A new anorexigenic protein, nesfatin-1

被引:95
作者
Shimizu, Hiroyuki [1 ]
Ohsaki, Aya [1 ]
Oh-I, Sinsuke [1 ]
Okada, Shuichi [1 ]
Mori, Masatomo [1 ]
机构
[1] Gunma Univ, Grad Sch Med, Dept Med & Mol Sci, Maebashi, Gunma 3718511, Japan
关键词
Nesfatin-1; Leptin; Melanocortin; Food intake; Body weight; BLOOD-BRAIN-BARRIER; SATIETY MOLECULE; VAGAL NERVE; FOOD-INTAKE; NEURONS; MECHANISMS; GHRELIN; HORMONE;
D O I
10.1016/j.peptides.2009.01.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
An anorexigenic peptide, nesfatin-1 was found in rat hypothalamus, and its expression in the paraventricular nucleus of the hypothalamus was reduced by starvation. Intracerebroventricular administration dose-dependently inhibited food intake for 6 h in male Wistar and leptin resistant, Zucker fatty rats. There may be a crosstalk between nesfatin-1 pathway and melanocortin pathway in the brain. Nesfatin-1 neurons co-express with oxytocin, vasopressin and melanin concentrating hormone in the hypothalamus. Intraperitoneal administration of nesfatin-1 and its mid-segment dose-dependently inhibited food intake for 3 h. Mid-segment of nesfatin-1 decreased food intake under leptin-resistant animal models of obesity. Intraperitoneal administration of the mid-segment of nesfatin-1 increased proopiomelanocortin and cocain- and amphetamine-related peptide mRNA expression in the nucleus of the solitary tract, but not in arcuate nucleus of the hypothalamus. In this review, we summarized recent progress in the research about the possible mechanism of nesfatin-1-induced anorexia. (C) 2009 Published by Elsevier Inc.
引用
收藏
页码:995 / 998
页数:4
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