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肾上腺素能和毒蕈碱受体调节及其在心力衰竭中的治疗意义

Adrenergic and muscarinic receptor regulation and therapeutic implications in heart failure.

作者信息

Schmitz W, Boknik P, Linck B, Müller F U

机构信息

Institut für Pharmakologie und Toxikologie, Westfälische Wilhelms-Universität, Münster, Germany.

出版信息

Mol Cell Biochem. 1996;157(1-2):251-8. doi: 10.1007/BF00227907.

Abstract

In end-stage heart failure the expression of different myocardial regulatory proteins involved in the beta-adrenergic cAMP signalling pathway is altered. The downregulation of beta 1-adrenoceptors and their uncoupling from the effector as well as an increased expression of the inhibitory GTP-binding protein seem to be the most important alterations. Since catecholamine levels are elevated in these patients and since some alterations can be 'restored' after treatment with beta-adrenoceptor antagonists it was hypothesized that excessive beta-adrenergic stimulation could be involved in these alterations. In this article the changes of beta-adrenergic receptors, GTP-binding proteins, sarcoplasmic reticulum Ca(2+)-ATPase and of phospholamban found in heart failure are addressed with its possible therapeutic implications.

摘要

在终末期心力衰竭中,参与β-肾上腺素能环磷酸腺苷(cAMP)信号通路的不同心肌调节蛋白的表达会发生改变。β1-肾上腺素能受体的下调及其与效应器的解偶联,以及抑制性GTP结合蛋白表达的增加似乎是最重要的改变。由于这些患者体内儿茶酚胺水平升高,且一些改变在用β-肾上腺素能受体拮抗剂治疗后可“恢复”,因此推测过度的β-肾上腺素能刺激可能与这些改变有关。本文探讨了心力衰竭时β-肾上腺素能受体、GTP结合蛋白、肌浆网Ca(2+)-ATP酶和受磷蛋白的变化及其可能的治疗意义。

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