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CB(1) cannabinoid receptor in SF1-expressing neurons of the ventromedial hypothalamus determines metabolic responses to diet and leptin

Metabolic flexibility allows rapid adaptation to dietary change, however, little is known about the CNS mechanisms regulating this process. Neurons in the hypothalamic ventromedial nucleus (VMN) participate in energy balance and are the target of the metabolically relevant hormone leptin. Cannabinoi...

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Detalles Bibliográficos
Autores principales: Cardinal, Pierre, André, Caroline, Quarta, Carmelo, Bellocchio, Luigi, Clark, Samantha, Elie, Melissa, Leste-Lasserre, Thierry, Maitre, Marlene, Gonzales, Delphine, Cannich, Astrid, Pagotto, Uberto, Marsicano, Giovanni, Cota, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4209357/
https://www.ncbi.nlm.nih.gov/pubmed/25352999
http://dx.doi.org/10.1016/j.molmet.2014.07.004
Descripción
Sumario:Metabolic flexibility allows rapid adaptation to dietary change, however, little is known about the CNS mechanisms regulating this process. Neurons in the hypothalamic ventromedial nucleus (VMN) participate in energy balance and are the target of the metabolically relevant hormone leptin. Cannabinoid type-1 (CB(1)) receptors are expressed in VMN neurons, but the specific contribution of endocannabinoid signaling in this neuronal population to energy balance regulation is unknown. Here we demonstrate that VMN CB(1) receptors regulate metabolic flexibility and actions of leptin. In chow-fed mice, conditional deletion of CB(1) in VMN neurons (expressing the steroidogenic factor 1, SF1) decreases adiposity by increasing sympathetic activity and lipolysis, and facilitates metabolic effects of leptin. Conversely, under high-fat diet, lack of CB(1) in VMN neurons produces leptin resistance, blunts peripheral use of lipid substrates and increases adiposity. Thus, CB(1) receptors in VMN neurons provide a molecular switch adapting the organism to dietary change.