Andersson Karl-Erik
Department of Clinical and Experimental Pharmacology, Lund University Hospital, Lund, Sweden.
Scand J Urol Nephrol Suppl. 2004(215):54-7. doi: 10.1080/03008880410015192.
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.
刺激毒蕈碱受体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有所不同。一般来说,M1、M3和M5受体被认为优先与Gq/11偶联,激活磷酸肌醇水解,进而通过生成三磷酸肌醇导致细胞内钙的动员。M2和M4受体与百日咳毒素敏感的Gi/o偶联,导致腺苷酸环化酶活性受到抑制。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,毒蕈碱受体激活逼尿肌的主要途径可能是通过L型钙通道的钙内流,以及通过激活Rho激酶抑制肌球蛋白轻链磷酸酶,从而增加收缩机制对钙的敏感性。这些发现对排尿功能障碍治疗的重要性仍有待确定。