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A POMC-originated circuit regulates stress-induced hypophagia, depression and anhedonia

Chronic stress causes dysregulations of mood and energy homeostasis, but the neurocircuitry underlying these alterations remain to be fully elucidated. Here we demonstrate that chronic restraint stress in mice results in hyperactivity of pro-opiomelanocortin neurons in the arcuate nucleus of the hyp...

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Detalles Bibliográficos
Autores principales: Qu, Na, He, Yanlin, Wang, Chunmei, Xu, Pingwen, Yang, Yongjie, Cai, Xing, Liu, Hesong, Yu, Kaifan, Pei, Zhou, Hyseni, Ilirjana, Sun, Zheng, Fukuda, Makoto, Li, Yi, Tian, Qing, Xu, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7056580/
https://www.ncbi.nlm.nih.gov/pubmed/31485012
http://dx.doi.org/10.1038/s41380-019-0506-1
Descripción
Sumario:Chronic stress causes dysregulations of mood and energy homeostasis, but the neurocircuitry underlying these alterations remain to be fully elucidated. Here we demonstrate that chronic restraint stress in mice results in hyperactivity of pro-opiomelanocortin neurons in the arcuate nucleus of the hypothalamus (POMC(ARH) neurons) associated with decreased neural activities of dopamine neurons in the ventral tegmental area (DA(VTA) neurons). We further revealed that POMC(ARH) neurons project to the VTA and provide an inhibitory tone to DA(VTA) neurons via both direct and indirect neurotransmissions. Finally, we show that photoinhibition of the POMC(ARH)→VTA circuit in mice increases body weight and food intake, and reduces depression-like behaviors and anhedonia in mice exposed to chronic restraint stress. Thus, our results identified a novel neurocircuitry regulating feeding and mood in response to stress.