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基因肥胖小鼠(ob/ob)脂肪细胞质膜中腺苷酸环化酶对肾上腺素刺激的反应受损。

An impaired response of adenylate cyclase to stimulation by epinephrine in adipocyte plasma membranes from genetically obese mice (ob/ob).

作者信息

Laudat M H, Pairault J

出版信息

Eur J Biochem. 1975 Aug 15;56(2):583-9. doi: 10.1111/j.1432-1033.1975.tb02265.x.

Abstract

The present studies have established that there is an impaired response to epinephrine of the adenylate system in adipocyte preparations from obese hyperglycemic mice as compared to their thin littermates. In contrast, membrane preparations from both groups of animals were found to exhibit a similar response to fluoride ion. The response of adenylate cyclase to epinephrine was enhanced to a similar extent by increasing the ATP concentration in adipocyte plasma membranes from the two groups of animals. While GTP (0.1 muM) elicited an ATP-like response of similar magnitude in adenylate cyclase activity in both membrane preparations, it did not therefore abolish the impaired response to epinephrine of adenylate cyclase activity in membranes of obese mice. The response of adenylate cyclase activity to (--)-epinephrine in membrane preparations from obese mice progressively diminished with the age of these animals. In contrast, the concentration of (--)-epinephrine required for half-maximal stimulation of adenylate cyclase was similar and remained unchanged with the age for both membrane preparations. These data suggest that a perturbation may occur in the coupling step between the hormone receptor and the catalytic site of the adenylate cyclase system in obese mice. While a 15-day restrictive diet or a 72-h period of fasting was found to normalize the hyperinsulinemia of obese animals, neither affected the response of adenylate cyclase to epinephrine in preparations of adipocyte membranes from these mice. These results suggest that the observed defect in the response of plasma membrane adenylate cyclase activity to epinephrine in obese mice does not result from their hyperinsulinism.

摘要

目前的研究已证实,与瘦的同窝小鼠相比,肥胖高血糖小鼠脂肪细胞制剂中腺苷酸系统对肾上腺素的反应受损。相比之下,发现两组动物的膜制剂对氟离子表现出相似的反应。通过增加两组动物脂肪细胞质膜中的ATP浓度,腺苷酸环化酶对肾上腺素的反应增强到相似程度。虽然GTP(0.1μM)在两种膜制剂的腺苷酸环化酶活性中引发了类似大小的ATP样反应,但它并没有消除肥胖小鼠膜中腺苷酸环化酶活性对肾上腺素的受损反应。肥胖小鼠膜制剂中腺苷酸环化酶活性对(-)-肾上腺素的反应随着这些动物年龄的增长而逐渐减弱。相比之下,半最大刺激腺苷酸环化酶所需的(-)-肾上腺素浓度相似,并且两种膜制剂的该浓度随年龄保持不变。这些数据表明,肥胖小鼠的激素受体与腺苷酸环化酶系统催化位点之间的偶联步骤可能发生紊乱。虽然发现15天的限制性饮食或72小时的禁食可使肥胖动物的高胰岛素血症正常化,但两者均未影响这些小鼠脂肪细胞膜制剂中腺苷酸环化酶对肾上腺素的反应。这些结果表明,肥胖小鼠中观察到的质膜腺苷酸环化酶活性对肾上腺素反应的缺陷并非由其高胰岛素血症所致。

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