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肥胖啮齿动物模型中心脏腺苷酸环化酶活性的调节

Regulation of cardiac adenylate cyclase activity in rodent models of obesity.

作者信息

Strassheim D, Houslay M D, Milligan G

机构信息

Department of Biochemistry, University of Glasgow, Scotland, U.K.

出版信息

Biochem J. 1992 Apr 1;283 ( Pt 1)(Pt 1):203-8. doi: 10.1042/bj2830203.

Abstract

We have investigated beta-adrenergic regulation of adenylate cyclase activity in heart tissue membranes from the genetically obese Zucker rat, the genetically obese CBA mouse and the genetically obese diabetic (db/db) mouse. Responsiveness to beta-adrenergic stimulation was impaired in membranes from the obese Zucker rat, but not in the other models. The membranes from obese Zucker rats showed both decreased beta-adrenergic-receptor number and altered coupling between beta-adrenergic receptors and the stimulatory guanine-nucleotide-binding protein, Gs. In contrast, no alterations in either the levels of Gs or the functional interaction between this protein and the catalytic moiety of adenylate cyclase were observed. In these three genetic models of obesity we observe dissimilar alterations in the control of adenylate cyclase.

摘要

我们研究了遗传性肥胖的 Zucker 大鼠、遗传性肥胖的 CBA 小鼠和遗传性肥胖糖尿病(db/db)小鼠心脏组织膜中腺苷酸环化酶活性的β-肾上腺素能调节。肥胖 Zucker 大鼠的膜对β-肾上腺素能刺激的反应性受损,但在其他模型中未受损。肥胖 Zucker 大鼠的膜显示β-肾上腺素能受体数量减少,且β-肾上腺素能受体与刺激性鸟嘌呤核苷酸结合蛋白 Gs 之间的偶联发生改变。相比之下,未观察到 Gs 水平或该蛋白与腺苷酸环化酶催化部分之间功能相互作用的改变。在这三种肥胖遗传模型中,我们观察到腺苷酸环化酶控制方面存在不同的改变。

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J Hered. 1950 Dec;41(12):317-8. doi: 10.1093/oxfordjournals.jhered.a106073.
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