenzthiazoline-6-sulphonate) (ABTS) free radicals; however, their antioxidant activity is significantly inferior to the polysaccharides and phenolic compounds (). P-terphenyl compounds isolated from mushroom Boletopsis leucomelas through chromatography possess effective DPPH scavenging capacity, which can be enhanced with heating (). 2,5-diarylcyclopentenone derivatives from Paxillus involutus possess clearing abilities of DPPH,·OH, and O2—(). Mushrooms are rich in fatty acids, much higher than in beef and pork, which might contribute to their antioxidant ability to fight against mitochondrial dysfunction (; ).

The antioxidant properties of compounds purified from mushrooms are affected by species, the extracted parts, and purification methods. Accumulating researchers have studied the polysaccharides, peptides, and phenolic compounds comprehensively, while studies focusing on protein, terpenoids, arene, and fatty acids are limited. The antioxidant effects of different compounds in mushrooms are presented in Table 1.

TABLE 1

MushroomsCompoundsNameAntioxidant effectsReferences
Lepista nudaPolysaccharideLNPScavenge DPPH and O2·-
Entoloma lividoalbumPolysaccharideELPSEliminate ·OH
Flammulina velutipesPolysaccharideFVPsScavenge DPPH, ·OH, and O2·-
Floral mushroomPolysaccharideFMPSScavenge DPPH and ·OH
Auricularia auriculaPolysaccharideAAP-3-1Increase the activities of SOD, GSH-PX, and CAT
Oyster mushroomPolysaccharideExtractImprove the antioxidant status during ageing
Pleurotus ostreatusPolysaccharideExtractProtect against oxidative damage induced by H2O2
Pleurotus djamorPolysaccharideExtractScavenge DPPH and ·OH
Pleurotus eryngiiPolysaccharidePERPScavenge reactive radicals and improve the antioxidant status
Hohenbuehelia serotinaPolysaccharideNTHSP-A1Scavenging abilities of ABTS radical and ·OH radical
MaitakePeptideGlutathioneAntioxidant property
MatsutakePeptideWFNNAGPScavenge ·OH and promote the SOD activity
Agaricus bisporusPeptideMPINeutralize free radicals to resist oxidative stress
Schizophyllum communePeptideExtractFree radical scavenging activity
Ophiocordyceps sinensisPeptideCOPScavenge DPPH radical and chelate heavy metal ions
Hericium erinaceusPeptideExtractABTS, DPPH and NO radical scavenging activities
Agaricus blazeiPeptideABpChange the contents of T-AOC, MDA, CAT, and ROS
Pleurotus eryngiiPeptidePEMPScavenge DPPH, ·OH, and O2·- radicals
Sanghuangporus sanghuangPolyphenolExtractGood cellular antioxidant activities
Flammulina velutipesPolyphenolFFVPInhibit the secretion of NO and ROS
Phlebopus portentosusPolyphenolExtractDPPH scavenging activity and ferric reducing antioxidant power
Phellinus linteusPolyphenolHispolonStrong free radical scavenging ability
Flammulina velutipesPolyphenolFVFIncrease glutathione level and SOD activity and inhibit the accumulation of intracellular ROS
Boletus edulis and Cantharellus cibariusPolyphenolExtractThe aqueous extract showed the strongest antioxidant activity
Sanghuangporus baumiiPolyphenolExtractScavenge ·OH, DPPH, and ABTS
Boletopsis leucomelasP-terphenyl compoundExtractEffective DPPH scavenging capacity
T. terrestris and T. vialisP-terphenyl compoundExtractPrevent VEGF-induced production of ROS and malondialdehyde
Hericium erinaceumSterolExtractCellular antioxidant activity
Pholiota namekoProteinPNAPScavenge ·OH and DPPH
Sanghuangporus sanghuangTerpenoidExtractScavenge DPPH and ABTS free radicals
Paxillus involutus2,5-diarylcyclopentenoneExtractClearing abilities of DPPH, ·OH, and O2·-
AgaricomycetesExtractExtractSignificantly increase the activities of SOD, CAT and GSH-Px
Agaricus bisporusExtractExtractEnhance the activities of antioxidant enzymes
Lactarius salmonicolorExtractExtractShow the most potent radical scavenging activity
Ramaria flavaExtractExtractHigh DPPH and ·OH radical-scavenging activities
ChagaExtractExtractScavenging activity against the ABTS radical cation and DPPH radical.
Porodaedalea chrysolomaExtractExtractPossess considerable antioxidant effect
Orange coral mushroomExtractExtractGood free radical scavenges and reduce capacities
Cynomorium coccineumExtractExtractORAC-PYR assay gives the highest antioxidant value in both cases
Entoloma lividoalbumExtractExtractPossess hydroxyl and superoxide radical-scavenging activities
Flammulina velutipesExtractExtractHigh DPPH radical scavenging activity
Pleurotus ostreatusExtractExtractHigh DPPH and hydrogen peroxide scavenging potential
Agaricus brasiliensisExtractExtractProtect against sepsis by alleviating oxidative and inflammatory response

