| Literature DB >> 11867747 |
Donald J Marsh1, Drew T Weingarth, Dawn E Novi, Howard Y Chen, Myrna E Trumbauer, Airu S Chen, Xiao-Ming Guan, Michael M Jiang, Yue Feng, Ramon E Camacho, Zhu Shen, Easter G Frazier, Hong Yu, Joseph M Metzger, Stephanie J Kuca, Lauren P Shearman, Shobhna Gopal-Truter, Douglas J MacNeil, Alison M Strack, D Euan MacIntyre, Lex H T Van der Ploeg, Su Qian.
Abstract
Melanin-concentrating hormone (MCH) is a cyclic 19-aa hypothalamic neuropeptide derived from a larger prohormone precursor of MCH (Pmch), which also encodes neuropeptide EI (NEI) and neuropeptide GE (NGE). Pmch-deficient (Pmch-/-) mice are lean, hypophagic, and have an increased metabolic rate. Transgenic mice overexpressing Pmch are hyperphagic and develop mild obesity. Consequently, MCH has been implicated in the regulation of energy homeostasis. The MCH 1 receptor (MCH1R) is one of two recently identified G protein-coupled receptors believed to be responsible for the actions of MCH. We evaluated the physiological role of MCH1R by generating MCH1R-deficient (Mch1r-/-) mice. Mch1r-/- mice have normal body weights, yet are lean and have reduced fat mass. Surprisingly, Mch1r-/- mice are hyperphagic when maintained on regular chow, and their leanness is a consequence of hyperactivity and altered metabolism. Consistent with the hyperactivity, Mch1r-/- mice are less susceptible to diet-induced obesity. Importantly, chronic central infusions of MCH induce hyperphagia and mild obesity in wild-type mice, but not in Mch1r-/- mice. We conclude that MCH1R is a physiologically relevant MCH receptor in mice that plays a role in energy homeostasis through multiple actions on locomotor activity, metabolism, appetite, and neuroendocrine function.Entities:
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Year: 2002 PMID: 11867747 PMCID: PMC122503 DOI: 10.1073/pnas.052706899
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205