Desager J P, Harvengt C, Bianchetti G, Rosenzweig P
Laboratoire de Pharmacothérapie, Université Catholique de Louvain, Faculty of Medicine, Brussels, Belgium.
Int J Clin Pharmacol Ther Toxicol. 1993 Nov;31(11):568-71.
Alfuzosin is a new alpha 1-adrenoceptor antagonist particularly effective in the symptomatic treatment of benign prostatic hypertrophy (BPH). The elimination of alfuzosin being almost entirely metabolic, the potential pharmacokinetic interaction with cimetidine (H2-receptor antagonist) was investigated in 10 healthy young subjects. Pharmacokinetics of alfuzosin were appraised as a 5 mg oral dose before, after one day and after 20 days of cimetidine (1 g/d) administration. An inhibition of the hepatic mixed function oxidase system by cimetidine was established by the oral antipyrine clearance test. Under these conditions, alfuzosin pharmacokinetics were only marginally affected by concomitant cimetidine administration. Surprisingly, a significantly shorter elimination half-life was found after 20 days on cimetidine (from 5.1 +/- 0.4 h to 4.4 +/- 0.5 h). This fact must be attributed to the large inter-individual variation in pharmacokinetic parameters reported for alfuzosin. Cmax and AUC increased up to 20% after cimetidine but without statistical significance. No side-effects on the association cimetidine-alfuzosin were reported. In conclusion, there is a lack of pharmacokinetic interaction on cimetidine-alfuzosin co-administration.
阿夫唑嗪是一种新型α1肾上腺素能受体拮抗剂,对良性前列腺增生(BPH)的症状治疗特别有效。由于阿夫唑嗪几乎完全通过代谢消除,因此在10名健康年轻受试者中研究了其与西咪替丁(H2受体拮抗剂)潜在的药代动力学相互作用。在给予西咪替丁(1g/天)之前、给药一天后和给药20天后,评估5mg口服剂量阿夫唑嗪的药代动力学。通过口服安替比林清除试验确定西咪替丁对肝混合功能氧化酶系统的抑制作用。在这些条件下,同时给予西咪替丁对阿夫唑嗪的药代动力学仅有轻微影响。令人惊讶的是,服用西咪替丁20天后发现消除半衰期明显缩短(从5.1±0.4小时降至4.4±0.5小时)。这一事实必须归因于所报道的阿夫唑嗪药代动力学参数存在较大的个体间差异。西咪替丁给药后,Cmax和AUC增加高达20%,但无统计学意义。未报道西咪替丁与阿夫唑嗪联用的副作用。总之,西咪替丁与阿夫唑嗪联用不存在药代动力学相互作用。