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APPETITE, OBESITY, DIGESTION, AND METABOLISM

Mice with MCH ablation resist diet-induced obesity through strain-specific mechanisms

¹Joslin Diabetes Center, Boston, Massachussetts; ²Division of Endocrinology, ³Division of Gastroenterology, ⁴Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston Massachusetts

Submitted 23 December 2004 ; accepted in final form 17 February 2005

Genetics and environment contribute to the development of obesity, in both humans and rodents. However, the potential interaction between genes important in energy balance, strain background, and dietary environment has been only minimally explored. We investigated the effects of genetic ablation of melanin-concentrating hormone (MCH), a neuropeptide with a key role in energy balance, with chow and a high-fat diet (HFD) in two different mouse strains, one obesity-prone (C57BL/6) and the other obesity-resistant (129). Substantial differences were seen in wild-type (WT) animals of different strains. 129 animals had significantly lower levels of spontaneous locomotor activity than C57BL/6; however, 129 mice gained less weight on both chow and HFD. In both strains, deletion of MCH led to attenuated weight gain compared with WT counterparts, an effect secondary to increased energy expenditure. In both strains, feeding a HFD led to further increases in energy expenditure in both WT and MCH-KO mice; however, this increase was more pronounced in 129 mice. In addition, mice lacking MCH have a phenotype of increased locomotor activity, an effect also seen in both strains. The relative increase in activity in MCH^–/– mice is modest in animals fed chow but increases substantially when animals are placed on HFD. These studies reinforce the important role of MCH in energy homeostasis and indicate that MCH is a plausible target for antiobesity therapy.

melanin-concentrating hormone; obesity; hypothalamus; diet-induced obesity; 129; C57Bl/6; strains; locomotor activity; energy expenditure

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