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Induction of heme oxygenase-1 protects against podocyte apoptosis under diabetic conditions

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dc.contributor.authorLee, Sang Choel-
dc.contributor.authorHan, Seung Hyeok-
dc.contributor.authorLi, Jin Ji-
dc.contributor.authorLee, Sun Ha-
dc.contributor.authorJung, Dong-Sub-
dc.contributor.authorKwak, Seung-Jae-
dc.contributor.authorKim, Seung Hye-
dc.contributor.authorKim, Dong Ki-
dc.contributor.authorYoo, Tae-Hyun-
dc.contributor.authorKim, Jin Hyun-
dc.contributor.authorChang, Se-Ho-
dc.contributor.authorHan, Dae Suk-
dc.contributor.authorKang, Shin-Wook-
dc.date.accessioned2022-12-27T05:06:52Z-
dc.date.available2022-12-27T05:06:52Z-
dc.date.issued2009-10-
dc.identifier.issn0085-2538-
dc.identifier.issn1523-1755-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/26150-
dc.description.abstractHeme oxygenase-1 (HO-1) is an anti-oxidant enzyme normally upregulated in response to oxidant injury. Here we determined the role of HO-1 in podocyte apoptosis in glomeruli of streptozotocin-treated rats and in immortalized mouse podocytes cultured in media containing normal or high glucose. HO-1 expression, its activity, the ratio of Bax/Bcl-2 protein, and active caspase-3 fragments were all significantly higher in isolated glomeruli of diabetic rats and in high glucose-treated podocytes. These increases were inhibited by zinc protoporphyrin treatment of the rats or by HO-1 siRNA treatment of the podocytes in culture. The number of apoptotic cells was also significantly increased in the glomeruli of diabetic rats and in high glucose-treated podocytes. Inhibition of HO-1 accentuated the increase in apoptotic cells both in vivo and in vitro. Our findings suggest that HO-1 expression protects against podocyte apoptosis under diabetic conditions. Kidney International (2009) 76, 838-848; doi:10.1038/ki.2009.286; published online 5 August 2009-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE INC-
dc.titleInduction of heme oxygenase-1 protects against podocyte apoptosis under diabetic conditions-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1038/ki.2009.286-
dc.identifier.scopusid2-s2.0-70349686948-
dc.identifier.wosid000270354700012-
dc.identifier.bibliographicCitationKIDNEY INTERNATIONAL, v.76, no.8, pp 838 - 848-
dc.citation.titleKIDNEY INTERNATIONAL-
dc.citation.volume76-
dc.citation.number8-
dc.citation.startPage838-
dc.citation.endPage848-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaUrology & Nephrology-
dc.relation.journalWebOfScienceCategoryUrology & Nephrology-
dc.subject.keywordPlusRENAL INJURY-
dc.subject.keywordPlusDIFFERENTIAL EXPRESSION-
dc.subject.keywordPlusOXIDATIVE STRESS-
dc.subject.keywordPlusMESSENGER-RNA-
dc.subject.keywordPlusGROWTH-FACTOR-
dc.subject.keywordPlusKIDNEY-
dc.subject.keywordPlusGENE-
dc.subject.keywordPlusISCHEMIA-
dc.subject.keywordPlusREPERFUSION-
dc.subject.keywordPlusPATHWAYS-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthordiabetic nephropathy-
dc.subject.keywordAuthorheme oxygenase-1-
dc.subject.keywordAuthorhigh glucose-
dc.subject.keywordAuthorpodocyte-
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