Disruption of type 3 adenylyl cyclase expression in the hypothalamus leads to obesity

H. Cao, Xuanmao Chen, Yimei Yang, D. Storm
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引用次数: 13

Abstract

Evidence from human studies and transgenic mice lacking the type 3 adenylyl cyclase (AC3) indicates that AC3 plays a role in the regulation of body weight. It is unknown in which brain region AC3 exerts such an effect. We examined the role of AC3 in the hypothalamus for body weight control using a floxed AC3 mouse strain. Here, we report that AC3 flox/flox mice became obese after the administration of AAV-CRE-GFP into the hypothalamus. Both male and female AC3 floxed mice showed heavier body weight than AAV-GFP injected control mice. Furthermore, mice with selective ablation of AC3 expression in the ventromedial hypothalamus also showed increased body weight and food consumption. Our results indicated that AC3 in the hypothalamus regulates energy balance.
下丘脑中3型腺苷酸环化酶表达的破坏导致肥胖
来自人类研究和缺乏3型腺苷酸环化酶(AC3)的转基因小鼠的证据表明,AC3在体重调节中起作用。目前尚不清楚AC3在哪个脑区发挥这种作用。我们使用一种粘接的AC3小鼠品系研究了AC3在下丘脑中控制体重的作用。在这里,我们报道了AAV-CRE-GFP进入下丘脑后,AC3 flox/flox小鼠变得肥胖。注射AAV-GFP的雄性和雌性AC3小鼠的体重均高于注射AAV-GFP的对照组小鼠。此外,选择性切除下丘脑腹内侧AC3表达的小鼠也显示出体重和食物消耗增加。我们的研究结果表明,下丘脑中的AC3调节能量平衡。
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