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地伐西匹可增加雄性但不增加雌性 Zucker 大鼠的食物摄入量。

Devazepide increases food intake in male but not female Zucker rats.

作者信息

Strohmayer A J, Greenberg D

机构信息

Department of Neurology, North Shore University Hospital-Cornell University Medical College, NY, USA.

出版信息

Physiol Behav. 1996 Jul;60(1):273-5. doi: 10.1016/0031-9384(96)83164-7.

Abstract

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.

摘要

与瘦的对照大鼠(Fa/?)相比,遗传性肥胖的 Zucker 大鼠(fa/fa)食量过大。这种食量过大的特征是每餐食量增加。胆囊收缩素(CCK)已被证明在包括人类在内的许多物种中可减少每餐食量。在本研究中,我们调查了内源性 CCK 在介导雄性和雌性肥胖 Zucker 大鼠食量过大方面的作用。使用特异性拮抗剂地伐西匹阻断 CCKA 型受体,并测量试餐量。给予地伐西匹后,雄性肥胖和瘦大鼠的食物摄入量显著增加。给予地伐西匹后,肥胖和瘦的雌性大鼠的食物摄入量均未显著增加。这是内源性 CCK 介导的饱腹感存在性别差异的首次证明。这些结果对女性饮食失调发病率较高具有启示意义。

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