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Phenolic and Steroidal Metabolites from the Cultivated Edible Inonotus hispidus Mushroom and Their Bioactivities
A chemical study on the fruiting bodies of cultivated edible mushroom Inonotus hispidus resulted in 14 metabolites including three new hispolon congeners, named inonophenols A–B and one new lanostane triterpenoid, named inonoterpene A. These structures were identified by NMR, high-resolution electro...
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Published in: | Journal of agricultural and food chemistry 2021-01, Vol.69 (2), p.668-675 |
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container_title | Journal of agricultural and food chemistry |
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creator | Kou, Rong-Wei Du, Shuang-Tian Xia, Bing Zhang, Qiang Yin, Xia Gao, Jin-Ming |
description | A chemical study on the fruiting bodies of cultivated edible mushroom Inonotus hispidus resulted in 14 metabolites including three new hispolon congeners, named inonophenols A–B and one new lanostane triterpenoid, named inonoterpene A. These structures were identified by NMR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and electronic circular dichroism (ECD) data analysis. All metabolites were assessed for neurotrophic, anti-inflammatory, and antioxidative activities. Among them, inonophenols B and C were the most active in promoting PC-12 cell neurite outgrowth at a concentration of 10 μM. The phenolic derivatives reduced NO generation by lipopolysaccharide (LPS)-induced BV-2 microglial cells by suppressing the expression of toll-like receptor-4 (TLR-4) and the nuclear factor-kappa-B (NF-κB) signaling pathway as well as the inflammatory mediators including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Moreover, the phenolics showed antioxidant effects in DPPH scavenging assay with the IC50 values of 9.82–21.43 μM. These findings showed that I. hispidus may be a new source of neurotrophic and protective agents against neurodegenerative disorders. |
doi_str_mv | 10.1021/acs.jafc.0c06822 |
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These structures were identified by NMR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and electronic circular dichroism (ECD) data analysis. All metabolites were assessed for neurotrophic, anti-inflammatory, and antioxidative activities. Among them, inonophenols B and C were the most active in promoting PC-12 cell neurite outgrowth at a concentration of 10 μM. The phenolic derivatives reduced NO generation by lipopolysaccharide (LPS)-induced BV-2 microglial cells by suppressing the expression of toll-like receptor-4 (TLR-4) and the nuclear factor-kappa-B (NF-κB) signaling pathway as well as the inflammatory mediators including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Moreover, the phenolics showed antioxidant effects in DPPH scavenging assay with the IC50 values of 9.82–21.43 μM. These findings showed that I. hispidus may be a new source of neurotrophic and protective agents against neurodegenerative disorders.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/acs.jafc.0c06822</identifier><identifier>PMID: 33398984</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Animals ; Anti-Inflammatory Agents - chemistry ; Anti-Inflammatory Agents - pharmacology ; Antioxidants - chemistry ; Antioxidants - pharmacology ; Bioactive Constituents, Metabolites, and Functions ; Cyclooxygenase 2 - genetics ; Cyclooxygenase 2 - immunology ; Inonotus - chemistry ; Inonotus - growth & development ; Macrophages - drug effects ; Macrophages - immunology ; Mass Spectrometry ; Mice ; Neurites - drug effects ; Neurites - immunology ; NF-kappa B - genetics ; NF-kappa B - immunology ; Nitric Oxide Synthase Type II - genetics ; Nitric Oxide Synthase Type II - immunology ; PC12 Cells ; Phenols - chemistry ; Phenols - pharmacology ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Rats ; RAW 264.7 Cells ; Steroids - chemistry ; Steroids - pharmacology</subject><ispartof>Journal of agricultural and food chemistry, 2021-01, Vol.69 (2), p.668-675</ispartof><rights>2021 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a336t-8fbea09088ab4821323665dc580023114df24e6e6e3ac7fe74bc92662ef661fc3</citedby><cites>FETCH-LOGICAL-a336t-8fbea09088ab4821323665dc580023114df24e6e6e3ac7fe74bc92662ef661fc3</cites><orcidid>0000-0003-4801-6514 ; 0000-0001-7969-9149</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33398984$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kou, Rong-Wei</creatorcontrib><creatorcontrib>Du, Shuang-Tian</creatorcontrib><creatorcontrib>Xia, Bing</creatorcontrib><creatorcontrib>Zhang, Qiang</creatorcontrib><creatorcontrib>Yin, Xia</creatorcontrib><creatorcontrib>Gao, Jin-Ming</creatorcontrib><title>Phenolic and Steroidal Metabolites from the Cultivated Edible Inonotus hispidus Mushroom and Their Bioactivities</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>A chemical study on the fruiting bodies of cultivated edible mushroom Inonotus hispidus resulted in 14 metabolites including three new hispolon congeners, named inonophenols A–B and one new lanostane triterpenoid, named inonoterpene A. These structures were identified by NMR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and electronic circular dichroism (ECD) data analysis. All metabolites were assessed for neurotrophic, anti-inflammatory, and antioxidative activities. Among them, inonophenols B and C were the most active in promoting PC-12 cell neurite outgrowth at a concentration of 10 μM. The phenolic derivatives reduced NO generation by lipopolysaccharide (LPS)-induced BV-2 microglial cells by suppressing the expression of toll-like receptor-4 (TLR-4) and the nuclear factor-kappa-B (NF-κB) signaling pathway as well as the inflammatory mediators including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Moreover, the phenolics showed antioxidant effects in DPPH scavenging assay with the IC50 values of 9.82–21.43 μM. These findings showed that I. hispidus may be a new source of neurotrophic and protective agents against neurodegenerative disorders.</description><subject>Animals</subject><subject>Anti-Inflammatory Agents - chemistry</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Antioxidants - chemistry</subject><subject>Antioxidants - pharmacology</subject><subject>Bioactive Constituents, Metabolites, and Functions</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - immunology</subject><subject>Inonotus - chemistry</subject><subject>Inonotus - growth & development</subject><subject>Macrophages - drug effects</subject><subject>Macrophages - immunology</subject><subject>Mass Spectrometry</subject><subject>Mice</subject><subject>Neurites - drug effects</subject><subject>Neurites - immunology</subject><subject>NF-kappa B - genetics</subject><subject>NF-kappa B - immunology</subject><subject>Nitric Oxide Synthase Type II - genetics</subject><subject>Nitric Oxide Synthase Type II - immunology</subject><subject>PC12 Cells</subject><subject>Phenols - chemistry</subject><subject>Phenols - pharmacology</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Rats</subject><subject>RAW 264.7 Cells</subject><subject>Steroids - chemistry</subject><subject>Steroids - pharmacology</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLxDAURoMozvjYu5IsXdgxjzZNlzqMD1AU1HVJ0xuaodOMSSr47804ozu5i1zC-T64B6EzSmaUMHqldJgtldEzoomQjO2hKS0YyQpK5T6aksRkshB0go5CWBJCZFGSQzThnFeykvkUrV86GFxvNVZDi18jeGdb1eMniKpJ_xECNt6tcOwAz8c-2k8VocWL1jY94IfBDS6OAXc2rG2blqcxdN6lwKbvrQPr8Y11SqegjRbCCTowqg9wunuP0fvt4m1-nz0-3z3Mrx8zxbmImTQNKFIRKVWTS0Y540IUrS5kOopTmreG5SDScKVLA2Xe6IoJwcAIQY3mx-hi27v27mOEEOuVDRr6Xg3gxlCzvCx4lRclSyjZotq7EDyYeu3tSvmvmpJ647lOnuuN53rnOUXOd-1js4L2L_ArNgGXW-An6kY_pGP_7_sGChyKvw</recordid><startdate>20210120</startdate><enddate>20210120</enddate><creator>Kou, Rong-Wei</creator><creator>Du, Shuang-Tian</creator><creator>Xia, Bing</creator><creator>Zhang, Qiang</creator><creator>Yin, Xia</creator><creator>Gao, Jin-Ming</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4801-6514</orcidid><orcidid>https://orcid.org/0000-0001-7969-9149</orcidid></search><sort><creationdate>20210120</creationdate><title>Phenolic and Steroidal Metabolites from the Cultivated Edible Inonotus hispidus Mushroom and Their Bioactivities</title><author>Kou, Rong-Wei ; Du, Shuang-Tian ; Xia, Bing ; Zhang, Qiang ; Yin, Xia ; Gao, Jin-Ming</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a336t-8fbea09088ab4821323665dc580023114df24e6e6e3ac7fe74bc92662ef661fc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Anti-Inflammatory