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药物还是饮食?——开发针对GPCRs游离脂肪酸家族的新型治疗策略

Drugs or diet?--Developing novel therapeutic strategies targeting the free fatty acid family of GPCRs.

作者信息

Dranse H J, Kelly M E M, Hudson B D

机构信息

Department of Pharmacology, Dalhousie University, Halifax, NS, Canada.

出版信息

Br J Pharmacol. 2013 Oct;170(4):696-711. doi: 10.1111/bph.12327.

Abstract

Free fatty acids (FFAs) are metabolic intermediates that may be obtained through the diet, synthesized endogenously, or produced via fermentation of carbohydrates by gut microbiota. In addition to serving as an important source of energy, FFAs are known to produce a variety of both beneficial and detrimental effects on metabolic and inflammatory processes. While historically, FFAs were believed to produce these effects only through intracellular targets such as peroxisome proliferator-activated receptors, it has now become clear that FFAs are also agonists for several GPCRs, including a family of four receptors now termed FFA1-4. Increasing evidence suggests that FFA1-4 mediate many of the beneficial properties of FFAs and not surprisingly, this has generated significant interest in the potential of these receptors as therapeutic targets for the treatment of a variety of metabolic and inflammatory disorders. In addition to the traditional strategy of developing small-molecule therapeutics targeting these receptors, there has also been some consideration given to alternate therapeutic approaches, specifically by manipulating endogenous FFA concentrations through alteration of either dietary intake, or production by gut microbiota. In this review, the current state of knowledge for FFA1-4 will be discussed, together with their potential as therapeutic targets in the treatment of metabolic and inflammatory disorders. In particular, the evidence in support of small molecule versus dietary and microbiota-based therapeutic approaches will be considered to provide insight into the development of novel multifaceted strategies targeting the FFA receptors for the treatment of metabolic and inflammatory disorders.

摘要

游离脂肪酸(FFAs)是一种代谢中间产物,可通过饮食获取、内源性合成或由肠道微生物群对碳水化合物进行发酵产生。除了作为重要的能量来源外,游离脂肪酸还已知会对代谢和炎症过程产生各种有益和有害的影响。从历史上看,游离脂肪酸被认为仅通过细胞内靶点(如过氧化物酶体增殖物激活受体)产生这些作用,但现在已经清楚的是,游离脂肪酸也是几种G蛋白偶联受体(GPCRs)的激动剂,包括现在称为FFA1 - 4的四个受体家族。越来越多的证据表明,FFA1 - 4介导了游离脂肪酸的许多有益特性,不出所料,这引发了人们对这些受体作为治疗各种代谢和炎症性疾病的潜在靶点的极大兴趣。除了开发针对这些受体的小分子疗法的传统策略外,还考虑了其他治疗方法,特别是通过改变饮食摄入量或肠道微生物群的产生来调节内源性游离脂肪酸浓度。在这篇综述中,将讨论FFA1 - 4的当前知识状态,以及它们作为治疗代谢和炎症性疾病的潜在靶点。特别是,将考虑支持小分子疗法与基于饮食和微生物群的治疗方法的证据,以深入了解针对FFA受体开发新型多方面策略来治疗代谢和炎症性疾病。

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