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Cited 13 time in webofscience Cited 14 time in scopus
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Antigastritis effects of Armillariella tabescens (Scop.) Sing. and the identification of its anti-inflammatory metabolites

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dc.contributor.authorLee, Seulah-
dc.contributor.authorLee, Dahae-
dc.contributor.authorPark, Jun Yeon-
dc.contributor.authorSeok, Soonja-
dc.contributor.authorJang, Tae Su-
dc.contributor.authorPark, Hyun Bong-
dc.contributor.authorShim, Sang Hee-
dc.contributor.authorKang, Ki Sung-
dc.contributor.authorKim, Ki Hyun-
dc.date.available2020-02-27T11:42:03Z-
dc.date.created2020-02-06-
dc.date.issued2018-03-
dc.identifier.issn0022-3573-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4022-
dc.description.abstractObjectivesThis study demonstrates the biological and chemical analysis of the mushroom Armillariella tabescens (Scop.) Sing. (Tricholomataceae). MethodsChemical structures of the isolates were determined by 1D and 2D NMR, and ESI-MS, as well as comparison with previously reported data. All isolates were tested for anti-inflammatory effects based on their ability to inhibit LPS-stimulated nitric oxide (NO) production in RAW264.7 cells. Key findingsWe found that the MeOH extract of the fruiting bodies of A. tabescens showed antigastritis activity against ethanol-induced gastric damage in rats and notably reduced the gastric damage index compared to control in a concentration-dependent manner. Chemical investigation of the MeOH extract led to the isolation of four steroids (1-4), three alkaloids (5-7), two nucleic acids (8-9) and four fatty acids (10-13). This is the first study to report the identification of all isolates, except for compound 7, from A. tabescens. Compounds 1, 2, 3, 4 and 10 showed inhibition on LPS-stimulated NO production. Treatment with compound 10 inhibited expression of iNOS, COX-2, phospho-IKK, IKK, phospho-IB, IB and NF-kappa B in LPS-stimulated RAW264.7 cells. ConclusionsCompound 10 likely contributes to the health benefits of A. tabescens as an antigastritis agent through its anti-inflammatory effects.-
dc.language영어-
dc.language.isoen-
dc.publisherWILEY-
dc.relation.isPartOfJOURNAL OF PHARMACY AND PHARMACOLOGY-
dc.subjectNITRIC-OXIDE PRODUCTION-
dc.subjectTOLL-LIKE RECEPTOR-4-
dc.subjectKAPPA-B ACTIVATION-
dc.subjectFRUITING BODIES-
dc.subjectINFLAMMATORY RESPONSES-
dc.subjectCHEMICAL-CONSTITUENTS-
dc.subjectSIGNAL-TRANSDUCTION-
dc.subjectINHIBITORY-ACTIVITY-
dc.subjectHERICIUM-ERINACEUS-
dc.subjectRAW264.7 CELLS-
dc.titleAntigastritis effects of Armillariella tabescens (Scop.) Sing. and the identification of its anti-inflammatory metabolites-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000425094800011-
dc.identifier.doi10.1111/jphp.12871-
dc.identifier.bibliographicCitationJOURNAL OF PHARMACY AND PHARMACOLOGY, v.70, no.3, pp.404 - 412-
dc.identifier.scopusid2-s2.0-85042124320-
dc.citation.endPage412-
dc.citation.startPage404-
dc.citation.titleJOURNAL OF PHARMACY AND PHARMACOLOGY-
dc.citation.volume70-
dc.citation.number3-
dc.contributor.affiliatedAuthorLee, Dahae-
dc.contributor.affiliatedAuthorPark, Jun Yeon-
dc.contributor.affiliatedAuthorKang, Ki Sung-
dc.type.docTypeArticle-
dc.subject.keywordAuthorantigastritis-
dc.subject.keywordAuthoranti-inflammation-
dc.subject.keywordAuthorArmillariella tabescens-
dc.subject.keywordAuthorNF-kappa B-
dc.subject.keywordAuthorTricholomataceae-
dc.subject.keywordPlusNITRIC-OXIDE PRODUCTION-
dc.subject.keywordPlusTOLL-LIKE RECEPTOR-4-
dc.subject.keywordPlusKAPPA-B ACTIVATION-
dc.subject.keywordPlusFRUITING BODIES-
dc.subject.keywordPlusINFLAMMATORY RESPONSES-
dc.subject.keywordPlusCHEMICAL-CONSTITUENTS-
dc.subject.keywordPlusSIGNAL-TRANSDUCTION-
dc.subject.keywordPlusINHIBITORY-ACTIVITY-
dc.subject.keywordPlusHERICIUM-ERINACEUS-
dc.subject.keywordPlusRAW264.7 CELLS-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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