Xu Baoji, Goulding Evan H, Zang Keling, Cepoi David, Cone Roger D, Jones Kevin R, Tecott Laurence H, Reichardt Louis F
Howard Hughes Medical Institute, University of California, San Francisco, California 94143, USA.
Nat Neurosci. 2003 Jul;6(7):736-42. doi: 10.1038/nn1073.
The melanocortin-4 receptor (MC4R) is critically involved in regulating energy balance, and obesity has been observed in mice with mutations in the gene for brain-derived neurotrophic factor (BDNF). Here we report that BDNF is expressed at high levels in the ventromedial hypothalamus (VMH) where its expression is regulated by nutritional state and by MC4R signaling. In addition, similar to MC4R mutants, mouse mutants that expresses the BDNF receptor TrkB at a quarter of the normal amount showed hyperphagia and excessive weight gain on higher-fat diets. Furthermore, BDNF infusion into the brain suppressed the hyperphagia and excessive weight gain observed on higher-fat diets in mice with deficient MC4R signaling. These results show that MC4R signaling controls BDNF expression in the VMH and support the hypothesis that BDNF is an important effector through which MC4R signaling controls energy balance.
黑皮质素-4受体(MC4R)在调节能量平衡中起关键作用,并且在脑源性神经营养因子(BDNF)基因发生突变的小鼠中观察到了肥胖现象。在此我们报告,BDNF在下丘脑腹内侧核(VMH)中高水平表达,其表达受营养状态和MC4R信号传导调控。此外,与MC4R突变体相似,将BDNF受体TrkB表达量降至正常水平四分之一的小鼠突变体在高脂饮食时出现摄食过量和体重过度增加。此外,向大脑中注入BDNF可抑制MC4R信号传导缺陷的小鼠在高脂饮食时出现的摄食过量和体重过度增加。这些结果表明,MC4R信号传导控制VMH中BDNF的表达,并支持BDNF是MC4R信号传导控制能量平衡的重要效应因子这一假说。