Venkataramanan R, Axelson J E
J Pharmacol Exp Ther. 1980 Oct;215(1):235-9.
Studies were carried out to determine the susceptibility of tocainide disposition to the induction and inhibition of drug metabolizing enzymes by using the rat as an animal model. Pretreatment with phenobarbital resulted in a significant reduction in the area under the plasma concentration vs. time curve of tocainide administered i.v. An increase in clearance due to phenobarbital treatment was mainly accounted for by the increase in the disposition rate constant of tocainide. After p.o. or i.v. administration of tocainide, a significant reduction in the percentage of dose excreted as intact drug in the urine was observed in test animals. SKF 525A pretreatment resulted in impairment of the elimination of tocainide as reflected by a reduction in clearance mainly due to a decrease in the disposition rate constant. The inhibition of tocainide metabolism was apparent from the greater than 100% increase in the amount of intact drug excreted in the urine. The differential extent of inhibition of tocainide metabolism observed after a 15 and 20 mg/kg dose supports the involvement of metabolic processes in the nonlinear elimination kinetics of tocainide.
以大鼠作为动物模型进行了多项研究,以确定妥卡尼处置对药物代谢酶诱导和抑制的敏感性。用苯巴比妥预处理导致静脉注射妥卡尼后血浆浓度-时间曲线下面积显著降低。苯巴比妥治疗引起的清除率增加主要是由于妥卡尼处置速率常数的增加。口服或静脉注射妥卡尼后,在试验动物中观察到尿液中以原形药物排泄的剂量百分比显著降低。SKF 525A预处理导致妥卡尼清除率降低,主要是由于处置速率常数降低,反映出妥卡尼消除受损。尿液中排泄的原形药物量增加超过100%,表明妥卡尼代谢受到抑制。15和20mg/kg剂量后观察到的妥卡尼代谢抑制程度差异支持代谢过程参与妥卡尼的非线性消除动力学。