GPR43: an emerging target for the potential treatment of type 2 diabetes, obesity and insulin resistance.

Atul Tiwari
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Abstract

A new role for fatty acids as endocrine regulators of lipid and carbohydrate metabolism through the activation of their cognate receptors, GPCRs, has been discovered during the past decade. GPR43 is a GPCR that has been implicated in the regulation of fatty-acid and glucose homeostasis in adipose tissue and the intestines, thus having potential therapeutic relevance in the treatment of type 2 diabetes, insulin resistance and obesity. Ongoing drug discovery efforts are focused toward the development of a novel, potent and selective orthosteric or allosteric modulator that acts as an agonist for GPR43. This review summarizes data supporting a role for GPR43 in the pharmacological management of metabolic disorders.

GPR43:潜在治疗2型糖尿病、肥胖和胰岛素抵抗的新靶点。
在过去的十年中,脂肪酸通过激活其同源受体GPCRs作为脂质和碳水化合物代谢的内分泌调节剂的新作用已经被发现。GPR43是一种与脂肪组织和肠道中脂肪酸和葡萄糖稳态调节有关的GPCR,因此在治疗2型糖尿病、胰岛素抵抗和肥胖方面具有潜在的治疗意义。正在进行的药物发现工作的重点是开发一种新的、有效的、选择性的正构或变构调节剂,作为GPR43的激动剂。这篇综述总结了支持GPR43在代谢紊乱的药理学管理中的作用的数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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