Melanin-concentrating hormone 1 receptor-deficient mice are lean, hyperactive, and hyperphagic and have altered metabolism

被引:474
作者
Marsh, DJ
Weingarth, DT
Novi, DE
Chen, HY
Trumbauer, ME
Chen, AS
Guan, XM
Jiang, MM
Feng, Y
Camacho, RE
Shen, Z
Frazier, EG
Yu, H
Metzger, JM
Kuca, SJ
Shearman, LP
Gopal-Truter, S
MacNeil, DJ
Strack, AM
MacIntyre, DE
Van der Ploeg, LHT
Qian, S [1 ]
机构
[1] Merck Res Labs, Dept Obes Res, Rahway, NJ 07065 USA
[2] Merck Res Labs, Dept Anim Pharmacol, Rahway, NJ 07065 USA
[3] Merck Res Labs, Dept Comparat Med, Rahway, NJ 07065 USA
关键词
D O I
10.1073/pnas.052706899
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Melanin-concentrating hormone (MCH) is a cyclic 19-aa hypothalamic neuropeptide derived from a larger prohormone precursor of MCH (Pmch), which also encodes neuropeptide El (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.
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页码:3240 / 3245
页数:6
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