来自:中国糖尿病资讯网 编辑:editor|点击数:|2012-03-06
·糖尿病基础研究·
牛燕媚 刘彦辉 李慧阁 苏照鹏 傅力
基金项目:国家自然科学基金资助项目(30871213);天津市应用基础及前沿技术重点研究计划(09JCZDJC17400)。
作者单位: 300070天津,天津医科大学康复与运动医学系 (牛燕媚、傅力);天津市运动生理与运动医学重点实验室 (刘彦辉、李慧阁、苏照鹏)
【摘要】目的探讨胰岛素受体底物蛋白1 (IRS1)及其丝氨酸磷酸化在胰岛素抵抗(IR)发生中的作用。方法C57BL/6小鼠40只随机分为正常饮食组(NC组)和高脂饮食组(HF组),HC组喂养高脂饮食16周后建立IR模型。16周后处死,检测空腹血清胰岛素和口服糖耐量; RT-PCR检测小鼠骨骼肌TSC2和IRS1 mRNA表达。Western blot和免疫荧光染色检测骨骼肌TSC2、IRS1、IRS1Ser307和 IRS1Ser636/639蛋白表达。结果与NF组相比,HC组小鼠空腹血清胰岛素显著升高(P<0.01),糖耐量显著受损,骨骼肌细胞TSC2 mRNA和蛋白均显著降低(P<0.05), HF组 pIRS1Ser307 和pIRS1Ser636/639蛋白表达显著增加(P<0.01)。结论高脂饮食可能通过抑制TSC2基因和蛋白表达,增强 IRS1Ser307和IRS1Ser636/639的磷酸化水平,阻碍胰岛素信号传导,诱发IR。
【关键词】胰岛素抵抗;TSC2;胰岛素受体底物蛋白1;IRS1Ser307;IRS1Ser636/639
doi:10.3969/j.issn.1006-6187.2012.02.015
The study of the role of IRS1 and its serine phosphorylation activity in pathogenesis of insulin resistanceNIU Yan-mei, LIU Yan-hui, LI Hui-ge, et al.Department of Rehabilitation and Sports Medicine, Tianjin Medical University, Tianjin 300070, China
【Abstract】ObjectiveTo investigate the effects of insulin receptor substrate 1 (IRS1) and activity of IRS1 serine phosphorylation on the development of insulin resistant. Methods20 male C57BL/6 mice were divided into normal diet group (NC) and high fat diet group (HF) and all mice showed insulin resistance. The mice in HF were fed with high fat diet for 16 weeks. Serum insulin concentration was also evaluated by ELISA. RT-PCR, Western blot and immunofluorescence were performed to detect TSC2 and IRS1 mRNA and protein expression in skeletal muscle. ResultsAs compared with NC group, HF group showed that fasting insulin value was increased (P<0.01), OGTT was damaged, mRNA and protein expressions of TSC2 of skeletal muscle of mice were decreased (P<0.05), and the expression of pIRS1Ser307 and pIRS1Ser636/639 was increased (P<0.01).ConclusionsHigh-fat diet possibly produces IR by inhibiting TSC2 mRNA and protein expression, and by increasing IRS1Ser307 and IRS1Ser636/639 phosphorylation levels in mice skeletal muscle.
【Key words】Insulin resistance; TSC2; IRS1; IRS1Ser307; IRS1Ser636/639
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