Mahgoub A, Idle J R, Dring L G, Lancaster R, Smith R L
Lancet. 1977 Sep 17;2(8038):584-6. doi: 10.1016/s0140-6736(77)91430-1.
Debrisoquine and its primary metabolite, 4-hydroxydebrisoquine, were measured in the urine of 94 volunteers after a single oral dose of 10 mg debrisoquine. The ratio between excreted debrisoquine and its metabolite was bimorphically distributed in the study population. Family studies supported the view that alicyclic 4-hydroxylation of debrisoquine is controlled by a single autosomal gene and that a defect in this metabolic step is caused by a recessive allele.
在94名志愿者单次口服10毫克异喹胍后,检测了他们尿液中的异喹胍及其主要代谢产物4-羟基异喹胍。在研究人群中,排泄的异喹胍与其代谢产物的比例呈双态分布。家系研究支持以下观点:异喹胍的脂环族4-羟基化由单个常染色体基因控制,且该代谢步骤中的缺陷由隐性等位基因引起。