Kellermann G, Luyten-Kellermann M, Horning M, Stafford M
Drug Metab Dispos. 1975 Jan-Feb;3(1):47-50.
A high correlation was observed between the aryl hydrocarbon hydroxylase activities in short-term lymphocyte cultures of 23 individuals and their plasma half-lives of antipyrine and phenylbutazone. Individuals with low inducibility of aryl hydrocarbon hydroxylase activities had very long plasma half-lives of antipyrine and phenylbutazone, whereas subjects with high inducibility of aryl hydrocarbon hydroxylase activites had relatively short plasma half-lives. Individuals with intermediate aryl hydrocarbon hydroxylase activities displayed intermediate half-lives for both drugs. The observed correlation indicates determinants which are common to the elimination of antipyrine or phenylbutazone, and aryl hydrocarbon hydroxylase metabolism of hydrocarbons. The differences in rates of drug elimination are probably due to genetic differences and may have pharmacological and therapeutic significance.
在23名个体的短期淋巴细胞培养物中,芳烃羟化酶活性与其安替比林和保泰松的血浆半衰期之间观察到高度相关性。芳烃羟化酶活性诱导性低的个体,其安替比林和保泰松的血浆半衰期很长,而芳烃羟化酶活性诱导性高的受试者,其血浆半衰期相对较短。芳烃羟化酶活性中等的个体,这两种药物的半衰期也处于中等水平。观察到的这种相关性表明,安替比林或保泰松的消除以及烃类的芳烃羟化酶代谢存在共同的决定因素。药物消除速率的差异可能是由于基因差异,并且可能具有药理学和治疗学意义。