Muscarinic Receptors in Cardioprotection and Vascular Tone Regulation.

IF 1.9 4区 医学 Q3 PHYSIOLOGY
E Dolejší, A Janoušková, J Jakubík
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引用次数: 0

Abstract

Muscarinic acetylcholine receptors are metabotropic G-protein coupled receptors. Muscarinic receptors in the cardiovascular system play a central role in its regulation. Particularly M2 receptors slow down the heart rate by reducing the impulse conductivity through the atrioventricular node. In general, activation of muscarinic receptors has sedative effects on the cardiovascular system, including vasodilation, negative chronotropic and inotropic effects on the heart, and cardioprotective effects, including antifibrillatory effects. First, we review the signaling of individual subtypes of muscarinic receptors and their involvement in the physiology and pathology of the cardiovascular system. Then we review age and disease-related changes in signaling via muscarinic receptors in the cardiovascular system. Finally, we review molecular mechanisms involved in cardioprotection mediated by muscarinic receptors leading to negative chronotropic and inotropic and antifibrillatory effects on heart and vasodilation, like activation of acetylcholine-gated inward-rectifier K+-currents and endothelium-dependent and -independent vasodilation. We relate this knowledge with well-established cardioprotective treatments by vagal stimulation and muscarinic agonists. It is well known that estrogen exerts cardioprotective effects against atherosclerosis and ischemia-reperfusion injury. Recently, some sex hormones and neurosteroids have been shown to allosterically modulate muscarinic receptors. Thus, we outline possible treatment by steroid-based positive allosteric modulators of acetylcholine as a novel pharmacotherapeutic tactic. Keywords: Muscarinic receptors, Muscarinic agonists, Allosteric modulation, Cardiovascular system, Cardioprotection, Steroids.

心肌保护和血管张力调节中的毒蕈碱受体
肌卡因乙酰胆碱受体是一种代谢性 G 蛋白偶联受体。心血管系统中的毒蕈碱受体在心血管系统的调节中发挥着核心作用。尤其是 M2 受体,它通过降低通过房室结的冲动传导性来减慢心率。一般来说,激活毒蕈碱受体会对心血管系统产生镇静作用,包括扩张血管、对心脏产生负向时动力和肌力作用,以及心脏保护作用,包括抗颤作用。首先,我们回顾了毒蕈碱受体各个亚型的信号传导及其在心血管系统生理和病理中的参与。然后,我们回顾了心血管系统中毒蕈碱受体信号传递中与年龄和疾病相关的变化。最后,我们回顾了由毒蕈碱受体介导的心脏保护的分子机制,这些机制导致对心脏和血管舒张的负性促时差作用、肌力作用和抗纤颤作用,如激活乙酰胆碱门控的向内整流 K+ 电流以及内皮依赖性和非依赖性血管舒张。我们将这一知识与通过迷走神经刺激和毒蕈碱激动剂进行的成熟的心脏保护治疗联系起来。众所周知,雌激素对动脉粥样硬化和缺血再灌注损伤具有心脏保护作用。最近,一些性激素和神经类固醇被证明可对毒蕈碱受体进行异构调节。因此,我们概述了以类固醇为基础的乙酰胆碱正性异构调节剂作为一种新型药物治疗策略的可能性。关键词毒蕈碱受体 毒蕈碱激动剂 异构调节 心血管系统 保护心脏 类固醇
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来源期刊
Physiological research
Physiological research 医学-生理学
CiteScore
4.00
自引率
4.80%
发文量
108
审稿时长
3 months
期刊介绍: Physiological Research is a peer reviewed Open Access journal that publishes articles on normal and pathological physiology, biochemistry, biophysics, and pharmacology. Authors can submit original, previously unpublished research articles, review articles, rapid or short communications. Instructions for Authors - Respect the instructions carefully when submitting your manuscript. Submitted manuscripts or revised manuscripts that do not follow these Instructions will not be included into the peer-review process. The articles are available in full versions as pdf files beginning with volume 40, 1991. The journal publishes the online Ahead of Print /Pre-Press version of the articles that are searchable in Medline and can be cited.
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