肾上腺素能受体与脂肪组织代谢和产热的控制。

Sheila Collins, R. Surwit
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引用次数: 246

摘要

-肾上腺素能受体(β -肾上腺素能受体)是G蛋白偶联受体大家族的成员。有三种β - aar亚型(β - 1ar, β - 2ar和β - 3ar),每一种都与Galphas偶联并刺激细胞内cAMP水平。beta1AR和beta2AR在机体各组织中广泛表达,而beta3AR主要存在于脂肪细胞中。β受体的刺激导致白色脂肪细胞的脂肪分解和棕色脂肪的非寒战产热。然而,基本上在所有的肥胖动物模型中,β - aar系统功能失调,刺激脂肪分解和产热的能力受损。然而,我们和其他人已经证明,选择性β 3ar激动剂能够预防或逆转肥胖和β 3ar表达的丧失,并刺激产热。本章将回顾目前对交感神经系统和脂肪细胞β - ars在肥胖模型中的作用的理解;β - aar表达变化对机体组成和产热的生理影响;以及褐色和白色脂肪细胞中β - aar亚型的调节和独特特性。后者包括我们最近发现的β 3ar利用新的信号转导机制同时激活蛋白激酶A和MAP激酶途径。了解这些途径的影响及其在调节适应性产热中的潜在作用进行了讨论。
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The beta-adrenergic receptors and the control of adipose tissue metabolism and thermogenesis.
The beta-adrenergic receptors (betaARs) are members of the large family of G protein-coupled receptors. There are three betaAR subtypes (beta1AR, beta2AR beta3AR), each of which is coupled to Galphas and the stimulation of intracellular cAMP levels. While beta1AR and beta2AR are broadly expressed throughout tissues of the body, beta3AR is found predominantly in adipocytes. Stimulation of the betaARs leads to lipolysis in white adipocytes and nonshivering thermogenesis in brown fat. However, in essentially all animal models of obesity, the betaAR system is dysfunctional and the ability to stimulate lipolysis and thermogenesis is impaired. Nevertheless, we and others have shown that selective beta3AR agonists are able to prevent or reverse obesity and the loss of betaAR expression and to stimulate thermogenesis. This chapter will review the current understanding of the role of the sympathetic nervous system and the adipocyte betaARs in models of obesity; the physiologic impact of changes in betaAR expression on body composition and thermogenesis; and the regulation and unique properties of betaAR subtypes in brown and white adipocytes. The latter includes our recent discovery of novel signal transduction mechanisms utilized by beta3AR to activate simultaneously the protein kinase A and MAP kinase pathways. The impact of understanding these pathways and their potential role in modulating adaptive thermogenesis is discussed.
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