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肥胖或肥胖合并 2 型糖尿病患者的人皮下脂肪小动脉功能障碍。

Dysfunction of human subcutaneous fat arterioles in obesity alone or obesity associated with Type 2 diabetes.

机构信息

Petru Poni Institute of Macromolecular Chemistry, Iasi, Romania.

出版信息

Clin Sci (Lond). 2011 May;120(10):463-72. doi: 10.1042/CS20100355.

Abstract

The aim of the present study was to examine the effects of obesity alone and obesity associated with Type 2 diabetes on the structure, vascular reactivity and response to insulin of isolated human subcutaneous fat arterioles; these effects were correlated with the expression of insulin signalling proteins. Periumbilical subcutaneous adipose tissue was explanted during surgery, small arterioles (internal diameter 220 ± 40 μm) were dissected out and investigated by electron microscopy, myography and immunoblotting. Compared with the subcutaneous arterioles of lean subjects, obesity activated the endothelium, enhanced the accumulation of collagen within vascular wall and increased the sensitivity of adrenergic response; obesity also diminished eNOS (endothelial NO synthase) protein expression, NO production, and endothelium-dependent and insulin-induced vasodilatation, as well as the protein expression of both IRS (insulin receptor substrates)-1 and IRS-2 and of the downstream molecules in the insulin signalling pathway, such as PI3K (phosphoinositide 3-kinase), phospho-Akt and Akt. When obesity was associated with Type 2 diabetes, these changes were significantly augmented. In conclusion, obesity alone or obesity associated with Type 2 diabetes alters human periumbilical adipose tissue arterioles in terms of structure, function and biochemsitry, including diminished eNOS expression and reduced levels of IRS-1, IRS-2, PI3K and Akt in the insulin signalling pathway.

摘要

本研究旨在探讨单纯肥胖症和肥胖症合并 2 型糖尿病对人体皮下脂肪小动脉结构、血管反应性和胰岛素反应的影响;并将这些影响与胰岛素信号蛋白的表达相关联。在手术过程中,从脐周皮下脂肪组织中分离出小动脉(内径 220±40μm),并通过电子显微镜、肌动描记术和免疫印迹法进行研究。与瘦素人群的皮下动脉相比,肥胖症激活了内皮细胞,增加了血管壁内胶原的积累,并增加了肾上腺素能反应的敏感性;肥胖症还降低了 eNOS(内皮型一氧化氮合酶)蛋白表达、NO 产生、内皮依赖性和胰岛素诱导的血管舒张以及胰岛素信号通路中 IRS(胰岛素受体底物)-1 和 IRS-2 的蛋白表达,以及 PI3K(磷酸肌醇 3-激酶)、磷酸化 Akt 和 Akt 等下游分子的蛋白表达。当肥胖症合并 2 型糖尿病时,这些变化显著增加。总之,单纯肥胖症或肥胖症合并 2 型糖尿病会改变人体脐周脂肪组织小动脉的结构、功能和生物化学特性,包括 eNOS 表达减少和胰岛素信号通路中 IRS-1、IRS-2、PI3K 和 Akt 水平降低。

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