Ludwig D S, Tritos N A, Mastaitis J W, Kulkarni R, Kokkotou E, Elmquist J, Lowell B, Flier J S, Maratos-Flier E
Department of Medicine, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
J Clin Invest. 2001 Feb;107(3):379-86. doi: 10.1172/JCI10660.
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.
多项研究表明,下丘脑神经肽黑色素浓缩激素(MCH)可调节哺乳动物的体重。缺乏功能性瘦素的肥胖小鼠在进食或禁食状态下MCH信息均过度表达。向大鼠脑室内急性注射MCH会增加其能量摄入。缺乏MCH基因的小鼠体型偏瘦。为了验证小鼠体内MCH长期过度表达会导致肥胖这一假说,我们培育了转基因小鼠,使其下丘脑外侧的MCH过度表达(MCH-OE),表达水平比正常小鼠高约两倍。在FVB基因背景下,喂食高脂饮食的纯合转基因动物在13周龄时比野生型动物多进食10%,体重重12%,且其体内瘦素水平更高。餐前及腹腔注射葡萄糖后,其血糖水平均较高。MCH-OE动物具有胰岛素抵抗,表现为血浆胰岛素水平显著升高且对胰岛素的反应减弱;给予胰岛素后,MCH-OE动物血糖仅下降5%,而野生型动物血糖下降31%。MCH-OE动物的胰岛大小也增加了两倍。为了评估基因背景对MCH-OE小鼠肥胖易感性的影响,将转基因培育到C57BL/6J基因背景上。表达转基因的杂合C57BL/6J小鼠在标准饮食下体重增加,证实MCH过度表达可导致肥胖。