Woolhouse N M, Andoh B, Mahgoub A, Sloan T P, Idle J R, Smith R L
Clin Pharmacol Ther. 1979 Nov;26(5):584-91. doi: 10.1002/cpt1979265584.
The alicyclic and aromatic hydroxylation of debrisoquin was studied in Ghanaians. As in a previously studied Caucasian population, the alicyclic 4-hydroxylation of debrisoquin in Ghanaians was polymorphic. Three phenotypes were observed: homozygous extensive metabolizers (58%), heterozygous extensive metabolizers (36%), and homozygous poor metabolizers (6%). In contrast, British Caucasians are primarily monomorphic extensive metabolizers (92%) and homozygous poor metabolizers comprise 8% of the population. Urinary recovery of the drug and its hydroxylated metabolites was significantly less in the Ghanaian subjects. In both Ghanaian and British populations, aromatic hydroxylation producing 5-, 6-, 7-, and 8-hydroxydebrisoquin was shown to parallel the alicyclic 4-hydroxylation of debrisoquin, and thus to be controlled by the same gene locus. Debrisoquin is advocated as a tool for uncovering polymorphism in drug oxidation and its interethnic variations.
在加纳人中研究了去甲丙咪嗪的脂环族和芳香族羟基化作用。与先前研究的白种人群体一样,加纳人中去甲丙咪嗪的脂环族4-羟基化具有多态性。观察到三种表型:纯合子广泛代谢者(58%)、杂合子广泛代谢者(36%)和纯合子代谢不良者(6%)。相比之下,英国白种人主要是单态性广泛代谢者(92%),纯合子代谢不良者占该人群的8%。加纳受试者尿液中药物及其羟基化代谢产物的回收率显著较低。在加纳人和英国人群体中,产生5-、6-、7-和8-羟基去甲丙咪嗪的芳香族羟基化作用与去甲丙咪嗪的脂环族4-羟基化作用平行,因此受同一基因位点控制。去甲丙咪嗪被认为是揭示药物氧化多态性及其种族间差异的一种工具。