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胰岛素抵抗的分子机制

Molecular mechanism of insulin resistance.

作者信息

Bhattacharya Samir, Dey Debleena, Roy Sib Sankar

机构信息

Cellular and Molecular Endocrinology Laboratory, Department of Zoology, School of Life Science, Visva-Bharati (A Central University), Santiniketan 731 235, India.

出版信息

J Biosci. 2007 Mar;32(2):405-13. doi: 10.1007/s12038-007-0038-8.

DOI:10.1007/s12038-007-0038-8
PMID:17435330
Abstract

Free fatty acids are known to play a key role in promoting loss of insulin sensitivity,thereby causing insulin resistance and type 2 diabetes.However,the underlying mechanism involved is still unclear.In searching for the cause of the mechanism,it has been found that palmitate inhibits insulin receptor (IR)gene expression,leading to a reduced amount of IR protein in insulin target cells. PDK1-independent phosphorylation of PKC(eta) causes this reduction in insulin receptor gene expression.One of the pathways through which fatty acid can induce insulin resistance in insulin target cells is suggested by these studies.We provide an overview of this important area,emphasizing the current status.

摘要

众所周知,游离脂肪酸在促进胰岛素敏感性丧失方面起着关键作用,从而导致胰岛素抵抗和2型糖尿病。然而,其中涉及的潜在机制仍不清楚。在寻找该机制的原因时,发现棕榈酸酯抑制胰岛素受体(IR)基因表达,导致胰岛素靶细胞中IR蛋白数量减少。PKC(η)的不依赖PDK1的磷酸化导致胰岛素受体基因表达的这种减少。这些研究提示了脂肪酸可在胰岛素靶细胞中诱导胰岛素抵抗的一种途径。我们概述了这一重要领域,并强调了当前的研究现状。

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本文引用的文献

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Involvement of novel PKC isoforms in FFA induced defects in insulin signaling.
Mol Cell Endocrinol. 2006 Feb 26;246(1-2):60-4. doi: 10.1016/j.mce.2005.12.014. Epub 2006 Jan 30.
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Inhibition of insulin receptor gene expression and insulin signaling by fatty acid: interplay of PKC isoforms therein.脂肪酸对胰岛素受体基因表达和胰岛素信号传导的抑制作用:蛋白激酶C亚型在其中的相互作用。
Cell Physiol Biochem. 2005;16(4-6):217-28. doi: 10.1159/000089847.
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Lack of the architectural factor HMGA1 causes insulin resistance and diabetes in humans and mice.缺乏结构因子HMGA1会导致人类和小鼠出现胰岛素抵抗及糖尿病。
抗逆转录病毒药物通过 miRNA 调控和 NLRP3 炎性小体的转录激活促进 HepG2 肝细胞胰岛素抵抗。
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The Neuronal and Non-Neuronal Pathways of Sodium-Glucose Cotransporter-2 Inhibitor on Body Weight-Loss and Insulin Resistance.钠-葡萄糖协同转运蛋白2抑制剂对体重减轻和胰岛素抵抗的神经元及非神经元通路
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