Sirmans S M, Pieper J A, Lalonde R L, Smith D G, Self T H
Department of Clinical Pharmacy, University of Tennessee, Memphis.
Clin Pharmacol Ther. 1988 Jul;44(1):29-34. doi: 10.1038/clpt.1988.108.
Twelve healthy subjects received a single oral dose of theophylline, 5 mg/kg alone, and after 7 days of oral verapamil, 120 mg every 8 hours, diltiazem, 90 mg every 8 hours, and nifedipine, 20 mg every 8 hours, in randomized crossover fashion. Mean theophylline oral clearance decreased 18% and 12% after verapamil and diltiazem, respectively (p less than 0.05). No significant change in theophylline oral clearance was observed after nifedipine. Increases in mean theophylline half-life were observed after verapamil (10.8 +/- 3.2 hours) and diltiazem (9.9 +/- 2.4 hours) (p less than 0.05) but not after nifedipine (8.6 +/- 2.4 hours) when compared with control (8.6 +/- 1.9 hours). Apparent volume of distribution was unchanged. Urinary excretion data showed that the relative formation rate constants of 3-methylxanthine and 1,3-dimethyluric acid were decreased during verapamil and diltiazem (p less than 0.05) but not during nifedipine. No change in 1-methyluric acid excretion was observed. Increases in urinary elimination of unchanged theophylline were observed after verapamil, diltiazem, and nifedipine. The modest reduction in theophylline clearance observed after verapamil and diltiazem is not likely to produce clinically significant increases in theophylline concentrations in most patients.
12名健康受试者以随机交叉方式接受了单次口服剂量的茶碱(5mg/kg),单独服用,以及在口服维拉帕米(每8小时120mg)、地尔硫䓬(每8小时90mg)和硝苯地平(每8小时20mg)7天后服用。维拉帕米和地尔硫䓬给药后,茶碱的平均口服清除率分别下降了18%和12%(p<0.05)。硝苯地平给药后,未观察到茶碱口服清除率有显著变化。与对照组(8.6±1.9小时)相比,维拉帕米(10.8±3.2小时)和地尔硫䓬(9.9±2.4小时)给药后,茶碱的平均半衰期增加(p<0.05),但硝苯地平给药后未增加(8.6±2.4小时)。分布容积无变化。尿排泄数据显示,维拉帕米和地尔硫䓬给药期间,3-甲基黄嘌呤和1,3-二甲基尿酸的相对生成速率常数降低(p<0.05),但硝苯地平给药期间未降低。未观察到1-甲基尿酸排泄的变化。维拉帕米、地尔硫䓬和硝苯地平给药后,未变化的茶碱的尿排泄增加。维拉帕米和地尔硫䓬给药后观察到的茶碱清除率的适度降低,在大多数患者中不太可能导致茶碱浓度出现具有临床意义的升高。