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胰岛素对人骨骼肌和脂肪组织中基因表达的调控。2型糖尿病中特定缺陷的证据。

Regulation by insulin of gene expression in human skeletal muscle and adipose tissue. Evidence for specific defects in type 2 diabetes.

作者信息

Ducluzeau P H, Perretti N, Laville M, Andreelli F, Vega N, Riou J P, Vidal H

机构信息

Institut National de la Santé et de la Recherche Médicale INSERM U.449, Faculty of Medicine R. Laennec, Lyon, France.

出版信息

Diabetes. 2001 May;50(5):1134-42. doi: 10.2337/diabetes.50.5.1134.

Abstract

Defective regulation of gene expression may be involved in the pathogenesis of type 2 diabetes. We have characterized the concerted regulation by insulin (3-h hyperinsulinemic clamp) of the expression of 10 genes related to insulin action in skeletal muscle and in subcutaneous adipose tissue, and we have verified whether a defective regulation of some of them could be specifically encountered in tissues of type 2 diabetic patients. Basal mRNA levels (determined by reverse transcriptase-competitive polymerase chain reaction) of insulin receptor, insulin receptor substrate-1, p85alpha phosphatidylinositol 3-kinase (PI3K), p110alphaPI3K, p110betaPI3K, GLUT4, glycogen synthase, and sterol regulatory-element-binding protein-1c (SREBP-1c) were similar in muscle of control (n = 17), type 2 diabetic (n = 9), type 1 diabetic (n = 9), and nondiabetic obese (n = 9) subjects. In muscle, the expression of hexokinase II was decreased in type 2 diabetic patients (P < 0.01). In adipose tissue, SREBP-1c (P < 0.01) mRNA expression was reduced in obese (nondiabetic and type 2 diabetic) subjects and was negatively correlated with the BMI of the subjects (r = -0.63, P = 0.02). Insulin (+/-1,000 pmol/l) induced a two- to threefold increase (P < 0.05) in hexokinase II, p85alphaPI3K, and SREBP-1c mRNA levels in muscle and in adipose tissue in control subjects, in insulin-resistant nondiabetic obese patients, and in hyperglycemic type 1 diabetic subjects. Upregulation of these genes was completely blunted in type 2 diabetic patients. This study thus provides evidence for a specific defect in the regulation of a group of important genes in response to insulin in peripheral tissues of type 2 diabetic patients.

摘要

基因表达调控缺陷可能参与2型糖尿病的发病机制。我们已经通过胰岛素(3小时高胰岛素钳夹)对骨骼肌和皮下脂肪组织中10个与胰岛素作用相关基因的表达进行了协同调控的特征分析,并验证了在2型糖尿病患者的组织中是否会特异性地出现其中一些基因的调控缺陷。胰岛素受体、胰岛素受体底物-1、p85α磷脂酰肌醇3激酶(PI3K)、p110αPI3K、p110βPI3K、葡萄糖转运蛋白4(GLUT4)、糖原合酶和固醇调节元件结合蛋白-1c(SREBP-1c)的基础mRNA水平(通过逆转录-竞争性聚合酶链反应测定)在对照组(n = 17)、2型糖尿病患者(n = 9)、1型糖尿病患者(n = 9)和非糖尿病肥胖患者(n = 9)的肌肉中相似。在肌肉中,2型糖尿病患者的己糖激酶II表达降低(P < 0.01)。在脂肪组织中,肥胖(非糖尿病和2型糖尿病)患者的SREBP-1c(P < 0.01)mRNA表达降低,且与受试者的体重指数呈负相关(r = -0.63,P = 0.02)。胰岛素(±1000 pmol/l)在对照组、胰岛素抵抗的非糖尿病肥胖患者和高血糖的1型糖尿病受试者的肌肉和脂肪组织中诱导己糖激酶II、p85αPI3K和SREBP-1c mRNA水平增加两到三倍(P < 0.05)。在2型糖尿病患者中,这些基因的上调完全受阻。因此,本研究为2型糖尿病患者外周组织中一组重要基因对胰岛素反应的调控存在特异性缺陷提供了证据。

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