Iwakoshi-Ukena Eiko, Shikano Kenshiro, Kondo Kunihiro, Taniuchi Shusuke, Furumitsu Megumi, Ochi Yuta, Sasaki Tsutomu, Okamoto Shiki, Bentley George E, Kriegsfeld Lance J, Minokoshi Yasuhiko, Ukena Kazuyoshi
Section of Behavioral Sciences, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, Japan.
Department of Integrative Biology and The Helen Wills Neuroscience Institute, University of California at Berkeley, Berkeley, United States.
Elife. 2017 Aug 11;6:e28527. doi: 10.7554/eLife.28527.
Mechanisms underlying the central regulation of food intake and fat accumulation are not fully understood. We found that neurosecretory protein GL (NPGL), a newly-identified neuropeptide, increased food intake and white adipose tissue (WAT) in rats. NPGL-precursor gene overexpression in the hypothalamus caused increases in food intake, WAT, body mass, and circulating insulin when fed a high calorie diet. Intracerebroventricular administration of NPGL induced de novo lipogenesis in WAT, increased insulin, and it selectively induced carbohydrate intake. Neutralizing antibody administration decreased the size of lipid droplets in WAT. mRNA expression was upregulated by fasting and low insulin levels. Additionally, NPGL-producing cells were responsive to insulin. These results point to NPGL as a novel neuronal regulator that drives food intake and fat deposition through de novo lipogenesis and acts to maintain steady-state fat level in concert with insulin. Dysregulation of NPGL may be a root cause of obesity.
食物摄入和脂肪积累的中枢调节机制尚未完全明确。我们发现,神经分泌蛋白GL(NPGL),一种新鉴定的神经肽,可增加大鼠的食物摄入量和白色脂肪组织(WAT)。下丘脑NPGL前体基因过表达会导致高热量饮食喂养的大鼠食物摄入量、WAT、体重和循环胰岛素增加。脑室内注射NPGL可诱导WAT中从头脂肪生成,增加胰岛素,并选择性诱导碳水化合物摄入。给予中和抗体可减小WAT中脂滴的大小。禁食和低胰岛素水平会上调mRNA表达。此外,产生NPGL的细胞对胰岛素有反应。这些结果表明,NPGL是一种新型神经元调节因子,通过从头脂肪生成驱动食物摄入和脂肪沉积,并与胰岛素协同作用以维持稳态脂肪水平。NPGL失调可能是肥胖的根本原因。