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棕色脂肪组织质膜中的调控机制。

Control mechanisms in brown adipose tissue plasma membrane.

作者信息

Bégin-Heick N, Heick H M

出版信息

Can J Biochem Cell Biol. 1984 Jul;62(7):631-6. doi: 10.1139/o84-084.

Abstract

It is generally agreed that the site of heat production during nonshivering thermogenesis is the brown adipose tissue (BAT) and that the triggering event for heat production is the interaction of noradrenaline (NA) with its receptor on the plasma membrane. Following this initial event, several changes occur which result in increased rates of cAMP synthesis, redistribution of ions across the membrane, enhanced rates of lipolysis, and increased mitochondrial oxidation of substrates. BAT is also a target for the anabolic effect of insulin. Available evidence shows that insulin receptors are present on the BAT plasma membrane and that insulin can oppose the metabolic effects of catecholamine on BAT. We have studied more particularly the response of BAT adenylate cyclase to catecholamines in an animal model (the ob/ob mouse) which has a defective thermogenic response. The capacity of adenylate cyclase to be stimulated by catecholamines was significantly less in the tissue of obese mice than in lean controls. To produce a response equal to the half-maximal response in the lean mouse, a 10-fold increase in the NA concentration was required in the BAT of the obese mouse. These results are in harmony with those of others showing that the lipolytic response to catecholamines is abnormal in the BAT of the obese mouse. The adenylate cyclase activity can be altered by changes in the lipid composition of the diet and by manipulation of hormone levels. It is likely that the alteration in adenylate cyclase responsiveness is one of the contributing factors in the impaired thermogenesis and obesity in this animal.

摘要

一般认为,非寒战性产热的产热部位是棕色脂肪组织(BAT),产热的触发事件是去甲肾上腺素(NA)与其质膜上的受体相互作用。在这一初始事件之后,会发生一些变化,导致环磷酸腺苷(cAMP)合成速率增加、离子跨膜重新分布、脂肪分解速率提高以及线粒体底物氧化增加。BAT也是胰岛素合成代谢作用的靶点。现有证据表明,BAT质膜上存在胰岛素受体,胰岛素可以对抗儿茶酚胺对BAT的代谢作用。我们更具体地研究了在一种产热反应有缺陷的动物模型(ob/ob小鼠)中,BAT腺苷酸环化酶对儿茶酚胺的反应。肥胖小鼠组织中腺苷酸环化酶受儿茶酚胺刺激的能力明显低于瘦对照组。为了在肥胖小鼠的BAT中产生与瘦小鼠中半最大反应相等的反应,需要将NA浓度提高10倍。这些结果与其他研究结果一致,表明肥胖小鼠的BAT中对儿茶酚胺的脂解反应异常。饮食中脂质成分的变化和激素水平的调控可以改变腺苷酸环化酶的活性。腺苷酸环化酶反应性的改变很可能是这种动物产热受损和肥胖的促成因素之一。

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