Camus P, Coudert B, D'Athis P, Foucher P, Delchambre J, Dupront A, Jeannin L
Unit of Pulmonary Pharmacology and Toxicology, Université de Bourgogne, Dijon, France.
J Pharmacol Exp Ther. 1991 Dec;259(3):1247-55.
Nilutamide (N) is a potent antiandrogen used in the treatment of diffuse carcinoma of the prostate. The drug has been implicated in a few instances of pneumonitis in man. The present studies were carried out to examine N disposition in the isolated perfused lung (IPL) from rats. Both recirculating and single-pass IPL were used. Recirculation was run for 60 min at concentrations of N ranging between 12 and 120 microM (+1 mu Ci [14C]N). Single-pass perfusions were run for 30 min (uptake, 10 min; efflux, 20 min) at inflowing concentrations ranging from 12 to 480 microM (+1 mu Ci [14C]N). Nilutamide was concentrated in the recirculating IPL, and tissue to medium ratio (T/M) ranged between 6.6 and 4.2, depending on the inflowing concentration of N (Cin). High performance liquid chromatography analysis of extracts of 60-min lung homogenates demonstrated the primary amino metabolite of N in addition to the parent compound. This indicated reduction of the nitro moiety of N by lung tissues. At 60 min and Cin = 40 microM, 17.6 +/- 4.7% of the radioactivity present in lung was accounted for by the metabolite. Perfusate samples contained low to undetectable amounts of the metabolite. No metabolism of N was detected in single-pass IPL, possibly because of the shorter duration of experiments. Amount of N taken up in lung and T/M were similar to those found in recirculating preparations. Uptake of N in the single-pass IPL was proportional to N concentration up to 480 microM.(ABSTRACT TRUNCATED AT 250 WORDS)
尼鲁米特(N)是一种用于治疗前列腺弥漫性癌的强效抗雄激素药物。该药物在人类中曾有几例引发肺炎的情况。本研究旨在检测大鼠离体灌注肺(IPL)中尼鲁米特的处置情况。使用了再循环和单次灌注的IPL。再循环在尼鲁米特浓度为12至120微摩尔(+1微居里[14C]N)的条件下运行60分钟。单次灌注在流入浓度为12至480微摩尔(+1微居里[14C]N)的条件下运行30分钟(摄取10分钟;流出20分钟)。尼鲁米特在再循环的IPL中被浓缩,组织与培养基的比率(T/M)在6.6至4.2之间,这取决于尼鲁米特的流入浓度(Cin)。对60分钟肺匀浆提取物的高效液相色谱分析表明,除了母体化合物外,还有尼鲁米特的主要氨基代谢产物。这表明肺组织可使尼鲁米特的硝基部分还原。在60分钟且Cin = 40微摩尔时,肺中17.6 +/- 4.7%的放射性由该代谢产物构成。灌注液样本中该代谢产物的含量很低或无法检测到。在单次灌注的IPL中未检测到尼鲁米特的代谢,可能是因为实验持续时间较短。肺中尼鲁米特的摄取量和T/M与再循环制剂中的相似。在单次灌注的IPL中,尼鲁米特的摄取量与浓度成正比,直至480微摩尔。(摘要截断于250字)