Orszulak-Michalak D
Department of Pharmacodynamics, Faculty of Pharmacy, School of Medicine, Lódź.
Acta Pol Pharm. 1995 Mar-Apr;52(2):147-51.
The influence of general anesthesia with thiopental (10 mg/kg), ketamine (4 mg/kg), propofol (10 mg/kg) or pentobarbital (20 mg/kg) on the N-acetylprocainamide (15 mg/kg) pharmacokinetic parameters was studied in rabbits. It was established that during thiopental or pentobarbital anesthesia the levels of N-acetylprocainamide may be temporary higher than therapeutic levels. The following main changes in N-acetylprocainamide pharmacokinetic parameters were found: 1) increase of the elimination rate and shortening of biological half-life during thiopental or ketamine anesthesia 2) decrease of mean residence time during thiopental anesthesia 3) increase of the elimination rate from the central compartment constant (but not the mean residence time) during pentobarbital anesthesia 4) decrease of distribution rate and penetration rates (k12, k21) during propofol anesthesia.
研究了硫喷妥钠(10毫克/千克)、氯胺酮(4毫克/千克)、丙泊酚(10毫克/千克)或戊巴比妥(20毫克/千克)全身麻醉对家兔N - 乙酰普鲁卡因胺(15毫克/千克)药代动力学参数的影响。结果表明,在硫喷妥钠或戊巴比妥麻醉期间,N - 乙酰普鲁卡因胺的血药浓度可能暂时高于治疗水平。发现N - 乙酰普鲁卡因胺药代动力学参数有以下主要变化:1)硫喷妥钠或氯胺酮麻醉期间消除速率增加,生物半衰期缩短;2)硫喷妥钠麻醉期间平均驻留时间缩短;3)戊巴比妥麻醉期间中央室消除速率常数增加(但平均驻留时间未增加);4)丙泊酚麻醉期间分布速率和通透速率(k12、k21)降低。