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Melanin-concentrating hormone overexpression in transgenic mice leads to obesity and insulin resistance
David S. Ludwig, … , Jeffrey S. Flier, Eleftheria Maratos-Flier
David S. Ludwig, … , Jeffrey S. Flier, Eleftheria Maratos-Flier
Published February 1, 2001
Citation Information: J Clin Invest. 2001;107(3):379-386. https://doi.org/10.1172/JCI10660.
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Article

Melanin-concentrating hormone overexpression in transgenic mice leads to obesity and insulin resistance

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Abstract

Several lines of investigation suggest that the hypothalamic neuropeptide melanin-concentrating hormone (MCH) regulates body weight in mammals. Obese mice lacking functional leptin overexpress the MCH message in the fed or fasted state. Acute intracerebroventricular injection of MCH increases energy intake in rats. Mice lacking the MCH gene are lean. To test the hypothesis that chronic overexpression of MCH in mice causes obesity, we produced transgenic mice that overexpress MCH (MCH-OE) in the lateral hypothalamus at approximately twofold higher levels than normal mice. On the FVB genetic background, homozygous transgenic animals fed a high-fat diet ate 10% more and were 12% heavier at 13 weeks of age than wild-type animals, and they had higher systemic leptin levels. Blood glucose levels were higher both preprandially and after an intraperitoneal glucose injection. MCH-OE animals were insulin-resistant, as demonstrated by markedly higher plasma insulin levels and a blunted response to insulin; MCH-OE animals had only a 5% decrease in blood glucose after insulin administration, compared with a 31% decrease in wild-type animals. MCH-OE animals also exhibited a twofold increase in islet size. To evaluate the contribution of genetic background to the predisposition to obesity seen in MCH-OE mice, the transgene was bred onto the C57BL/6J background. Heterozygote C57BL/6J mice expressing the transgene showed increased body weight on a standard diet, confirming that MCH overexpression can lead to obesity.

Authors

David S. Ludwig, Nicholas A. Tritos, Jason W. Mastaitis, Rohit Kulkarni, Efi Kokkotou, Joel Elmquist, Bradford Lowell, Jeffrey S. Flier, Eleftheria Maratos-Flier

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Figure 3

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(a and b) A series of bright-field photomicrographs demonstrate MCH-immu...
(a and b) A series of bright-field photomicrographs demonstrate MCH-immunoreactive neurons in the lateral hypothalamic area (LHA) in the brain (a) of an MCH-OE mouse (mouse Tg-12) and in the corresponding hypothalamic area in the brain (b) of a wild-type mouse (mouse Tg-7), showing a visually evident increase in MCH immunostaining in neurons of the MCH-OE mouse in comparison with the wild-type mouse. (c and d) A series of dark-field photomicrographs demonstrate the distribution of MCH-immunoreactive fibers in the LHA in the brain (c) of an MCH-transgenic mouse (mouse Tg-12) and in the corresponding hypothalamic area in the brain (d) of a wild-type mouse (mouse Tg-7). Within the LHA, the MCH-immunoreactive cell bodies are distributed in similar patterns in the MCH-OE and wild-type brains (c and d). However, note the visually apparent increase in MCH immunoreactivity in the LHA (c and d). There is also visually evident increase in MCH immunoreactivity surrounding the paraventricular hypothalamic nucleus (PVH) in the MCH-OE brain (bottom left panel) compared with the wild-type brain (bottom right panel). Scale bar, 200 μm. cp, cerebral peduncle; fx, fornix; ot, optic tract; 3v, third ventricle.

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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