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Comparative analysis of fat and muscle proteins in fenofibrate-fed type II diabetic OLETF rats: the fenofibrate-dependent expression of PEBP or C11orf59 protein

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dc.contributor.authorHahm, Jong Ryeal-
dc.contributor.authorAhn, Jin Sook-
dc.contributor.authorNoh, Hae Sook-
dc.contributor.authorBaek, Seon Mi-
dc.contributor.authorHa, Ji Hye-
dc.contributor.authorJung, Tae Sik-
dc.contributor.authorAn, Yong Jun-
dc.contributor.authorKim, Duk Kyu-
dc.contributor.authorKim, Deok Ryong-
dc.date.accessioned2025-04-01T06:30:44Z-
dc.date.available2025-04-01T06:30:44Z-
dc.date.issued2010-05-
dc.identifier.issn1976-6696-
dc.identifier.issn1976-670X-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/77636-
dc.description.abstractFenofibrate, an agonist of PPAR alpha, plays an important role in activating many proteins catalyzing lipid metabolism, and it also has a considerable effect on improvement of insulin sensitivity in the diabetic condition. To investigate fenofibrate-dependent expression of peripheral tissue proteins in diabetes, we analyzed whole muscle or fat proteins of fenofibrate-fed OLETF rats, an animal model of type II diabetes, using 2-dimensional gel electrophoresis. We found that many proteins were specifically expressed in a fenofibrate-dependent manner in these diabetic rats. In particular, a functionally unknown C11orf59 protein was differentially expressed in the muscle tissues (about 5-fold increase) in fenofibrate-fed OLETF rats as compared to control rats. Additionally, the signal proteins phosphatidylethanolamine binding protein and IkB interacting protein were differentially regulated in the fenofibrate-treated adipose tissues. We suggest here that these proteins might be involved in controlling lipid or carbohydrate metabolism in diabetes via PPARa activation. [BMB reports 2010; 43(5): 337-343]-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisher생화학분자생물학회-
dc.titleComparative analysis of fat and muscle proteins in fenofibrate-fed type II diabetic OLETF rats: the fenofibrate-dependent expression of PEBP or C11orf59 protein-
dc.typeArticle-
dc.publisher.location대한민국-
dc.identifier.doi10.5483/BMBRep.2010.43.5.337-
dc.identifier.scopusid2-s2.0-77953507944-
dc.identifier.wosid000278244700006-
dc.identifier.bibliographicCitationBMB Reports, v.43, no.5, pp 337 - 343-
dc.citation.titleBMB Reports-
dc.citation.volume43-
dc.citation.number5-
dc.citation.startPage337-
dc.citation.endPage343-
dc.type.docTypeArticle-
dc.identifier.kciidART001445628-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.subject.keywordPlusIMPROVES INSULIN SENSITIVITY-
dc.subject.keywordPlusRECEPTOR (PPAR)-ALPHA ACTIVATION-
dc.subject.keywordPlusPPAR-GAMMA ACTIVATION-
dc.subject.keywordPlusSKELETAL-MUSCLE-
dc.subject.keywordPlusADIPOSE-TISSUE-
dc.subject.keywordPlusKAPPA-B-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusLIVER-
dc.subject.keywordPlusMICE-
dc.subject.keywordPlusROSIGLITAZONE-
dc.subject.keywordAuthorC11orf59-
dc.subject.keywordAuthorFenofibrate-
dc.subject.keywordAuthorOLETF rats-
dc.subject.keywordAuthorPEBP-
dc.subject.keywordAuthorPPAR alpha-
dc.subject.keywordAuthorProteomics-
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