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Food-induced dopamine signaling in AgRP neurons promotes feeding

Obesity comorbidities such as diabetes and cardiovascular disease are pressing public health concerns. Overconsumption of calories leads to weight gain; however, neural mechanisms underlying excessive food consumption are poorly understood. Here, we demonstrate that dopamine receptor D1 (Drd1) expre...

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Detalles Bibliográficos
Autores principales: Zhang, Qi, Tang, Qijun, Purohit, Nidhi M., Davenport, Julia B., Brennan, Charles, Patel, Rahul K., Godschall, Elizabeth, Zwiefel, Larry S., Spano, Anthony, Campbell, John N., Güler, Ali D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753708/
https://www.ncbi.nlm.nih.gov/pubmed/36450244
http://dx.doi.org/10.1016/j.celrep.2022.111718
Descripción
Sumario:Obesity comorbidities such as diabetes and cardiovascular disease are pressing public health concerns. Overconsumption of calories leads to weight gain; however, neural mechanisms underlying excessive food consumption are poorly understood. Here, we demonstrate that dopamine receptor D1 (Drd1) expressed in the agouti-related peptide/neuropeptide Y (AgRP/NPY) neurons of the arcuate hypothalamus is required for appropriate responses to a high-fat diet (HFD). Stimulation of Drd1 and AgRP/NPY co-expressing arcuate neurons is sufficient to induce voracious feeding. Delivery of a HFD after food deprivation acutely induces dopamine (DA) release in the ARC, whereas animals that lack Drd1 expression in ARC(AgRP/NPY) neurons (Drd1(AgRP)-KO) exhibit attenuated foraging and refeeding of HFD. These results define a role for the DA input to the ARC that encodes acute responses to food and position Drd1 signaling in the ARC(AgRP/NPY) neurons as an integrator of the hedonic and homeostatic neuronal feeding circuits.