Author/Authors :
Da Young Oh، نويسنده , , Saswata Talukdar، نويسنده , , Eun Ju Bae، نويسنده , , Takeshi Imamura، نويسنده , , Hidetaka Morinaga، نويسنده , , WuQiang Fan، نويسنده , , Pingping Li، نويسنده , , Wendell J. Lu، نويسنده , , Steven M. Watkins، نويسنده , , Jerrold M. Olefsky، نويسنده ,
Abstract :
Omega-3 fatty acids (ω-3 FAs), DHA and EPA, exert anti-inflammatory effects, but the mechanisms are poorly understood. Here, we show that the G protein-coupled receptor 120 (GPR120) functions as an ω-3 FA receptor/sensor. Stimulation of GPR120 with ω-3 FAs or a chemical agonist causes broad anti-inflammatory effects in monocytic RAW 264.7 cells and in primary intraperitoneal macrophages. All of these effects are abrogated by GPR120 knockdown. Since chronic macrophage-mediated tissue inflammation is a key mechanism for insulin resistance in obesity, we fed obese WT and GPR120 knockout mice a high-fat diet with or without ω-3 FA supplementation. The ω-3 FA treatment inhibited inflammation and enhanced systemic insulin sensitivity in WT mice, but was without effect in GPR120 knockout mice. In conclusion, GPR120 is a functional ω-3 FA receptor/sensor and mediates potent insulin sensitizing and antidiabetic effects in vivo by repressing macrophage-induced tissue inflammation.