A single dorsal vagal complex circuit mediates the aversive and anorectic responses to GLP1R agonists.

Abstract

GLP-1 receptor agonists (GLP1RAs) effectively reduce feeding to treat obesity, although nausea and other aversive side effects of these drugs can limit their use. Brainstem circuits that promote satiation and that mediate the physiologic control of body weight can be distinguished from those that cause aversion. It remains unclear whether brainstem Glp1r neurons contribute to the normal regulation of energy balance and whether GLP1RAs control appetite via circuits distinct from those that mediate aversive responses, however. Hence, we defined roles for AP and NTS Glp1r -expressing neurons (AP ^Glp1r and NTS ^Glp1r neurons, respectively) in the physiologic control of body weight, the GLP1RA-dependent suppression of food intake, and the GLP1RA-mediated stimulation of aversive responses. While silencing non-aversive NTS ^Glp1r neurons interfered with the physiologic restraint of feeding and body weight, restoring NTS ^Glp1r neuron Glp1r expression on an otherwise Glp1r -null background failed to enable long-term body weight suppression by GLP1RAs. In contrast, selective Glp1r expression in AP ^Glp1r neurons restored both aversive responses and long-term body weight suppression by GLP1RAs. Thus, while non-aversive NTS ^Glp1r neurons control physiologic feeding, aversive AP ^Glp1r neurons mediate both the anorectic and weight loss effects of GLP1RAs, dictating the functional inseparability of these pharmacologic GLP1RA responses at a circuit level.