Shaw P N, Houston J B, Rowland M, Hopkins K, Thiercelin J F, Morselli P L
Br J Clin Pharmacol. 1985 Dec;20(6):611-8. doi: 10.1111/j.1365-2125.1985.tb05119.x.
Antipyrine total clearance and the formation clearance of its major metabolites were studied in normal, healthy male volunteers before and after multiple dosing for approximately three weeks with phenytoin (six subjects) and carbamazepine (six subjects). Total antipyrine clearance increased on average by 91% after phenytoin dosing and by 61% after carbamazepine and individual increases correlated well with mean plasma concentrations of the anti-epileptic drug. The increase in total clearance resulted largely from increased formation clearances of the 4-hydroxy and 3-hydroxymethylantipyrine metabolites with minimal effect on the norantipyrine pathway, following treatment with both enzyme-inducing drugs. It is concluded that both phenytoin and carbamazepine have similar effects on antipyrine metabolism and that these effects are mediated by induction of specific forms of cytochrome P450.
在正常健康男性志愿者中,研究了苯妥英(6名受试者)和卡马西平(6名受试者)多次给药约三周前后安替比林的总清除率及其主要代谢产物的生成清除率。苯妥英给药后,安替比林总清除率平均增加91%,卡马西平给药后增加61%,个体清除率的增加与抗癫痫药物的平均血浆浓度密切相关。两种酶诱导药物治疗后,总清除率的增加主要是由于4-羟基安替比林和3-羟甲基安替比林代谢产物的生成清除率增加,对去甲安替比林途径影响最小。结论是苯妥英和卡马西平对安替比林代谢有相似作用,且这些作用是由细胞色素P450特定形式的诱导介导的。