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下尿路中的毒蕈碱受体亚型。

Muscarinic receptor subtypes in the lower urinary tract.

作者信息

Giglio Daniel, Tobin Gunnar

机构信息

Department of Pharmacology, Institute of Neuroscience and Physiology, Sahlgrenska Academy at University of Gothenburg, Gothenburg, Sweden.

出版信息

Pharmacology. 2009;83(5):259-69. doi: 10.1159/000209255. Epub 2009 Mar 19.

Abstract

Acetylcholine acting on muscarinic M(3) receptors on the detrusor muscle is the principal stimulus for inducing the contractile response for urinary bladder voiding. The urinary bladder expresses, however, all cloned muscarinic receptor subtypes (M(1)-M(5)). In terms of quantity, the M(2) subtype dominates over the M(3) subtype in the detrusor, and its role in contraction seems to be primarily indirect, by blocking stimuli from cAMP-coupled receptors that induce relaxation. The excitatory M(1) and inhibitory M(2) and/or M(4) subtypes are also expressed prejunctionally. Muscarinic M(1) and M(2)/M(4) autoreceptors facilitate and inhibit, respectively, the release of acetylcholine. The urothelium had been considered to be a passive barrier; however, during the last decade, it has been shown that the urothelium is of importance for bladder function. In a state of bladder pathology, muscarinic receptor changes occur in the detrusor, prejunctionally, and in the urothelium, but the character of the change differs between disorders. The urothelium expresses all subtypes of muscarinic receptors, and upon stimulation it releases factors affecting bladder afferents and smooth muscle. During inflammation, the expression of muscarinic M(5) receptors is increased, particularly in the urothelium, together with a cholinergic-induced production of nitric oxide in the mucosa. The present review describes signalling mechanisms, expression and functional effects of muscarinic receptors in the lower urinary tract. Their roles in physiological and pathophysiological conditions, as well as clinical implications of the occurrence of different muscarinic receptors, are discussed.

摘要

乙酰胆碱作用于逼尿肌上的毒蕈碱型M(3)受体是诱导膀胱排尿收缩反应的主要刺激因素。然而,膀胱表达所有已克隆的毒蕈碱型受体亚型(M(1)-M(5))。就数量而言,M(2)亚型在逼尿肌中占主导地位,超过M(3)亚型,其在收缩中的作用似乎主要是间接的,通过阻断来自诱导舒张的cAMP偶联受体的刺激。兴奋性M(1)和抑制性M(2)和/或M(4)亚型也在神经节前表达。毒蕈碱型M(1)和M(2)/M(4)自身受体分别促进和抑制乙酰胆碱的释放。尿路上皮曾被认为是一个被动屏障;然而,在过去十年中,已表明尿路上皮对膀胱功能很重要。在膀胱病理状态下,毒蕈碱型受体在逼尿肌、神经节前和尿路上皮中发生变化,但不同疾病之间变化的特征不同。尿路上皮表达所有毒蕈碱型受体亚型,受到刺激时会释放影响膀胱传入神经和平滑肌的因子。在炎症期间,毒蕈碱型M(5)受体的表达增加,特别是在尿路上皮中,同时黏膜中会有胆碱能诱导的一氧化氮产生。本综述描述了毒蕈碱型受体在下尿路中的信号传导机制、表达和功能作用。讨论了它们在生理和病理生理条件下的作用,以及不同毒蕈碱型受体出现的临床意义。

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