Ito Masahiko, Gomori Akira, Ishihara Akane, Oda Zenjun, Mashiko Satoshi, Matsushita Hiroko, Yumoto Mariko, Ito Makoto, Sano Hideki, Tokita Shigeru, Moriya Minoru, Iwaasa Hisashi, Kanatani Akio
Tsukuba Research Institute, Banyu Pharmaceutical Co., Ltd., Okubo 3, Tsukuba 300-2611, Japan.
Am J Physiol Endocrinol Metab. 2003 May;284(5):E940-5. doi: 10.1152/ajpendo.00529.2002. Epub 2003 Jan 28.
Melanin-concentrating hormone (MCH) is a cyclic orexigenic peptide expressed in the lateral hypothalamus. Recently, we demonstrated that chronic intracerebroventricular infusion of MCH induced obesity accompanied by sustained hyperphagia in mice. Here, we analyzed the mechanism of MCH-induced obesity by comparing animals fed ad libitum with pair-fed and control animals. Chronic infusion of MCH significantly increased food intake, body weight, white adipose tissue (WAT) mass, and liver mass in ad libitum-fed mice on a moderately high-fat diet. In addition, a significant increase in lipogenic activity was observed in the WAT of the ad libitum-fed group. Although body weight gain was marginal in the pair-fed group, MCH infusion clearly enhanced the lipogenic activity in liver and WAT. Plasma leptin levels were also increased in the pair-fed group. Furthermore, MCH infusion significantly reduced rectal temperatures in the pair-fed group. In support of these findings, mRNA expression of uncoupling protein-1, acyl-CoA oxidase, and carnitine palmitoyltransferase I, which are key molecules involved in thermogenesis and fatty acid oxidation, were reduced in the brown adipose tissue (BAT) of the pair-fed group, suggesting that MCH infusion might reduce BAT functions. We conclude that the activation of MCH neuronal pathways stimulated adiposity, in part resulting from increased lipogenesis in liver and WAT and reduced energy expenditure in BAT. These findings confirm that modulation of energy homeostasis by MCH may play a critical role in the development of obesity.
黑色素聚集激素(MCH)是一种在下丘脑外侧表达的环型促食欲肽。最近,我们证明了慢性脑室内注入MCH会诱导小鼠肥胖,并伴有持续的摄食过多。在此,我们通过比较自由进食的动物与配对喂养及对照动物,分析了MCH诱导肥胖的机制。在适度高脂肪饮食下,慢性注入MCH显著增加了自由进食小鼠的食物摄入量、体重、白色脂肪组织(WAT)质量和肝脏质量。此外,在自由进食组的WAT中观察到生脂活性显著增加。虽然配对喂养组的体重增加不明显,但MCH注入明显增强了肝脏和WAT中的生脂活性。配对喂养组的血浆瘦素水平也有所升高。此外,MCH注入显著降低了配对喂养组的直肠温度。作为这些发现的佐证,参与产热和脂肪酸氧化的关键分子解偶联蛋白-1、酰基辅酶A氧化酶和肉碱棕榈酰转移酶I的mRNA表达在配对喂养组的棕色脂肪组织(BAT)中降低,这表明MCH注入可能会降低BAT的功能。我们得出结论,MCH神经元通路的激活刺激了肥胖,部分原因是肝脏和WAT中生脂增加以及BAT中能量消耗减少。这些发现证实,MCH对能量稳态的调节可能在肥胖的发展中起关键作用。