Badawi Jasmin Katrin, Li Heng, Langbein Sigrun, Kwon Sun-Tscheol, Kamp Stefan, Bross Stephan
Department of Urology, University Hospital Mannheim, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Eur J Clin Pharmacol. 2006 May;62(5):347-54. doi: 10.1007/s00228-006-0100-8. Epub 2006 Apr 7.
The inhibitory and relaxant effects of the L-type calcium antagonists nifedipine, nimodipine, verapamil and diltiazem, and of the T-type calcium antagonist mibefradil, on contractions of isolated human detrusor muscle were investigated. The tissue was obtained from 10 patients undergoing cystectomy due to bladder cancer. Effects of the calcium antagonists at different concentrations on the concentration-response curves for carbachol were investigated. Furthermore, concentration-relaxation curves were performed using potassium-precontracted muscle strips. All L-type calcium antagonists suppressed the mean concentration-response curve of carbachol significantly at a concentration of 10(-6) M. Mibefradil up to 10(-5) M did not significantly suppress it. Nifedipine significantly reduced the carbachol-induced maximum contraction to 75% and 44%, verapamil to 75% and 67% of the appropriate control value at concentrations of 10(-7) and 10(-6) M, respectively. Diltiazem reduced it insignificantly to 96% and 71% at the above-mentioned concentrations. The concentration-relaxation experiments revealed following pD2-values and maximum relaxations of nifedipine, nimodipine, verapamil and diltiazem, respectively: 6.23, 6.37, 5.66, 5.81 and 85%, 83%, 82%, 90%. Maximum relaxations and pD2-values were not significantly different from each other. The lowest concentration, for which a significant effect compared to control in Student;s t-test was found, amounted to 10(-10) M, 10(-9) M, 10(-7) M, 10(-6.5) M and 10(-4) M for nimodipine, nifedipine, diltiazem, verapamil and mibefradil, respectively. L-type calcium antagonists are very potent relaxant agents of the human detrusor muscle in vitro.
研究了L型钙拮抗剂硝苯地平、尼莫地平、维拉帕米和地尔硫䓬以及T型钙拮抗剂米贝拉地尔对离体人逼尿肌收缩的抑制和松弛作用。组织取自10例因膀胱癌接受膀胱切除术的患者。研究了不同浓度的钙拮抗剂对卡巴胆碱浓度-反应曲线的影响。此外,使用钾预收缩的肌肉条进行浓度-松弛曲线实验。所有L型钙拮抗剂在浓度为10(-6) M时均显著抑制卡巴胆碱的平均浓度-反应曲线。米贝拉地尔在浓度高达10(-5) M时未显著抑制该曲线。硝苯地平在浓度分别为10(-7) 和10(-6) M时,将卡巴胆碱诱导的最大收缩显著降低至相应对照值的75%和44%,维拉帕米则分别降低至75%和67%。地尔硫䓬在上述浓度下将其无显著降低至96%和71%。浓度-松弛实验分别显示硝苯地平、尼莫地平、维拉帕米和地尔硫䓬的以下pD2值和最大松弛率:6.23、6.37、5.66、5.81和85%、83%、82%、90%。最大松弛率和pD2值彼此之间无显著差异。在学生t检验中与对照相比发现有显著作用的最低浓度,尼莫地平、硝苯地平、地尔硫䓬、维拉帕米和米贝拉地尔分别为10(-10) M、10(-9) M、10(-7) M、10(-6.5) M和10(-4) M。L型钙拮抗剂在体外是人体逼尿肌非常有效的松弛剂。