The effect of cimetidine on the pharmacokinetics of single oral doses of alfuzosin.

J P Desager, C Harvengt, G Bianchetti, P Rosenzweig
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Abstract

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.

西咪替丁对单次口服阿呋唑嗪药代动力学的影响。
Alfuzosin是一种新型的α 1-肾上腺素受体拮抗剂,对良性前列腺肥大(BPH)的对症治疗特别有效。在10名健康青年受试者中,alfuzosin几乎完全代谢消除,研究了其与西咪替丁(h2受体拮抗剂)的潜在药代动力学相互作用。分别在西咪替丁(1 g/d)给药前、给药1 d后和给药20 d后,以5 mg口服剂量评价阿呋唑嗪的药代动力学。通过口服安替林清除率试验,建立了西咪替丁对肝脏混合功能氧化酶系统的抑制作用。在这些条件下,阿呋唑嗪的药代动力学仅受伴随给药西咪替丁的轻微影响。令人惊讶的是,服用西咪替丁20天后,消除半衰期明显缩短(从5.1 +/- 0.4 h降至4.4 +/- 0.5 h)。这一事实必须归因于阿夫唑嗪的药代动力学参数在个体间的巨大差异。Cmax和AUC在西咪替丁治疗后可提高20%,但无统计学意义。西咪替丁-阿夫唑嗪联合用药无副作用报道。综上所述,西咪替丁与阿呋唑嗪合用缺乏药代动力学相互作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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