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所选全身麻醉药对家兔某些抗心律失常药物药代动力学参数的影响。第三部分。普萘洛尔。

The influence of selected general anesthetics on pharmacokinetic parameters of some antiarrhythmic drugs in rabbits. Part III. Propranolol.

作者信息

Orszulak-Michalak D

机构信息

Department of Pharmacodynamics, Medical University of Lodz.

出版信息

Acta Pol Pharm. 1995 Jul-Aug;52(4):309-13.

PMID:8960259
Abstract

The influence of general anesthesia with thiopental (10 mg/kg), ketamine (4 mg/kg), or propofol (10 mg/kg) on the propranolol (0.3 mg/kg) pharmacokinetic parameters was studied in rabbits. It was established that during thiopental or propofol anesthesia the levels of propranolol were significantly higher than in control animals. The following main changes in propranolol pharmacokinetic parameters were found: 1) increase of the distribution rate constant during propofol anesthesia 2) prolonged biological half-life and mean residence time during thiopental or propofol anesthesia 3) increase of the area under drug level curve during thiopental or propofol anesthesia 4) decrease of systemic clearance and volume of distribution during thiopental or propofol anesthesia. The slightest influence on propranolol pharmacokinetics was exerted by ketamine anesthesia.

摘要

研究了硫喷妥钠(10毫克/千克)、氯胺酮(4毫克/千克)或丙泊酚(10毫克/千克)全身麻醉对家兔普萘洛尔(0.3毫克/千克)药代动力学参数的影响。结果表明,在硫喷妥钠或丙泊酚麻醉期间,普萘洛尔的血药浓度显著高于对照动物。发现普萘洛尔药代动力学参数有以下主要变化:1)丙泊酚麻醉期间分布速率常数增加;2)硫喷妥钠或丙泊酚麻醉期间生物半衰期和平均驻留时间延长;3)硫喷妥钠或丙泊酚麻醉期间药时曲线下面积增加;4)硫喷妥钠或丙泊酚麻醉期间全身清除率和分布容积降低。氯胺酮麻醉对普萘洛尔药代动力学的影响最小。

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