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Role of Cytochrome P4502B6 Polymorphisms in Ketamine Metabolism and Clearance

机译:细胞色素P4502B6基因多态性在氯胺酮代谢和清除中的作用。

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Background: At therapeutic concentrations, cytochrome P4502B6 (CYP2B6) is the major P450 isoform catalyzing hepatic ketamine N-demethylation to norketamine in vitro. The CYP2B6 gene is highly polymorphic. The most common variant allele, CYP2B6*6, is associated with diminished hepatic CYP2B6 expression and catalytic activity compared with wild-type CYP2B6*1/*1. CYP2B6.6, the protein encoded by the CYP2B6*6 allele, and liver microsomes from CYP2B6*6 carriers had diminished ketamine metabolism in vitro. This investigation tested whether humans with the CYP2B6*6 allele would have decreased clinical ketamine metabolism and clearance.
机译:背景:在治疗浓度下,细胞色素P4502B6(CYP2B6)是体外催化肝脏氯胺酮N-去甲基化为正氯胺酮的主要P450亚型。 CYP2B6基因是高度多态的。与野生型CYP2B6 * 1 / * 1相比,最常见的变异等位基因CYP2B6 * 6与肝脏CYP2B6的表达和催化活性降低有关。 CYP2B6 * 6等位基因编码的蛋白质CYP2B6.6和CYP2B6 * 6携带者的肝微粒体在体外减少了氯胺酮的代谢。这项研究测试了具有CYP2B6 * 6等位基因的人是否会降低临床氯胺酮的代谢和清除率。

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