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GPR119 a novel G protein-coupled receptor target for the treatment of type 2 diabetes and obesity

机译:GPR119一种用于治疗2型糖尿病和肥胖症的新型G蛋白偶联受体靶标

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摘要

GPR119 is a G protein-coupled receptor expressed predominantly in the pancreas (β-cells) and gastrointestinal tract (enteroendocrine cells) in humans. De-orphanization of GPR119 has revealed two classes of possible endogenous ligands, viz., phospholipids and fatty acid amides. Of these, oleoylethanolamide (OEA) is one of the most active ligands tested so far. This fatty acid ethanolamide is of particular interest because of its known effects of reducing food intake and body weight gain when administered to rodents. Agonists at the GPR119 receptor cause an increase in intracellular cAMP levels via Gαs coupling to adenylate cyclase. In vitro studies have indicated a role for GPR119 in the modulation of insulin release by pancreatic β-cells and of GLP-1 secretion by gut enteroendocrine cells. The effects of GPR119 agonists in animal models of diabetes and obesity are reviewed, and the potential value of such compounds in future therapies for these conditions is discussed.
机译:GPR119是一种G蛋白偶联受体,主要在人类的胰腺(β细胞)和胃肠道(内分泌细胞)中表达。 GPR119的去孤儿化显示出两类可能的内源性配体,即磷脂和脂肪酸酰胺。其中,油酰乙醇酰胺(OEA)是迄今为止测试的最具活性的配体之一。这种脂肪酸乙醇酰胺具有特别的意义,因为它在啮齿动物中具有减少食物摄入和增加体重的已知作用。 GPR119受体的激动剂通过与α腺苷酸环化酶偶联的Gα引起细胞内cAMP水平的升高。体外研究表明,GPR119在调节胰岛β细胞释放胰岛素和肠道肠内分泌细胞分泌GLP-1中发挥作用。审查了GPR119激动剂在糖尿病和肥胖动物模型中的作用,并讨论了此类化合物在未来治疗中针对这些疾病的潜在价值。

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