Antioxidant effects of compounds purified from mushrooms.

Applications of mushroom-derived compounds on chronic inflammatory diseases

Cardiovascular disease

Endothelial cells act as the barrier between the blood and blood vessel wall, mediating the synthesis and release of a series of active substances (). Oxidative stress associated with increased ROS production and reduced nitric oxide (NO) availability in the blood vessels and myocardium could induce endothelial dysfunction, including impaired vasodilation, proinflammatory, and thrombogenic, a risk factor for cardiovascular disease (). Endothelial-derived NO is the primary vasodilator and can react with increased ROS to form toxic peroxynitrite (ONOO−) (). Meanwhile, ROS can induce the uncoupling of endothelial NO synthase (eNOS), a vital enzyme for NO production (). The mushroom-derived compounds exert antioxidant effects through the Nrf2 pathway to effectively treat chronic cardiovascular diseases caused by endothelial disorders (; ) (Figure 4A).

FIGURE 4

Ergothioneine is highly abundant in mushrooms and has the ability to scour ROS and chelate the metal cations. This phenomenon of ergothioneine could effectively regulate endovascular inflammation caused by endothelial dysfunction and reduce the release of pro-inflammatory factors, including interleukin-6 (IL-6), IL-1β, and TNF-α (). The water-soluble polysaccharide FC isolated from wild mushroom agaricus bitorquis could inhibit the NADPH oxidase activity, which might be used to treat myocardial infarction, hypertension, and atherosclerosis caused by excessive ROS (). In a previous study, the vasodilatation of phellinus linteus extracts was found in the rat mesenteric artery, which might induce the antioxidant and anti-inflammatory effects of polysaccharides, peptides, and terpenoids in the mycelium (; ; ).

Neurodegenerative disease

Neurodegenerative diseases are characterized by the degeneration and loss of neurons in the brain and spinal cord, including Parkinson’s disease (PD), Alzheimer’s disease (AD), and Huntington’s disease (). Lipids in the brain play a vital role in the function of neurons, which are vulnerable to being attacked by ROS and produce lipid peroxidation to form malondialdehyde (MDA), inducing reduced membrane fluidity and neuron degeneration (). Meanwhile, the damaged neurons activate microglia and astrocytes to release the pro-inflammatory cytokines and ROS, further exacerbating neurodegeneration (). ROS produced by oxidative stress could damage and mutate the mitochondrial DNA, increasing oxidative decomposition of dopamine as the pathogenesis of neurodegenerative diseases and the accumulation of abnormal protein, such as amyloid beta (Aβ) in AD (Figure 4B) (). Antioxidants in mushrooms could directly neutralize ROS or activate the Nrf2/ARE signaling pathway to induce the competence of antioxidant enzymes ().

