Truss M C, Uckert S, Stief C G, Kuczyk M, Schulz-Knappe P, Forssmann W G, Jonas U
Department of Urology, Hannover Medical School, Germany.
Neurourol Urodyn. 1996;15(1):59-70. doi: 10.1002/(SICI)1520-6777(1996)15:1<59::AID-NAU6>3.0.CO;2-E.
The cyclic nucleotides cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) are second messengers involved in the regulation of contractility in various smooth muscle organs including detrusor smooth muscle. They are synthesized by activation of adenylate and guanylate cyclases, respectively, and inactivated by phosphodiesterases (PDEs). In order to delineate the intracellular regulation of porcine detrusor contractility by cyclic nucleotides and phosphodiesterases, functional organ bath studies and determinations of intracellular cyclic nucleotide contents were performed after incubation of porcine detrusor strips with forskolin (adenylate cyclase activator), sodium nitroprusside (guanylate cyclase activator), and various phosphodiesterase-inhibitors. Significant relaxant responses were achieved only by forskolin, the nonspecific phosphodiesterase-inhibitor papaverine, and the phosphodiesterase 1-inhibitor vinpocetine (62.4 +/- 5.6%, 73 +/- 4.3%, and 53 +/- 7.9%, respectively). Sodium nitroprusside and the selective PDE-inhibitors milrinone, rolipram, zaprinast, and dipyridamole were significantly less efficacious (26.9 +/- 3.9%, 15.5 +/- 3.8%, 15.3 +/- 3.0%, 13 +/- 4.0%, and 13.2 +/- 2.1%, respectively). Forskolin, papaverine, and vinpocetine elevated intracellular cAMP concentrations (7.3-, 1.9-, and 1.7-fold increase at 100 microM, respectively), whereas the other substances failed to enhance cAMP levels. cGMP levels were only increased by sodium nitroprusside (7.8-fold). The adenylate cyclase-cAMP system seems to be the more important signal transduction system involved in the relaxation of carbachol induced smooth muscle tone of the porcine detrusor. The role of the guanylate cyclase-cGMP system is less clear. In addition, the calcium/calmodulin-stimulated PDE I seems to be of major functional importance in regulating cAMP hydrolysis in the porcine detrusor smooth muscle in vitro.
环核苷酸环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)是参与调节包括逼尿肌平滑肌在内的各种平滑肌器官收缩性的第二信使。它们分别通过腺苷酸环化酶和鸟苷酸环化酶的激活而合成,并被磷酸二酯酶(PDEs)灭活。为了阐明环核苷酸和磷酸二酯酶对猪逼尿肌收缩性的细胞内调节作用,在用福斯可林(腺苷酸环化酶激活剂)、硝普钠(鸟苷酸环化酶激活剂)和各种磷酸二酯酶抑制剂孵育猪逼尿肌条后,进行了功能性器官浴研究和细胞内环核苷酸含量的测定。仅福斯可林、非特异性磷酸二酯酶抑制剂罂粟碱和磷酸二酯酶1抑制剂长春西汀能产生显著的舒张反应(分别为62.4±5.6%、73±4.3%和53±7.9%)。硝普钠以及选择性PDE抑制剂米力农、咯利普兰、扎普司特和双嘧达莫的效果明显较差(分别为26.9±3.9%、15.5±3.8%、15.3±3.0%、13±4.0%和13.2±2.1%)。福斯可林、罂粟碱和长春西汀提高了细胞内cAMP浓度(在100微摩尔时分别增加7.3倍、1.9倍和1.7倍),而其他物质未能提高cAMP水平。cGMP水平仅被硝普钠提高(7.8倍)。腺苷酸环化酶 - cAMP系统似乎是参与猪逼尿肌卡巴胆碱诱导的平滑肌张力舒张的更重要信号转导系统。鸟苷酸环化酶 - cGMP系统的作用尚不清楚。此外,钙/钙调蛋白刺激的PDE I似乎在体外调节猪逼尿肌平滑肌中cAMP水解方面具有主要功能重要性。