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Cited 11 time in webofscience Cited 11 time in scopus
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Protective effect of alpha-mangostin against iodixanol-induced apoptotic damage in LLC-PK1 cells

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dc.contributor.authorLee, Dahae-
dc.contributor.authorChoi, Young Ok-
dc.contributor.authorKim, Ki Hyun-
dc.contributor.authorChin, Young-Won-
dc.contributor.authorNamgung, Hojin-
dc.contributor.authorYamabe, Noriko-
dc.contributor.authorJung, Kiwon-
dc.date.available2020-02-28T00:45:37Z-
dc.date.created2020-02-07-
dc.date.issued2016-08-01-
dc.identifier.issn0960-894X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/8013-
dc.description.abstractRadiographic contrast media facilitate the visibility of internal body structures, but its use to patients with lowered renal function needs to be careful because of severe side effect in kidney. The present study aims to evaluate potential protective effect and mechanism of Alpha mangostin (alpha-mangostin) against contrast-induced apoptotic damage in LLC-PK1 cells. As a result, alpha-mangostin in non-toxic concentrations improved the viability of the iodixanol-treated cells up to 90.42% against contrast-induced damage in LLC-PK1 cells. Iodixanol treatment increased the phosphorylation of p38, ERK and cleavage of caspase-3 in LLC-PK1 cells, which were significantly decreased by co-treatment with alpha-mangostin (2.5 and 5 mu M). The protective effect of alpha-mangostin on contrast-induced apoptotic damage was mediated by the inhibition of MAPKs and caspase activation. (C) 2016 Elsevier Ltd. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.relation.isPartOfBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.subjectCONTRAST-INDUCED NEPHROPATHY-
dc.subjectN-ACETYLCYSTEINE-
dc.subjectCYCLE ARREST-
dc.subjectP38 MAPK-
dc.subjectIN-VIVO-
dc.subjectCANCER-
dc.subjectXANTHONES-
dc.subjectATTENUATION-
dc.subjectINHIBITION-
dc.subjectPREVENTION-
dc.titleProtective effect of alpha-mangostin against iodixanol-induced apoptotic damage in LLC-PK1 cells-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000380574100081-
dc.identifier.doi10.1016/j.bmcl.2016.05.031-
dc.identifier.bibliographicCitationBIOORGANIC & MEDICINAL CHEMISTRY LETTERS, v.26, no.15, pp.3806 - 3809-
dc.identifier.scopusid2-s2.0-84978832036-
dc.citation.endPage3809-
dc.citation.startPage3806-
dc.citation.titleBIOORGANIC & MEDICINAL CHEMISTRY LETTERS-
dc.citation.volume26-
dc.citation.number15-
dc.contributor.affiliatedAuthorLee, Dahae-
dc.contributor.affiliatedAuthorYamabe, Noriko-
dc.type.docTypeArticle-
dc.subject.keywordAuthorContrast-
dc.subject.keywordAuthorAlpha mangostin-
dc.subject.keywordAuthorIodixanol-
dc.subject.keywordAuthorMAPK-
dc.subject.keywordAuthorCaspase-
dc.subject.keywordPlusCONTRAST-INDUCED NEPHROPATHY-
dc.subject.keywordPlusN-ACETYLCYSTEINE-
dc.subject.keywordPlusCYCLE ARREST-
dc.subject.keywordPlusP38 MAPK-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCANCER-
dc.subject.keywordPlusXANTHONES-
dc.subject.keywordPlusATTENUATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusPREVENTION-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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