Ethanol extracts from hericium erinaceus could alleviate the mitochondrial damage caused by H2O2 and activate antioxidant enzymes to treat hippocampal neurons’ injury in mice (). The polysaccharide peptides and vitamins in coriolus versicolor could significantly reduce the proportion of GSH and oxidized glutathione (GSSG) in the plasma to relieve the systemic oxidative stress state and nerve injury of patients (). Meroterpenoids from Albatrellus yasudae have been found to inhibit Aβ aggregation, which might be a therapeutic and health care product for AD (). Polyphenols, polysaccharides, and triterpenes in Amauroderma rugosum could reduce oxidative stress and 6-hydroxydopamine-induced mitochondria dysfunction in the PC12 cells ().

Diabetes mellitus

The occurrence of diabetes mellitus is related to the dysfunction of islet β cells and insulin resistance, in which oxidative stress plays a vital role in regulating multiple signaling pathways (). Excessive ROS can activate the NF-κB, JNK/SAPK, and p38 MAPK pathways by activating TLR and inducing the dysfunction of islet β cells (). A persistent hyperglycemic environment induces ROS production through the binding of advanced glycation end products (AGE) to peroxisome proliferators activated receptors (PPAR) (). Additionally, excessive production of AGE increases the expression of inflammatory mediators through the NF-κB pathway (). The inflammatory factor TNF-α activates the intracellular signaling factor IKKβ that affects insulin production through the NF-κB signaling pathway (; ).

Polysaccharides isolated from Inonotus obliquus are the potential to treat type 2 diabetes by directly removing ROS or mediating lipid peroxidation (). Terpenoids from Antrodia camphorata could significantly inhibit the binding of AGE to PPAR and reduce blood glucose levels, thus inhibiting ROS production and promoting insulin secretion (). Alkali-soluble polysaccharides from Amillariella mellea could improve pancreatic B-cell dysfunction caused by oxidative stress, thereby improving insulin sensitivity and reducing insulin resistance (). As food supplements, P. Ostreatus and L. Subnudus have been shown to increase the activity of antioxidant enzymes and non-enzymatic antioxidants, inducing memory loss in diabetic rats ().

Cancer

ROS can induce chronic inflammation, and the continuous inflammatory environment and oxidative stress might damage the adjacent epithelial cells and stromal cells, inducing cancer (). Additionally, ROS induces the proliferation of cancer cells and promotes tumor growth by activating the MAPK pathway (). Tumor cell metastasis depends on the epithelial-mesenchymal transformation process, in which ROS activates the proteins, including β -catenin, e-cadherin, and matrix metalloproteinases (MMP), through the Wnt/β -catenin signaling pathway ().

Termitomyces Clypeatus significantly inhibited the tumor volume and number of ascites carcinoma mice by inhibiting lipid peroxidation and increasing the levels of GSH, SOD, and CAT (). The extracts from Lactarius deliciosus and Coprinus comatus inhibited the activity of MMP produced by oxidative stress and induced apoptosis in gliomas associated with G1 or G2/M phase cell cycle stagnation (). Natural antioxidants isolated from Thelephora Ganbajun by ultrasonic-assisted technology exhibited anti-proliferation effects on the liver and lung cancer cells (). Antrodia salmonea induces protective autophagy and apoptosis in colon cancer cells through cascades of extracellular signal kinase (ERK) signaling, which has been reported to mediate ROS due to the double-sided effects of antioxidants on cancer cells (; ).

The compounds purified from mushrooms might possess promising applications in preventing and treating cardiovascular diseases, neurodegenerative diseases, and cancer by regulating oxidative stress and chronic inflammation.

Discussion

Excessive ROS increases the release of pro-inflammatory factors, thereby promoting ROS production, which is the primary reason for oxidative stress-induced chronic inflammation. Chronic inflammation can lead to organic diseases in different tissues and organs over time. Chronic inflammation in the blood vessels can affect the vascular endothelial relaxation function and form atherosclerosis, the root cause of coronary atherosclerotic heart disease (). It is reported that chronic inflammatory response persists in the neurodegeneration of AD and is considered an important factor in accelerating the progression (). In chronic inflammation, ROS can damage DNA and cause biological macromolecule dysfunction, such as proteins and lipids, inducing antioxidant dysfunction and a vicious cycle of oxidative stress, a risk factor for cancer (). In recent years, antioxidants have attracted much attention due to their oxidative stress combating ability to inhibit chronic inflammation. Natural compounds are more easily recognized and absorbed by the body than synthetic antioxidants, with no toxic side effects (). Chinese herbs, including Astragalus membranaceus, berberine, and curcumin have also been proven to have antioxidant properties (; ; ). The separation and purification process of Chinese herbs extract is complicated, implying that purity can affect its application. Meanwhile, improper usage might lead to toxicoses (; ). In contrast, mushrooms are widely distributed, easy to process, and can provide various nutrients with simple treatments (). Additionally, mushrooms are well absorbed by the human body with no harm as the natural antioxidant ().