Agents - chemistry</topic><topic>Anti-Inflammatory Agents - pharmacology</topic><topic>Antioxidants - chemistry</topic><topic>Antioxidants - pharmacology</topic><topic>Bioactive Constituents, Metabolites, and Functions</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - immunology</topic><topic>Inonotus - chemistry</topic><topic>Inonotus - growth & development</topic><topic>Macrophages - drug effects</topic><topic>Macrophages - immunology</topic><topic>Mass Spectrometry</topic><topic>Mice</topic><topic>Neurites - drug effects</topic><topic>Neurites - immunology</topic><topic>NF-kappa B - genetics</topic><topic>NF-kappa B - immunology</topic><topic>Nitric Oxide Synthase Type II - genetics</topic><topic>Nitric Oxide Synthase Type II - immunology</topic><topic>PC12 Cells</topic><topic>Phenols - chemistry</topic><topic>Phenols - pharmacology</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Rats</topic><topic>RAW 264.7 Cells</topic><topic>Steroids - chemistry</topic><topic>Steroids - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kou, Rong-Wei</creatorcontrib><creatorcontrib>Du, Shuang-Tian</creatorcontrib><creatorcontrib>Xia, Bing</creatorcontrib><creatorcontrib>Zhang, Qiang</creatorcontrib><creatorcontrib>Yin, Xia</creatorcontrib><creatorcontrib>Gao, Jin-Ming</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kou, Rong-Wei</au><au>Du, Shuang-Tian</au><au>Xia, Bing</au><au>Zhang, Qiang</au><au>Yin, Xia</au><au>Gao, Jin-Ming</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Phenolic and Steroidal Metabolites from the Cultivated Edible Inonotus hispidus Mushroom and Their Bioactivities</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2021-01-20</date><risdate>2021</risdate><volume>69</volume><issue>2</issue><spage>668</spage><epage>675</epage><pages>668-675</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>A chemical study on the fruiting bodies of cultivated edible mushroom Inonotus hispidus resulted in 14 metabolites including three new hispolon congeners, named inonophenols A–B and one new lanostane triterpenoid, named inonoterpene A. These structures were identified by NMR, high-resolution electrospray ionization mass spectrometry (HRESIMS), and electronic circular dichroism (ECD) data analysis. All metabolites were assessed for neurotrophic, anti-inflammatory, and antioxidative activities. Among them, inonophenols B and C were the most active in promoting PC-12 cell neurite outgrowth at a concentration of 10 μM. The phenolic derivatives reduced NO generation by lipopolysaccharide (LPS)-induced BV-2 microglial cells by suppressing the expression of toll-like receptor-4 (TLR-4) and the nuclear factor-kappa-B (NF-κB) signaling pathway as well as the inflammatory mediators including inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2). Moreover, the phenolics showed antioxidant effects in DPPH scavenging assay with the IC50 values of 9.82–21.43 μM. These findings showed that I. hispidus may be a new source of neurotrophic and protective agents against neurodegenerative disorders.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>33398984</pmid><doi>10.1021/acs.jafc.0c06822</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4801-6514</orcidid><orcidid>https://orcid.org/0000-0001-7969-9149</orcidid></addata></record> |
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subjects | Animals Anti-Inflammatory Agents - chemistry Anti-Inflammatory Agents - pharmacology Antioxidants - chemistry Antioxidants - pharmacology Bioactive Constituents, Metabolites, and Functions Cyclooxygenase 2 - genetics Cyclooxygenase 2 - immunology Inonotus - chemistry Inonotus - growth & development Macrophages - drug effects Macrophages - immunology Mass Spectrometry Mice Neurites - drug effects Neurites - immunology NF-kappa B - genetics NF-kappa B - immunology Nitric Oxide Synthase Type II - genetics Nitric Oxide Synthase Type II - immunology PC12 Cells Phenols - chemistry Phenols - pharmacology Plant Extracts - chemistry Plant Extracts - pharmacology Rats RAW 264.7 Cells Steroids - chemistry Steroids - pharmacology |
title | Phenolic and Steroidal Metabolites from the Cultivated Edible Inonotus hispidus Mushroom and Their Bioactivities |
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