Peart Jason N, Gross Garrett J
Department of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
Drug News Perspect. 2005 May;18(4):237-42. doi: 10.1358/dnp.2005.18.4.908657.
Opioid and adenosine receptors are implicated in numerous physiological and pathophysiological states. Moreover, both G-protein-coupled receptor families have been demonstrated to provide significant protection against ischemic injury in the myocardium and central nervous system (CNS). Much recent data report a tight interaction between these two receptor families, from alterations in receptor sensitivity to release of endogenous adenosine in the presence of morphine. Indeed, it appears that the cardioprotective effects of adenosine can be abolished by opioid receptor antagonists and vice-versa. This review aims to highlight some of the research, derived from both the CNS and myocardium, supporting this interesting interaction.
阿片类受体和腺苷受体与多种生理和病理生理状态有关。此外,这两个G蛋白偶联受体家族均已被证明能为心肌和中枢神经系统(CNS)的缺血性损伤提供显著保护。最近有许多数据报道了这两个受体家族之间的紧密相互作用,从受体敏感性的改变到吗啡存在时内源性腺苷的释放。事实上,腺苷的心脏保护作用似乎可被阿片受体拮抗剂消除,反之亦然。本综述旨在强调一些来自中枢神经系统和心肌的研究,以支持这种有趣的相互作用。