逼尿肌收缩——关注毒蕈碱受体。

Karl-Erik Andersson
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引用次数: 13

摘要

对毒蕈碱受体的刺激是动物和人类逼尿肌收缩激活的主要机制。毒蕈碱受体与g蛋白偶联,但信号转导系统可能不同。一般来说,M、M和M受体被认为优先与Gq/11偶联,激活磷酸肌苷水解,进而通过肌醇三磷酸生成动员细胞内钙。M2和M4受体偶联到百日咳毒素敏感的Gi/o,导致腺苷酸环化酶活性抑制。然而,在逼尿肌平滑肌中,可能涉及其他信号通路。最近的研究表明,逼尿肌毒碱受体激活的主要途径可能是钙通过l型钙通道内流,并通过激活rho激酶抑制肌球蛋白轻链磷酸酶,从而增加收缩机械对钙的敏感性。这些发现对治疗排尿功能障碍的重要性仍有待确定。
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Detrusor contraction--Focus on muscarinic receptors.

Stimulation of muscarinic receptors is a main mechanism for contractile activation of the detrusor from both animals and humans. Muscarinic receptors are coupled to G-proteins, but the signal transduction systems may vary. In general, M, M and M receptors are considered to couple preferentially to Gq/11, activating phosphoinositide hydrolysis, in turn leading to mobilization of intracellular calcium through inositol trisphosphate generation. M2 and M4 receptors couple to pertussis toxin-sensitive Gi/o, resulting in inhibition of adenylyl cyclase activity. However, in the detrusor smooth muscle, other signalling pathways may be involved. Recent investigations revealed that a main pathway for muscarinic receptor activation of the detrusor may be calcium influx via L-type calcium channels, and increased sensitivity to calcium of the contractile machinery via inhibition of myosin light chain phosphatase through activation of Rho-kinase. The importance of these findings for treatment of voiding dysfunction remains to be established.

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