摘要
有毒脂类的积累是胰岛素抵抗2型糖尿病及相关代谢性疾病如肥胖和非酒精性脂肪肝最常见的病因。了解其潜在的机制,使得治疗代谢性疾病时以脂质代谢途径中的关键调控因子为靶标成为可能。本文总结了引起关键器官细胞内的脂质减少的潜在抗糖尿病药物的发现和发展过程,并特别强调了AMPK、SIRT1、PGC-1α、SREBP-1c、ChREBP、ACC、PPARs和HSPs蛋白,这些蛋白能促进脂肪酸氧化(能量消耗)或抑制脂质从头合成。
关键词: 抗糖尿病药物靶点,药物发现,胰岛素抵抗,脂质代谢。
图形摘要
Current Drug Targets
Title:Discovery of Novel Anti-Diabetic Drugs by Targeting Lipid Metabolism
Volume: 16 Issue: 12
Author(s): Xiu Zhou, Jun Xu, Yuguang Shi and Ji-Ming Ye
Affiliation:
关键词: 抗糖尿病药物靶点,药物发现,胰岛素抵抗,脂质代谢。
摘要: Accumulation of toxic lipids is the most common etiology of insulin resistance in type 2 diabetes and associated metabolic disorders such as obesity and non-alcoholic fatty liver disease. Understanding of the underlying mechanisms has revealed various opportunities to target key regulators in lipid metabolic pathways for the treatment of metabolic diseases. Here, we review the discovery and development of potential anti-diabetic drugs with primary effects on cellular targets leading to reductions of intracellular lipids in key organs. We will particularly focus on AMPK, SIRT1, PGC-1α, SREBP-1c, ChREBP, ACC, PPARs and HSPs which either stimulate in fatty acid oxidation (energy expenditure) or inhibit de novo lipogenesis.
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Cite this article as:
Xiu Zhou, Jun Xu, Yuguang Shi and Ji-Ming Ye , Discovery of Novel Anti-Diabetic Drugs by Targeting Lipid Metabolism, Current Drug Targets 2015; 16 (12) . https://dx.doi.org/10.2174/1389450116666150223120829
DOI https://dx.doi.org/10.2174/1389450116666150223120829 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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