4.8 Article

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

Journal

MOLECULAR PSYCHIATRY
Volume 25, Issue 5, Pages 1006-1021

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41380-019-0506-1

Keywords

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Funding

  1. NIH [K99DK107008, R01DK111436, R01ES027544, R21CA215591]
  2. American Diabetes Association [1-17-PDF-138]
  3. American Heart Association [17GRNT32960003, 16GRNT30970064, 16POST27260254]
  4. National Natural Science Foundation of China [81400886]
  5. Hubei Province health and family planning scientific research project [WJ2015Q033]
  6. Population and Family Planning Commission of Wuhan [WX14B34]
  7. Wuhan Young & Middle-Aged Talents, Health and Family Planning Commission of Wuhan Municipality
  8. China Scholarship Council [201608420019]
  9. USDA/CRIS [6250-51000-059-04S]

Ask authors/readers for more resources

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 (POMCARH neurons) associated with decreased neural activities of dopamine neurons in the ventral tegmental area (DA(VTA) neurons). We further revealed that POMCARH 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 POMCARH -> 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.

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