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Diabetes and obesity during pregnancy alter insulin signalling and glucose transporter expression in maternal skeletal muscle and subcutaneous adipose tissue

机译:怀孕期间的糖尿病和肥胖会改变孕妇骨骼肌和皮下脂肪组织中的胰岛素信号传导和葡萄糖转运蛋白表达

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Severe insulin resistance is a defining attribute of gestational diabetes mellitus (GDM). It is postulated that alterations in the insulin-signalling pathway and subsequent glucose disposal are the underlying cause of insulin resistance in patients with GDM. The purpose of this study was to profile the insulin-signalling pathway and intermediates in insulin-sensitive tissues. Subcutaneous adipose tissue and skeletal muscle were collected from normal glucose-tolerant (NGT) and insulin-controlled GDM in both non-obese and obese cohorts (n=6–8 per subgroup). Expression studies of the insulin-signalling pathway were performed using western blotting and quantitative reverse transcription-PCR. This study demonstrated altered mRNA expression of insulin receptor substrate (IRS)-1, IRS-2, glucose transporter (GLUT)-1, GLUT-4 and glycogen synthase kinase (GSK)-3 isoforms genes in adipose tissue in GDM women in comparison to NGT pregnant controls. In skeletal muscle, insulin-controlled GDM was associated with decreased IRS-1, phosphatidylinositol-3-kinase (PI3-K) p85α, GLUT-1 and -4, GSK-3 isoforms and phosphoinositide-dependent kinase-1. Both adipose tissue and skeletal muscle from women with GDM displayed decreased IRS-1 and GLUT-4 and increased PI3-K p85α protein expression. Both skeletal muscle and adipose tissue from obese women demonstrated lower GLUT-1 and -4 mRNA expression and diminished GLUT-4 protein expression in skeletal muscle only. Collectively, our results suggest that diabetes and obesity during pregnancy cause defects in insulin-signalling transduction in adipose tissue and skeletal muscle and may be the underlying cause of GDM.
机译:严重的胰岛素抵抗是妊娠糖尿病(GDM)的定义属性。据推测,胰岛素信号通路的改变和随后的葡萄糖处置是GDM患者胰岛素抵抗的根本原因。这项研究的目的是概述胰岛素敏感组织中的胰岛素信号通路和中间体。在非肥胖和肥胖人群中,从正常的葡萄糖耐量(NGT)和胰岛素控制的GDM中收集皮下脂肪组织和骨骼肌(每组n = 6-8)。使用蛋白质印迹和定量逆转录-PCR进行了胰岛素信号通路的表达研究。这项研究表明,相比之下,GDM妇女脂肪组织中胰岛素受体底物(IRS)-1,IRS-2,葡萄糖转运蛋白(GLUT)-1,GLUT-4和糖原合酶激酶(GSK)-3同工型基因的mRNA表达发生了变化NGT孕妇对照组。在骨骼肌中,胰岛素控制的GDM与IRS-1,磷脂酰肌醇3-激酶(PI3-K)p85α,GLUT-1和-4,GSK-3亚型和磷酸肌醇依赖性激酶1降低有关。 GDM妇女的脂肪组织和骨骼肌均显示IRS-1和GLUT-4减少,PI3-Kp85α蛋白表达增加。肥胖妇女的骨骼肌和脂肪组织都仅在骨骼肌中显示出较低的GLUT-1和-4 mRNA表达,并减少了GLUT-4蛋白表达。总体而言,我们的研究结果表明,妊娠期糖尿病和肥胖症会引起脂肪组织和骨骼肌中胰岛素信号转导的缺陷,并且可能是GDM的根本原因。

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