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

被引:143
作者
Chung, Sung Soo [1 ]
Kim, Min [1 ]
Youn, Byoung-Soo [2 ]
Lee, Nam Seok [2 ]
Park, Ji Woo [2 ]
Lee, In Kyu [3 ]
Lee, Yun Sok [4 ]
Kim, Jae Bum [4 ]
Cho, Young Min [1 ]
Lee, Hong Kyu [1 ]
Park, Kyong Soo [1 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul 110744, South Korea
[2] Korea Univ, Coll Life Sci & Biotechnol, AdipoGen Inc, Seoul, South Korea
[3] Kyungpook Natl Univ, Dept Internal Med, Taegu, South Korea
[4] Seoul Natl Univ, Dept Biol Sci, Res Ctr Funct Cellul, Seoul 151742, South Korea
关键词
INDUCED INSULIN-RESISTANCE; OXIDATIVE STRESS; MICROMOLAR CONCENTRATIONS; PPAR-GAMMA; PLASMA; EXPRESSION; GENE; DISEASE; ALPHA; HYDROPEROXIDE;
D O I
10.1128/MCB.00544-08
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Oxidative 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 H2O2 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.
引用
收藏
页码:20 / 30
页数:11
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