G Protein-Coupled Receptor 17 (Gpr17) Enhances Leptin and Insulin Sensitivity in Lean and Obese Mouse Models.

Abstract

Obesity, a major driver for diabetes development, is characterized by insulin and leptin resistance. We previously showed that loss of G protein-coupled receptor 17 (Gpr17) in specific hypothalamic neurons and the intestine led to better energy balance and glucose metabolism. Our goal is to test whether general loss of Gpr17 enhances insulin and leptin sensitivity. We generated germline Gpr17 knockout mice on both lean (Gpr17 ^-/- ) and obese (Gpr17 ^-/- ; ob/ob) backgrounds and characterized their metabolic profile. Gpr17 ^-/- mice exhibited increased energy expenditure and oxygen consumption. Euglycemic-hyperinsulinemic clamp studies showed enhanced insulin sensitivity in Gpr17 ^-/- mice with increased glycogen synthesis and decreased glycolysis. Gpr17 ^-/- ob/ob mice had increased insulin sensitivity with lower baseline serum insulin and higher response to exogenous leptin treatment with more reduction in feeding and increased pStat3 activation in hypothalamic nuclei. These findings highlight the inhibitory effect of Gpr17 in leptin and insulin sensitivity, suggesting its potential as a therapeutic target for obesity treatment.