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Preconditioning with thyroid hormone (3,5,3-triiodothyronine) prevents renal ischemia-reperfusion injury in mice

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dc.contributor.authorKim, Suh Min-
dc.contributor.authorKim, Si-Wha-
dc.contributor.authorJung, Yoo-Jun-
dc.contributor.authorMin, Sang-Il-
dc.contributor.authorMin, Seung-Kee-
dc.contributor.authorKim, Sang Joon-
dc.contributor.authorHa, Jongwon-
dc.date.accessioned2024-01-09T14:32:39Z-
dc.date.available2024-01-09T14:32:39Z-
dc.date.issued2014-03-
dc.identifier.issn0039-6060-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/70448-
dc.description.abstractBackground. 3,5,3-triiodothyronine (T3) was found to decrease ischemia-reperfusion (I/R) injury of liver and myocardium in animal models when preconditioned 48 hours in advance of the I/R injury. The purpose of this study was to evaluate the effects of T3 preconditioning on renal I/R injury with different time intervals and to determine the changes in antioxidants, apoptosis, and nitric oxide synthase (NOS) in each condition. Methods. In male C57BL/6 mice, renal I/R injury was induced by temporary ligation of the bilateral renal pedicles for 45 minutes followed by a reperfusion period for 24 hours. Preconditioning with intraperitoneal injection of T3 was performed 24 or 6 hours before or at the time of I/R injury. Results. From the histologic examination, tubular injury was decreased in mice preconditioned with T3 6 hours before I/R injury. The levels of proinflammatory cytokines were decreased with T3 preconditioning, either 6 hours or at the time of I/R injury. The levels of glutathione were increased in all treatment groups. Expressions of neuronal NOS were increased when preconditioned 6 hours before or t the time of I/R injury. The number of apoptotic tubular epithelial cell evaluated by terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling assay was decreased when preconditioned immediately before I/R injury. Conclusion. Preconditioning with T3 6 hours or immediately before I/R injury had a protective effect on renal I/R injury. The changes of NOS and antiapoptosis, other than well-known antioxidative properties, may play a.role in the effect of short-term preconditioning.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherMOSBY-ELSEVIER-
dc.titlePreconditioning with thyroid hormone (3,5,3-triiodothyronine) prevents renal ischemia-reperfusion injury in mice-
dc.typeArticle-
dc.identifier.doi10.1016/j.surg.2013.10.005-
dc.identifier.bibliographicCitationSURGERY, v.155, no.3, pp 554 - 561-
dc.description.isOpenAccessN-
dc.identifier.wosid000331991200025-
dc.identifier.scopusid2-s2.0-84894025741-
dc.citation.endPage561-
dc.citation.number3-
dc.citation.startPage554-
dc.citation.titleSURGERY-
dc.citation.volume155-
dc.type.docTypeArticle-
dc.publisher.location미국-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordPlusISCHEMIA/REPERFUSION INJURY-
dc.subject.keywordPlusWARM ISCHEMIA-
dc.subject.keywordPlusNO-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusENDOTHELIUM-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPROTECTION-
dc.relation.journalResearchAreaSurgery-
dc.relation.journalWebOfScienceCategorySurgery-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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