1. Feeding Induced by Cannabinoids Is Mediated Independently of the Melanocortin System
- Author
-
Verdejo García, A, Sinnayah, P, Jobst, EE, Rathner, JA, Caldera-Siu, AD, Tonelli-Lemos, L, Eusterbrock, AJ, Enriori, PJ, Pothos, EN, Grove, KL, Cowley, MA, Verdejo García, A, Sinnayah, P, Jobst, EE, Rathner, JA, Caldera-Siu, AD, Tonelli-Lemos, L, Eusterbrock, AJ, Enriori, PJ, Pothos, EN, Grove, KL, and Cowley, MA
- Abstract
BACKGROUND: Cannabinoids, the active components of marijuana, stimulate appetite, and cannabinoid receptor-1 (CB1-R) antagonists suppress appetite and promote weight loss. Little is known about how CB1-R antagonists affect the central neurocircuitry, specifically the melanocortin system that regulates energy balance. METHODOLOGY/PRINCIPAL FINDINGS: Here, we show that peripherally administered CB1-R antagonist (AM251) or agonist equally suppressed or stimulated feeding respectively in A(y) , which lack a functional melanocortin system, and wildtype mice, demonstrating that cannabinoid effects on feeding do not require melanocortin circuitry. CB1-R antagonist or agonist administered into the ventral tegmental area (VTA) equally suppressed or stimulated feeding respectively, in both genotypes. In addition, peripheral and central cannabinoid administration similarly induced c-Fos activation in brain sites suggesting mediation via motivational dopaminergic circuitry. Amperometry-detected increases in evoked dopamine (DA) release by the CB1-R antagonist in nucleus accumbens slices indicates that AM251 modulates DA release from VTA terminals. CONCLUSIONS/SIGNIFICANCE: Our results demonstrate that the effects of cannabinoids on energy balance are independent of hypothalamic melanocortin circuitry and is primarily driven by the reward system.
- Published
- 2008