Mushrooms possess many biological and pharmacological characteristics, which are already applied in nutrition, health care, and medical treatment (). Therefore, studies pay more attention to mushroom-derived polysaccharides than other compounds, as the purification method is mature and the biological activity is stable and diverse (). Mushroom polysaccharides mainly contain β-glucan chains, which have been proven to have antioxidant effects (). The hydrogen ions of mushroom polysaccharides could inhibit oxidative stress by neutralizing ROS and enhance antioxidant effects through chemical modification, including carboxymethylation and sulphuration (; ). The extraction method significantly affected the antioxidant activity of the compound. Water extraction of Lepista nuda polysaccharides showed better scavenging ability of free radicals than ethanol extraction (). The same compound had different scavenging abilities for different free radicals. For instance, Sanghuang could scavenge 68% ·OH and 57% O2—at 1 mg/ml, indicating that the scavenging ability of most compounds in the mushrooms is concentration-dependent (). Mushrooms are a promising source of natural antioxidants, ergothioneine, and glutathione, with the highest content in the mushroom cap of yellow oyster (). However, more research on different species of natural compounds purified from mushrooms should be conducted to broaden their application.

In conclusion, the compounds in mushrooms could inhibit oxidative stress and chronic inflammation by neutralizing excessive ROS or activating antioxidant enzymes through the Nrf2 signaling pathway and have been applied to cardiovascular disease, neurodegenerative disease, and cancer.

Statements

Author contributions

YX and DW wrote the manuscript. JL, MC, DW, ZJ, and BL collected the references and prepared figures. All authors reviewed the manuscript.

Funding

This research was financially supported by the National Natural Science Foundation of China (Grant Nos. 52022095, 82071391, 51973216, 51873207, and 51833010), the Provincial Health Special Project of Jilin Province (Grant Nos. JLSCZD 2019-002 and JLSWSRCZX 2020-095), the Science and Technology Development Program of Jilin Province (Grant No. 20200404182YY), the Youth Innovation Promotion Association of Chinese Academy of Sciences (Grant No. 2019230), and Natural science Foundation of the Jilin province (Grant No. 20210101310JC). Project of science and Technology Department of Jilin Province (Grant No. 20220505033ZP).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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.2022.974794/full#supplementary-material

SUPPLEMENTARY FIGURE S1

Structure of compounds purified from mushrooms, with hydrogen atoms in red as active sites against oxidative stress. N is the number of cycles. (A) Structure of mushroom polysaccharide. (B) Structure of mushroom peptides. (C) Structure of mushroom polyphenols, with flavonoids as an example.

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Summary

Keywords

chronic diseases, natural compounds, edible fungi, antioxidants, molecular mechanisms

Citation

Xia Y, Wang D, Li J, Chen M, Wang D, Jiang Z and Liu B (2022) Compounds purified from edible fungi fight against chronic inflammation through oxidative stress regulation. Front. Pharmacol. 13:974794. doi: 10.3389/fphar.2022.974794

Received

21 June 2022

Accepted

17 August 2022

Published

09 September 2022

Volume

13 - 2022

Edited by

Li Wu, Nanjing University of Chinese Medicine, China

Reviewed by

Ting Shen, Huaiyin Normal University, China

Yunyao Jiang, Tsinghua University, China

Updates

Copyright

*Correspondence: Ziping Jiang, ; Bin Liu,

† These authors have contributed equally to this work

This article was submitted to Inflammation Pharmacology, a section of the journal Frontiers in Pharmacology

Disclaimer

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.

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