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Streptozotocin-induced diabetes increases the interaction of Bad/BCl-X-L and decreases the binding of pBad/14-3-3 in rat testis

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dc.contributor.authorKoh, Phil-Ok-
dc.date.accessioned2022-12-27T06:52:50Z-
dc.date.available2022-12-27T06:52:50Z-
dc.date.issued2007-09-08-
dc.identifier.issn0024-3205-
dc.identifier.issn1879-0631-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/28284-
dc.description.abstractSexual dysfunction is frequently associated with diabetes in males. The present study was designed to evaluate whether streptozotocin-induced diabetes increases apoptotic cell death in rat testis through the regulation of Bcl-2 family proteins. Diabetes was induced by a single intravenous injection of streptozotocin (40 mg/kg body weight) and testis samples were collected after 3 months. The number of positive cells for TUNEL histochemistry was significantly increased in the testicular germ cells of the diabetic group, compared to those of control. The levels of Bcl-2 and Bcl-X-L, anti-apoptotic proteins, were decreased in the diabetic group. In contrast, the levels of Bax and Bad, pro-apoptotic factors, were increased in the diabetic group, compared with the control group. Moreover, the diabetic condition increased the interaction of Bad and Bcl-X-L, and decreased the binding of pBad and 14-3-3. 14-3-3 acts as an anti-apoptotic factor through interaction with Bad. Our findings suggest that streptozotocin-induced diabetes increases apoptotic cell death in testis tissue through the up-and down-regulation of Bcl-2 family proteins and the interaction of Bad and Bcl-X-L. (C)2007 Elsevier Inc. All rights reserved.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherPERGAMON-ELSEVIER SCIENCE LTD-
dc.titleStreptozotocin-induced diabetes increases the interaction of Bad/BCl-X-L and decreases the binding of pBad/14-3-3 in rat testis-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.lfs.2007.08.017-
dc.identifier.wosid000250188500007-
dc.identifier.bibliographicCitationLIFE SCIENCES, v.81, no.13, pp 1079 - 1084-
dc.citation.titleLIFE SCIENCES-
dc.citation.volume81-
dc.citation.number13-
dc.citation.startPage1079-
dc.citation.endPage1084-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusCELL-DEATH-
dc.subject.keywordPlusINDUCED HYPERGLYCEMIA-
dc.subject.keywordPlusBCL-2-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusBAX-
dc.subject.keywordPlusPROTEIN-
dc.subject.keywordPlusHETERODIMERIZES-
dc.subject.keywordPlusDYSFUNCTION-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusPREVENTION-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthorBcl-2 family protein-
dc.subject.keywordAuthorrat testis-
dc.subject.keywordAuthorstreptozotocin-induced diabetes-
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