首页> 外文期刊>British Journal of Clinical Pharmacology >Influence of the CYP2D6*10 allele on the metabolism of mexiletine by human liver microsomes.
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Influence of the CYP2D6*10 allele on the metabolism of mexiletine by human liver microsomes.

机译:CYP2D6 * 10等位基因对人肝微粒体代谢美西律的影响。

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AIMS: To study the influence of CYP2D6*10 on the formation of p-hydroxymexiletine (PHM) and hydroxymethylmexiletine (HMM) using microsomes from human liver of known genotypes. METHODS: Microsomes from human livers of genotype CYP2D6*1/*1 (n = 5), *1/*10 (n = 6) and *10/*10 (n = 6) were used in this study. The formation of PHM and HMM was determined by high-performance liquid chromatography. RESULTS: The formation rates of PHM and HMM were decreased by more than 50% and 85% in CYP2D6*1/*10 and *10/*10 microsomes, respectively, compared with *1/*1 microsomes. CONCLUSIONS: The metabolism of mexiletine to form PHM and HMM appears to be impaired to a significant extent in human liver microsomes from hetero- and homozygotes of CYP2D6*10.
机译:目的:使用已知基因型人肝微粒体,研究CYP2D6 * 10对p-羟美西汀(PHM)和羟甲基美西汀(HMM)形成的影响。方法:本研究使用来自人类肝脏的CYP2D6 * 1 / * 1(n = 5),* 1 / * 10(n = 6)和* 10 / * 10(n = 6)基因型微粒体。通过高效液相色谱法确定PHM和HMM的形成。结果:与* 1 / * 1微粒体相比,CYP2D6 * 1 / * 10和* 10 / * 10微粒体的PHM和HMM形成率分别降低了50%和85%以上。结论在人肝微粒体中,CYP2D6 * 10杂合子和纯合子对美西律的代谢形成PHM和HMM的作用似乎受到很大程度的损害。

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