Nesfatin-1: An Overview and Future Clinical Application

被引:101
作者
Shimizu, Hiroyuki [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; Food intake; Body weight; Obesity; BLOOD-BRAIN-BARRIER; SATIETY MOLECULE; NEURONS; IDENTIFICATION; GHRELIN; HORMONE; LEPTIN;
D O I
10.1507/endocrj.K09E-117
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nesfatin/nucleobindin 2 (NUCB2) is expressed in the appetite-control hypothalamic nuclei and brainstem nuclei. Nesfatin/NUCB2 expression in the paraventricular nucleus of the hypothalamus was modulated by starvation and refeeding. Intracerebroventricular administration of nesfatin-1 dose-dependently inhibited food intake for 6 hours in male Wistar and leptin resistant, Zucker fatty rats. Intraperitoneal administration of nesfatin-1 and its mid-segment (M30) dose-dependently inhibited food intake for 3 hours in male ICR mice. Intraperitoncal administration of M30 also decreased food intake in leptin-resistant, genetically obese (ob/ob), diabetic (db/db) mice and mice fed a 45% high fat diet for 28 days. Intraperitoneal administration of M30 increased proopiomelanocortin and cocaine- and amphetamine- related peptide mRNA expression in the nucleus of the solitary tract of mice. In addition, intranasal administration of nesfatin-1 significantly inhibited food intake for 6 hours in male Wistar rats. We summarize recent observations about nesfatin-1, and attempt to present future direction of nesfatin-1 research for developing a new anti-obesity treatment.
引用
收藏
页码:537 / 543
页数:7
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