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Asprosin is a centrally acting orexigenic hormone.

Abstract
Asprosin is a recently discovered fasting-induced hormone that promotes hepatic glucose production. Here we demonstrate that asprosin in the circulation crosses the blood-brain barrier and directly activates orexigenic AgRP+ neurons via a cAMP-dependent pathway. This signaling results in inhibition of downstream anorexigenic proopiomelanocortin (POMC)-positive neurons in a GABA-dependent manner, which then leads to appetite stimulation and a drive to accumulate adiposity and body weight. In humans, a genetic deficiency in asprosin causes a syndrome characterized by low appetite and extreme leanness; this is phenocopied by mice carrying similar mutations and can be fully rescued by asprosin. Furthermore, we found that obese humans and mice had pathologically elevated concentrations of circulating asprosin, and neutralization of asprosin in the blood with a monoclonal antibody reduced appetite and body weight in obese mice, in addition to improving their glycemic profile. Thus, in addition to performing a glucogenic function, asprosin is a centrally acting orexigenic hormone that is a potential therapeutic target in the treatment of both obesity and diabetes.
AuthorsClemens Duerrschmid, Yanlin He, Chunmei Wang, Chia Li, Juan C Bournat, Chase Romere, Pradip K Saha, Mark E Lee, Kevin J Phillips, Mahim Jain, Peilin Jia, Zhongming Zhao, Monica Farias, Qi Wu, Dianna M Milewicz, V Reid Sutton, David D Moore, Nancy F Butte, Michael J Krashes, Yong Xu, Atul R Chopra
JournalNature medicine (Nat Med) Vol. 23 Issue 12 Pg. 1444-1453 (Dec 2017) ISSN: 1546-170X [Electronic] United States
PMID29106398 (Publication Type: Journal Article)
Chemical References
  • Appetite Depressants
  • FBN1 protein, human
  • Fibrillin-1
  • Microfilament Proteins
  • Peptide Fragments
  • Peptide Hormones
Topics
  • Adolescent
  • Adult
  • Animals
  • Appetite Depressants (metabolism)
  • Appetite Regulation (genetics)
  • Female
  • Fibrillin-1
  • Humans
  • Hypothalamus (metabolism)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microfilament Proteins (genetics, physiology)
  • Neurons (metabolism)
  • Peptide Fragments (genetics, physiology)
  • Peptide Hormones (genetics, physiology)
  • Rats
  • Signal Transduction
  • Young Adult

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