Devazepide increases food intake in male but not female Zucker rats

被引:10
作者
Strohmayer, AJ
Greenberg, D
机构
[1] CORNELL UNIV MED COLL, ROYAL N SHORE HOSP, DEPT NEUROL, NEW YORK, NY 10021 USA
[2] NEW YORK HOSP, CORNELL MED CTR, DEPT PSYCHIAT, NEW YORK, NY 10021 USA
[3] EW BOURNE BEHAV RES LAB, WHITE PLAINS, NY 10605 USA
关键词
sex differences; ingestion; CCK; gender; satiety; CCK antagonists; genetic obesity;
D O I
10.1016/0031-9384(96)83164-7
中图分类号
B84 [心理学];
学科分类号
04 ; 0402 ;
摘要
The genetically obese Zucker rat (fa/fa) is hyperphagic compared to lean controls (Fa/?). This hyperphagia is characterized by increased meal size. Cholecystokinin (CCK) has been shown to decrease meal size in many species including humans. In the present study we investigated the role of endogenous CCK in mediating the hyperphagia of male and female obese Zucker rats. CCKA-type receptors were blocked with the specific antagonist, devazepide, and test meal size was measured. Male obese and lean rats significantly increased food intake following devazepide. Neither obese nor lean female rats significantly increased food intake following devazepide. This is the first demonstration of a gender difference in endogenous CCK-mediated satiety. These results have implications for the higher incidence of eating disorders in females.
引用
收藏
页码:273 / 275
页数:3
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