Mice With Hyperghrelinemia Are Hyperphagic and Glucose Intolerant and Have Reduced Leptin Sensitivity

被引:54
作者
Bewick, Gavin A. [1 ]
Kent, Aysha [1 ]
Campbell, Daniel [1 ]
Patterson, Michael [1 ]
Ghatei, Mohammed A. [1 ]
Bloom, Stephen R. [1 ]
Gardiner, James V. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Invest Med, London, England
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
CENTRALLY ADMINISTERED GHRELIN; HORMONE SECRETAGOGUE RECEPTOR; BROWN ADIPOSE-TISSUE; ARCUATE NUCLEUS; ENDOGENOUS GHRELIN; PANCREATIC-ISLETS; GH SECRETAGOGUE; TRANSGENIC MICE; ENERGY-BALANCE; FOOD-INTAKE;
D O I
10.2337/db08-1428
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE-Ghrelin is the only known peripheral hormone to increase ingestive behavior. However, its role in the physiological regulation of energy homeostasis is unclear because deletion of ghrelin or its receptor does not alter food intake or body weight in mice fed a normal chow diet. We hypothesized that overexpression of ghrelin in its physiological tissues would increase food intake and body weight. RESEARCH DESIGN AND METHODS-We used bacterial artificial chromosome transgenesis to generate a mouse model with increased ghrelin expression and production in the stomach and brain. We investigated the effect of ghrelin overexpression on food intake and body weight. We also measured energy expenditure and determined glucose tolerance, glucose stimulated insulin release, and peripheral insulin sensitivity. RESULTS-Ghrelin transgenic (Tg) mice exhibited increased circulating bioactive ghrelin, which was associated with hyperphagia, increased energy expenditure, glucose intolerance, decreased glucose stimulated insulin secretion, and reduced leptin sensitivity. CONCLUSIONS-This is the first report of a Tg approach suggesting that ghrelin regulates appetite under normal feeding conditions and provides evidence that ghrelin plays a fundamental role in regulating beta-cell function. Diabetes 58:840-846, 2009
引用
收藏
页码:840 / 846
页数:7
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