Peripheral actions of GPCRs in energy homeostasis: view from the Chair.

International journal of obesity supplements Pub Date : 2014-07-01 Epub Date: 2014-07-08 DOI:10.1038/ijosup.2014.2
M Bouvier
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引用次数: 0

Abstract

The roles of G-protein-coupled receptors (GPCRs) in the control of food intake and energy expenditure are being increasingly recognized, and new drug candidates targeting these receptors are making their entry into the clinic. GPCRs exert their action along the various sites of regulation of energy homeostasis control including the central nervous system, the pancreas, the gut and fat cells. Exciting new data about GPCRs recognizing and mediating the effects of lipid mediators and concerning receptors for which no endogenous ligands have been identified yet open new exciting avenues for the validation of additional drug targets. In addition, recently developed paradigms around the concepts of cross-talk regulation and functional selectivity should lead to the development of drugs with improved therapeutic efficacy and reduced undesirable effects. Some of these promising discoveries are discussed in the present article and accompanying papers.

gpcr在能量稳态中的外周作用:主席的观点。
g蛋白偶联受体(gpcr)在控制食物摄入和能量消耗中的作用越来越被认识到,针对这些受体的新候选药物正在进入临床。GPCRs在能量稳态控制的各种调控位点发挥作用,包括中枢神经系统、胰腺、肠道和脂肪细胞。关于gpcr识别和介导脂质介质作用的令人兴奋的新数据,以及尚未确定内源性配体的受体,为验证其他药物靶点开辟了令人兴奋的新途径。此外,最近围绕串扰调节和功能选择性概念开发的范式应该会导致开发出具有提高治疗效果和减少不良反应的药物。本文和随附的论文讨论了其中一些有希望的发现。
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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