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Glutathione Peroxidase 3 Mediates the Antioxidant Effect of Peroxisome Proliferator-Activated Receptor gamma in Human Skeletal Muscle Cells

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dc.contributor.authorChung, Sung Soo-
dc.contributor.authorKim, Min-
dc.contributor.authorYoun, Byoung-Soo-
dc.contributor.authorLee, Nam Seok-
dc.contributor.authorLee, In Kyu-
dc.contributor.authorKim, Jae Bum-
dc.contributor.authorLee, Hong Kyu-
dc.contributor.authorPark, Kyong Soo-
dc.contributor.authorCho, Young Min-
dc.contributor.authorLee, Yun Sok-
dc.contributor.authorPark, Ji Woo-
dc.date.accessioned2012-06-26T06:15:47Z-
dc.date.available2012-06-26T06:15:47Z-
dc.date.issued2009-01-01-
dc.identifier.citationMOLECULAR AND CELLULAR BIOLOGY; Vol.29 1; 20-30ko_KR
dc.identifier.issn0270-7306-
dc.identifier.urihttps://hdl.handle.net/10371/77452-
dc.description.abstractOxidative stress plays an important role in the pathogenesis of insulin resistance and type 2 diabetes mellitus and in diabetic vascular complications. Thiazolidinediones (TZDs), a class of peroxisome proliferator-activated receptor gamma (PPAR gamma) agonists, improve insulin sensitivity and are currently used for the treatment of type 2 diabetes mellitus. Here, we show that TZD prevents oxidative stress-induced insulin resistance in human skeletal muscle cells, as indicated by the increase in insulin-stimulated glucose uptake and insulin signaling. Importantly, TZD-mediated activation of PPAR gamma induces gene expression of glutathione peroxidase 3 (GPx3), which reduces extracellular H(2)O(2) levels causing insulin resistance in skeletal muscle cells. Inhibition of GPx3 expression prevents the antioxidant effects of TZDs on insulin action in oxidative stress-induced insulin-resistant cells, suggesting that GPx3 is required for the regulation of PPAR gamma-mediated antioxidant effects. Furthermore, reduced plasma GPx3 levels were found in patients with type 2 diabetes mellitus and in db/db/DIO mice. Collectively, these results suggest that the antioxidant effect of PPAR gamma is exclusively mediated by GPx3 and further imply that GPx3 may be a therapeutic target for insulin resistance and diabetes mellitus.ko_KR
dc.description.sponsorshipThis study was supported by 21C Frontier Functional Proteomics
Project from the Korean Ministry of Education, Science and Technology and MarineBio21, Ministry of Maritime Affairs and Fisheries,
South Korea.
ko_KR
dc.language.isoenko_KR
dc.publisherAMER SOC MICROBIOLOGYko_KR
dc.titleGlutathione Peroxidase 3 Mediates the Antioxidant Effect of Peroxisome Proliferator-Activated Receptor gamma in Human Skeletal Muscle Cellsko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor정성수-
dc.contributor.AlternativeAuthor김민-
dc.contributor.AlternativeAuthor윤병수-
dc.contributor.AlternativeAuthor이남석-
dc.contributor.AlternativeAuthor박지우-
dc.contributor.AlternativeAuthor이인규-
dc.contributor.AlternativeAuthor이윤속-
dc.contributor.AlternativeAuthor김재범-
dc.contributor.AlternativeAuthor조영민-
dc.contributor.AlternativeAuthor이홍규-
dc.contributor.AlternativeAuthor박경수-
dc.identifier.doi10.1128/MCB.00544-08-
dc.citation.journaltitleMOLECULAR AND CELLULAR BIOLOGY-
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