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受体裂解导致高血压胰岛素抵抗的新假说

A New Hypothesis for Insulin Resistance in Hypertension Due to Receptor Cleavage.

作者信息

Delano Frank A, Zhang Hanrui, Tran Edward E, Zhang Cuihua, Schmid-Schönbein Geert W

机构信息

Department of Bioengineering, The Whitaker Institute for Biomedical Engineering, University of California San Diego, La Jolla, CA 92093-0412, , Tel: 858 534 4276 (FAD), 206 362 3590 (EET), 858 534 3852 (GWSS).

出版信息

Expert Rev Endocrinol Metab. 2010 Jan 1;5(1):149-158. doi: 10.1586/eem.09.64.

Abstract

BACKGROUND

One of the most important unresolved issues in diabetes is the mechanism for the attenuated response to insulin, i.e. insulin resistance. AIMS AND METHODS: We hypothesize that the mechanism for the insulin resistance is due to uncontrolled protease activity in the plasma, on endothelial cells and in the tissue parenchyma. To examine this hypothesis we use of microzymographic techniques in the microcirculation, plasma zymography, and receptor labeling techniques with antibodies against an extracellular domain of the insulin receptor α. RESULTS: The spontaneously hypertensive rat has an enhanced proteolytic activity and significant cleavage of the receptor with attenuated glucose transport. We present evidence for insulin receptor cleavage in a high fat diet and a transgenic model of diabetes. CONCLUSION: These results suggest that cleavage of the extracellular domain of the insulin receptor, a situation that interferes with the ability for insulin to bind and provide an intracellular signal for glucose transport, may be involved in insulin resistance.

摘要

背景

糖尿病中最重要的未解决问题之一是对胰岛素反应减弱的机制,即胰岛素抵抗。目的和方法:我们假设胰岛素抵抗的机制是由于血浆、内皮细胞和组织实质中蛋白酶活性失控。为检验这一假设,我们在微循环中使用微酶谱技术、血浆酶谱分析以及用针对胰岛素受体α细胞外结构域的抗体进行受体标记技术。结果:自发性高血压大鼠具有增强的蛋白水解活性,且受体有显著裂解,同时葡萄糖转运减弱。我们提供了高脂肪饮食和糖尿病转基因模型中胰岛素受体裂解的证据。结论:这些结果表明,胰岛素受体细胞外结构域的裂解可能参与了胰岛素抵抗,这种情况会干扰胰岛素结合并为葡萄糖转运提供细胞内信号的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/73bb/2995254/0dae194f2a6e/nihms251790f1.jpg

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