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The Protective Effect of Quercetin-3-O-beta -D-Glucuronopyranoside on Ethanol-induced Damage in Cultured Feline Esophageal Epithelial Cells

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dc.contributor.authorCho, Jung Hyun-
dc.contributor.authorPark, Sun Young-
dc.contributor.authorLee, Ho Sung-
dc.contributor.authorWhang, Wan Kyunn-
dc.contributor.authorSohn, Uy Dong-
dc.date.available2019-05-29T09:39:35Z-
dc.date.issued2011-12-
dc.identifier.issn1226-4512-
dc.identifier.issn2093-3827-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21074-
dc.description.abstractQuercetin-3-O-beta -D-glucuronopyranoside (QGC) is a flavonoid glucoside extracted from Rumex Aquaticus Herba. We aimed to explore its protective effect against ethanol-induced cell damage and the mechanism involved in the effect in feline esophageal epithelial cells (EEC). Cell viability was tested and 2',7'-dichlorofluorescin diacetate assay was used to detect intracellular H2O2 production. Western blotting analysis was performed to investigate MAPK activation and interleukin 6 (IL-6) expression. Exposure of cells to 10% ethanol time-dependently decreased cell viability. Notably, exposure to ethanol for 30 min decreased cell viability to 43.4%. When cells were incubated with 50 mu M QGC for 12 h prior to and during ethanol treatment, cell viability was increased to 65%. QGC also inhibited the H2O2 production and activation of ERK 1/2 induced by ethanol. Pretreatment of cells with the NADPH oxidase inhibitor, diphenylene iodonium, also inhibited the ethanol-induced ERK 1/2 activation. Treatment of cells with ethanol for 30 or 60 min in the absence or presence of QGC exhibited no changes in the IL-6 expression or release compared to control. Taken together, the data indicate that the cytoprotective effect of QGC against ethanol-induced cell damage may involve inhibition of ROS generation and downstream activation of the ERK 1/2 in feline EEC.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.titleThe Protective Effect of Quercetin-3-O-beta -D-Glucuronopyranoside on Ethanol-induced Damage in Cultured Feline Esophageal Epithelial Cells-
dc.typeArticle-
dc.identifier.doi10.4196/kjpp.2011.15.6.319-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY, v.15, no.6, pp 319 - 326-
dc.identifier.kciidART001617927-
dc.description.isOpenAccessN-
dc.identifier.wosid000298905800001-
dc.identifier.scopusid2-s2.0-84862914361-
dc.citation.endPage326-
dc.citation.number6-
dc.citation.startPage319-
dc.citation.titleKOREAN JOURNAL OF PHYSIOLOGY & PHARMACOLOGY-
dc.citation.volume15-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorFlavonoid-
dc.subject.keywordAuthorHydrogen peroxide-
dc.subject.keywordAuthorERK-
dc.subject.keywordAuthorEsophageal epithelial cell-
dc.subject.keywordAuthorEthanol-
dc.subject.keywordPlusOXYGEN SPECIES PRODUCTION-
dc.subject.keywordPlusACTIVATED PROTEIN-KINASE-
dc.subject.keywordPlusALCOHOL-RELATED DISEASES-
dc.subject.keywordPlusREACTIVE OXYGEN-
dc.subject.keywordPlusHEME OXYGENASE-1-
dc.subject.keywordPlusMAP KINASE-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusINDUCED CYTOTOXICITY-
dc.subject.keywordPlusANTIOXIDANT ACTIVITY-
dc.subject.keywordPlusCYTOKINE PRODUCTION-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaPhysiology-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryPhysiology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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