Department of Pharmacy, College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul, Republic of Korea.
Department of Pharmacy, College of Pharmacy and Institute of Pharmaceutical Science and Technology, Hanyang University, Ansan, Republic of Korea.
Diabetes Obes Metab. 2018 Feb;20(2):257-269. doi: 10.1111/dom.13062. Epub 2017 Aug 22.
GPR119 belongs to the G protein-coupled receptor family and exhibits dual modes of action upon ligand-dependent activation: pancreatic secretion of insulin in a glucose-dependent manner and intestinal secretion of incretins. Hence, GPR119 has emerged as a promising target for treating type 2 diabetes mellitus without causing hypoglycaemia. However, despite continuous efforts by many major pharmaceutical companies, no synthetic GPR119 ligand has been approved as a new class of anti-diabetic agents thus far, nor has any passed beyond phase II clinical studies. Herein, we summarize recent advances in research concerning the physiological/pharmacological effects of GPR119 and its synthetic ligands on the regulation of energy metabolism, and we speculate on future applications of GPR119 ligands for the treatment of metabolic diseases, focusing on non-alcoholic fatty liver disease.
GPR119 属于 G 蛋白偶联受体家族,在配体依赖性激活后表现出双重作用模式:以葡萄糖依赖的方式促进胰岛素的胰腺分泌和肠促胰岛素的分泌。因此,GPR119 已成为治疗 2 型糖尿病而不引起低血糖的有前途的靶点。然而,尽管许多大型制药公司不断努力,迄今为止,没有任何合成的 GPR119 配体被批准为新型抗糖尿病药物,也没有任何药物超过 II 期临床研究。本文总结了 GPR119 及其合成配体在调节能量代谢方面的生理/药理学作用的最新研究进展,并推测 GPR119 配体在治疗代谢性疾病(重点是非酒精性脂肪性肝病)方面的未来应用。