Donnelly R, Elliott H L, Meredith P A, Howie C A, Reid J L
University Department of Medicine and Therapeutics, Gardiner Institute, Western Infirmary, Glasgow, UK.
Eur J Clin Pharmacol. 1993;44(3):279-82. doi: 10.1007/BF00271372.
In a single-blind study 12 normotensive men took nifedipine 20 mg (Group 1, n = 6) or doxazosin 2 mg (Group 2, n = 6), followed by the combination. Each subject attended on four 9-h study days for evaluation of the effects of single and multiple doses of the monotherapy and the effects of adding single and multiple doses of the second drug. Measurements of BP, HR, plasma drug concentrations, and apparent liver blood flow were recorded. The combination was generally well tolerated. BP was consistently lower with the combination than with either monotherapy: for example, average erect BP was 108/61 (Group 1) and 112/62 mmHg (Group 2) compared with 122/66 and 116/68 during steady-state monotherapy. The introduction of nifedipine in Group 2 was associated with a significant increase in liver blood flow at 1.5 h: 1560 vs 1050 ml.min-1 during monotherapy with doxazosin. There was no significant kinetic interaction. In particular, the steady-state AUC of doxazosin was unaffected by the addition of nifedipine: 257, 307, 301, and 256 ng.ml-1.h for the 4 study days (Group 2).
在一项单盲研究中,12名血压正常的男性服用硝苯地平20毫克(第1组,n = 6)或多沙唑嗪2毫克(第2组,n = 6),随后服用联合药物。每位受试者参加4个为期9小时的研究日,以评估单药治疗的单剂量和多剂量效果以及添加单剂量和多剂量第二种药物的效果。记录血压、心率、血浆药物浓度和表观肝血流量的测量值。联合用药总体耐受性良好。联合用药时的血压始终低于单药治疗时:例如,平均直立血压在第1组为108/61,在第2组为112/62 mmHg,而在稳态单药治疗期间分别为122/66和116/68。在第2组中引入硝苯地平与1.5小时时肝血流量显著增加有关:多沙唑嗪单药治疗期间为1050 ml.min-1,联合用药时为1560 ml.min-1。没有显著的动力学相互作用。特别是,多沙唑嗪的稳态AUC不受添加硝苯地平的影响:第2组4个研究日分别为257、307、301和256 ng.ml-1.h。