Amomum xanthoides extract prevents cytokine-induced cell death of RINm5F cells through the inhibition of nitric oxide formation

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dc.contributor.authorKwon, KBko
dc.contributor.authorKim, JHko
dc.contributor.authorLee, YRko
dc.contributor.authorLee, HYko
dc.contributor.authorJeong, YJko
dc.contributor.authorRho, HWko
dc.contributor.authorRyu, DGko
dc.contributor.authorPark, JWko
dc.contributor.authorPark, BHko
dc.date.accessioned2024-03-22T03:01:42Z-
dc.date.available2024-03-22T03:01:42Z-
dc.date.created2024-03-21-
dc.date.created2024-03-21-
dc.date.issued2003-05-
dc.identifier.citationLIFE SCIENCES, v.73, no.2, pp.181 - 191-
dc.identifier.issn0024-3205-
dc.identifier.urihttp://hdl.handle.net/10203/318672-
dc.description.abstractWe previously showed that Amomum xanthoides extract prevented alloxan-induced diabetes through the suppression of NF-kappaB activation. In this study, the preventive effects of A. xanthoides extract on cytokine-induced beta-cell destruction were examined. Cytokines produced by immune cells infiltrating pancreatic islets are important mediators of beta-cell destruction in insulin-dependent diabetes mellitus. A. xanthoides extract completely protected interleukin-1beta (IL-1beta) and interferon-gamma (IFN-gamma)-mediated cytotoxicity in rat insulinoma cell line (RINm5F). Incubation with A. xanthoides extract resulted in a significant reduction in IL-1beta and IFN-gamma-induced nitric oxide (NO) production, a finding that correlated well with reduced levels of the inducible form of NO synthase (iNOS) mRNA and protein. The molecular mechanism by which A. xanthoides extract inhibited iNOS gene expression appeared to involve the inhibition of NF-kappaB activation. Our results revealed the possible therapeutic value of A. xanthoides extract for the prevention of diabetes mellitus progression. (C) 2003 Elsevier Science Inc. All rights reserved.-
dc.languageEnglish-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleAmomum xanthoides extract prevents cytokine-induced cell death of RINm5F cells through the inhibition of nitric oxide formation-
dc.typeArticle-
dc.identifier.wosid000182909300005-
dc.identifier.scopusid2-s2.0-0037725422-
dc.type.rimsART-
dc.citation.volume73-
dc.citation.issue2-
dc.citation.beginningpage181-
dc.citation.endingpage191-
dc.citation.publicationnameLIFE SCIENCES-
dc.identifier.doi10.1016/S0024-3205(03)00267-4-
dc.contributor.localauthorPark, BH-
dc.contributor.nonIdAuthorKwon, KB-
dc.contributor.nonIdAuthorKim, JH-
dc.contributor.nonIdAuthorLee, YR-
dc.contributor.nonIdAuthorLee, HY-
dc.contributor.nonIdAuthorJeong, YJ-
dc.contributor.nonIdAuthorRho, HW-
dc.contributor.nonIdAuthorRyu, DG-
dc.contributor.nonIdAuthorPark, JW-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordAuthorAntomum xanthoides extract-
dc.subject.keywordAuthornitric oxide-
dc.subject.keywordAuthorRIN cells-
dc.subject.keywordAuthorcytokine-
dc.subject.keywordPlusNF-KAPPA-B-
dc.subject.keywordPlusDEPENDENT DIABETES-MELLITUS-
dc.subject.keywordPlusVIBRIO-VULNIFICUS CYTOLYSIN-
dc.subject.keywordPlusBETA-CELL-
dc.subject.keywordPlusSYNTHASE EXPRESSION-
dc.subject.keywordPlusANTIOXIDANT ENZYMES-
dc.subject.keywordPlusPANCREATIC-ISLETS-
dc.subject.keywordPlusINSULIN-SECRETION-
dc.subject.keywordPlusFREE-RADICALS-
dc.subject.keywordPlusRAT-
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