2 Receptor mechanisms and their role in drug interactions: effects of anaesthetics on G-protein-activated intracellular signalling pathways

Md, PhD R.H. Henning (Assistant Professor of Pharmacology), Md, PhD Anne H. Epema (Consultant Anaesthetist)
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引用次数: 0

Abstract

Different types of receptor-mediated mechanism play a key role in cellular transmembrane communication. The majority of plasma membrane receptors mediate the effects of neurotransmitters and hormones through activation of GTP-binding proteins (G-proteins). Coupling of the activated receptor to a G-protein initiates (occasionally inhibits) a cascade of enzyme-catalysed reactions leading to the production of one or more second messengers, eventually leading to the physiological response. The most commonly known cascades are the phosphoinositide and the cAMP route. This paper will describe the key concepts of G-protein-mediated signalling of both cascades and introduce the concept of ‘cross-talk’. Further, the effects of anaesthetics on the intracellular components of these signalling pathways will be reviewed.

受体机制及其在药物相互作用中的作用:麻醉对g蛋白激活的细胞内信号通路的影响
不同类型的受体介导机制在细胞跨膜通讯中起着关键作用。大多数质膜受体通过激活gtp结合蛋白(g蛋白)介导神经递质和激素的作用。激活受体与g蛋白的偶联启动(偶尔抑制)一系列酶催化反应,导致一个或多个第二信使的产生,最终导致生理反应。最常见的级联是磷酸肌苷和cAMP途径。本文将描述两个级联中g蛋白介导的信号传导的关键概念,并介绍“串扰”的概念。此外,麻醉药对这些信号通路的细胞内成分的影响将被回顾。
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