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戊巴比妥对阿普洛尔处置的影响。

Effect of pentobarbital on the disposition of alprenolol.

作者信息

Alván G, Piafsky K, Lind M, von Bahr C

出版信息

Clin Pharmacol Ther. 1977 Sep;22(3):316-21. doi: 10.1002/cpt1977223316.

Abstract

Alprenolol was administered orally and intravenously to 5 healthy subjects before and after 10 to 14 daily doses of 0.1 gm pentobarbital. The area under the plasma concentration time curve after an oral 200-mg dose decreased from 706 +/- 277 to 154 +/- 48 ng/ml-hr (mean and SD) with the barbiturate treatment, but there was no significant change in elimination rate. The change in area corresponded to an increase in extraction by the liver from 0.72 +/- 0.13 to 0.93 +/- 0.01. The disposition of a 5.0-mg intravenous dose of alprenolol did not change significantly after pentobarbital treatment. There was no indication of a marked change in hepatic blood flow estimated from the clearance of alprenolol after intravenous administration. It is concluded that pentobarbital administration induces the metabolism of alprenolol in man and that the pharmacokinetic theories derived for hepatic extraction of drugs subject to a high metabolic clearance can be successfully applied.

摘要

在5名健康受试者每日服用10至14剂0.1克戊巴比妥之前和之后,分别口服和静脉注射阿普洛尔。服用巴比妥类药物后,口服200毫克剂量后的血浆浓度-时间曲线下面积从706±277降至154±48纳克/毫升·小时(平均值和标准差),但消除率无显著变化。面积的变化对应于肝脏提取率从0.72±0.13增加到0.93±0.01。戊巴比妥治疗后,静脉注射5.0毫克阿普洛尔的处置情况无显著变化。根据静脉注射后阿普洛尔的清除率估算的肝血流量没有明显变化迹象。得出的结论是,服用戊巴比妥可诱导人体中阿普洛尔的代谢,并且为高代谢清除率药物的肝脏提取推导的药代动力学理论可以成功应用。

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