Targeting GPR120 and other fatty acid-sensing GPCRs ameliorates insulin resistance and inflammatory diseases

被引:250
作者
Talukdar, Saswata [1 ]
Olefsky, Jerrold M. [1 ]
Osborn, Olivia [1 ]
机构
[1] Univ Calif San Diego, Dept Med, Div Endocrinol & Metab, La Jolla, CA 92093 USA
关键词
PROTEIN-COUPLED-RECEPTOR; PANCREATIC BETA-CELLS; SECRETION IN-VIVO; PRESCRIPTION OMEGA-3-FATTY-ACIDS; ENTEROENDOCRINE CELLS; PEPTIDE-1; SECRETION; GLUCOSE-TOLERANCE; GUT MICROBIOTA; BREAST-CANCER; COLON-CANCER;
D O I
10.1016/j.tips.2011.04.004
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
The past decade has seen great progress in the understanding of the molecular pharmacology, physiological function and therapeutic potential of G-protein-coupled receptors (GPCRs). Free fatty acids (FFAs) have been demonstrated to act as ligands of several GPCRs including GPR40, GPR43, GPR84, GPR119 and GPR120. We have recently shown that GPR120 acts as a physiological receptor of omega 3 fatty acids in macrophages and c, which mediate potent anti-inflammatory and insulin sensitizing effects. The important role GPR120 plays in the control of inflammation raises the possibility that targeting this receptor could have therapeutic potential in many inflammatory diseases including obesity and type 2 diabetes. In this review paper, we discuss lipid-sensing GPCRs and highlight potential outcomes of targeting such receptors in ameliorating disease.
引用
收藏
页码:543 / 550
页数:8
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