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Amelioration of High-Insulin-Induced Skeletal Muscle Cell Insulin Resistance by Resveratrol Is Linked to Activation of AMPK and Restoration of GLUT4 Translocation

机译:通过白藜芦醇改善高胰岛素诱导的骨骼肌细胞胰岛素耐药性与AMPK的激活和Glut4易位的恢复有关

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摘要

Insulin resistance, the hallmark of type 2 diabetes mellitus (T2DM), is linked to hyperinsulinemia, which develops to counterbalance initial peripheral hormone resistance. Studies indicate that chronically elevated levels of insulin lead to skeletal muscle insulin resistance by deregulating steps within the insulin signaling cascade. The polyphenol resveratrol (RSV) has been shown to have antidiabetic properties in vitro and in vivo. In the present study, we examined the effect of RSV on high insulin (HI)-induced insulin resistance in skeletal muscle cells in vitro and investigated the mechanisms involved. Parental and GLUT4myc-overexpressing L6 rat skeletal muscle cells were used. [3H]2-deoxyglucose (2DG) uptake was measured, and total and phosphorylated levels of specific proteins were examined by immunoblotting. Exposure of L6 cells to HI levels (100 nM) for 24 h decreased the acute-insulin-stimulated 2DG uptake, indicating insulin resistance. HI increased ser307 and ser636/639 phosphorylation of IRS-1 (to 184% ± 12% and 225% ± 28.9% of control, with p < 0.001 and p < 0.01, respectively) and increased the phosphorylation levels of mTOR (174% ± 6.7% of control, p < 0.01) and p70 S6K (228% ± 33.5% of control, p < 0.01). Treatment with RSV abolished these HI-induced responses. Furthermore, RSV increased the activation of AMPK and restored the insulin-mediated increase in plasma membrane GLUT4 glucose transporter levels. These data suggest that RSV has a potential to counteract the HI-induced muscle insulin resistance.
机译:胰岛素抵抗,2型糖尿病(T2DM)的标志与高胰岛素血症联系,其发展以抵抗初始外周激素抗性。研究表明,通过胰岛素信号传导级联的放松步骤,慢性升高的胰岛素水平导致骨骼肌胰岛素抵抗。多酚白藜芦醇(RSV)已被证明在体外和体内具有抗糖尿病性能。在本研究中,我们研究了RSV对高胰岛素(HI)诱导的胰岛素抵抗体外胰岛素抗性的影响,并研究了所涉及的机制。使用父母和Glut4MYC过表达L6大鼠骨骼肌细胞。测量2-脱氧葡萄糖(2Dg)摄取,通过免疫印迹检查总和磷酸化水平的特异性蛋白质。将L6细胞暴露于HI水平(100nm)24小时降低急性胰岛素刺激的2Dg摄取,表明胰岛素抗性。 HI增加SER307和SER636 / 639 IRS-1的磷酸化(分别为P <0.001和P <0.01的控制(分别为184%±12%和225%±28.9%)并增加MTOR的磷酸化水平(174%± 6.7%的控制,P <0.01)和P70 S6K(对照的228%±33.5%,P <0.01)。用RSV治疗废除了这些高诱导的反应。此外,RSV增加了AMPK的激活并恢复了胰岛素介导的血浆膜GLUT4葡萄糖转运蛋白水平的增加。这些数据表明RSV有可能抵消Hi诱导的肌肉胰岛素抵抗力。

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