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氯普萘洛尔在犬、狒狒和猴体内的处置情况。

Disposition of pranolium chloride in dogs, baboons and monkeys.

作者信息

Allan L, Barrow A, Haskins N J, Rogers M, Rose D A, Palmer R F

出版信息

Eur J Drug Metab Pharmacokinet. 1981;6(3):179-87. doi: 10.1007/BF03189487.

Abstract

The general disposition of [14C]-Pranolium Chloride (SC-27761), a potential anti-arrhythmic agent, has been studied in the beagle dog, baboon and rhesus monkey. The compound was moderately absorbed from the gastro-intestinal tract of the three species at 5 mg/kg. There was appreciable inter-animal variation in the amount of absorption, and the absorption was dose-dependent in the monkey. After i.v. dosage the radioactivity was largely cleared via the kidneys. The initial elimination half-lives for Pranolium in the dog and primate were between 0.6 to 3.1 hours after i.v. dosage, but could not be determined after oral dosage. Less than 1% of the dose was localised in monkey fetal tissues, two hours after an i.v. dose was given to pregnant female rhesus monkeys, and the highest concentrations of radiolabel were detected in fetal liver. Pranolium was found to be extensively metabolised and 1-naphthol was identified as a major metabolite. Pranolium was excreted in urine both unchanged and as conjugates, but 1-naphthol was excreted largely as conjugates.

摘要

对一种潜在的抗心律失常药物[14C] - 氯普萘洛尔(SC - 27761)在比格犬、狒狒和恒河猴体内的总体处置情况进行了研究。该化合物以5mg/kg的剂量在这三种动物的胃肠道中吸收程度适中。动物个体间的吸收量存在明显差异,且在猴体内吸收呈剂量依赖性。静脉给药后,放射性物质主要通过肾脏清除。氯普萘洛尔在犬和灵长类动物体内静脉给药后的初始消除半衰期在0.6至3.1小时之间,但口服给药后无法确定。给怀孕的恒河猴静脉给药两小时后,剂量中不到1%的药物定位在猴胎儿组织中,且在胎儿肝脏中检测到最高浓度的放射性标记物。发现氯普萘洛尔被广泛代谢,1 - 萘酚被鉴定为主要代谢产物。氯普萘洛尔以原形和结合物形式经尿液排泄,但1 - 萘酚主要以结合物形式排泄。

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