d-Fenfluramine and lorcaserin inhibit the binge-like feeding induced by μ-opioid receptor stimulation of the nucleus accumbens in the rat.

Highlights • We examined if 5-HT-based anorectic treatment reversed NAcc-driven feeding in the rat. • NAcc μ-opioid receptor stimulation followed systemic d -fenfluramine or lorcaserin. • Systemic d -fenfluramine or lorcaserin treatment reduced vegetable shortening intake. • d -fenfluramine or lorcaserin blocked NAcc μ-opioid enhancement of fat intake. • Systemic serotonin-based anorectics inhibit feeding promoted by brain reward circuits. Abstract Multiple laboratories have shown that the stimulation of μ-opioid receptors in the nucleus accumbens (NAcc) powerfully increases intake of palatable and high-fat diets. Separate studies have demonstrated that serotonin agonists advance satiety processes, and several serotonin-targeting agents have been prescribed to promote weight loss. However, it is unknown if serotonin signaling can modulate the increased feeding elicited by activation of NAcc μ-opioid receptors. These experiments assessed the effects of systemic treatments with the serotonin agonists d -fenfluramine and lorcaserin on the binge-like feeding induced by μ-opioid receptor stimulation of the NAcc in Sprague-Dawley rats. Consistent with previous reports, stimulation of NAcc μ-opioid receptors (with 0.025 μg/0.5 μl/side DAMGO) significantly increased consumption of high-fat vegetable shortening, and systemic treatment with d -fenfluramine and lorcaserin dose-dependently decreased intake. Interestingly, d -fenfluramine and lorcaserin reversed the binge-like feeding observed following stimulation of NAcc μ-opioid receptors. Both serotonergic drugs also attenuated the increases of ambulation observed following administration of DAMGO in the NAcc. These data demonstrate that serotonergic anorectics, in addition to their known role in advancing satiety processes during normal feeding, can also inhibit the binge-like feeding that is elicited by activation of μ-opioid receptors within the ventral striatum. [ABSTRACT FROM AUTHOR]