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细胞色素P450酶与帕金森病:迄今为止的情况

P450 enzymes and Parkinson's disease: the story so far.

作者信息

Riedl A G, Watts P M, Jenner P, Marsden C D

机构信息

Neurodegenerative Diseases Research Centre, Pharmacology Group, King's College, London, England.

出版信息

Mov Disord. 1998 Mar;13(2):212-20. doi: 10.1002/mds.870130204.

Abstract

Environmental or endogenous toxins may cause nigral cell death in Parkinson's disease (PD) as a result of genetic susceptibility conferred by altered expression of P450 enzymes. Attention over the last 10 years has focused on CYP2D6 polymorphisms and susceptibility to PD. This review summarizes reports arising from both phenotypic and genotypic studies involving CYP2D6 and PD. Phenotypic studies have failed to support a link between CYP2D6 and PD. The more powerful genetic studies initially indicated a link between CYP2D6B mutations and PD, but critical analysis of the literature and recent studies emerging from independent laboratories fail to confirm this. Mutations in CYP2D6B are also not implicated in familial PD. As yet, there is no conclusive evidence to suggest that CYP2D6 polymorphisms confer susceptibility to PD. Whether polymorphisms in other P450s (for example, CYP1A1 and CYP2E1) are implicated in PD remains to be established.

摘要

环境毒素或内源性毒素可能因P450酶表达改变所赋予的遗传易感性,导致帕金森病(PD)中的黑质细胞死亡。过去10年的研究重点集中在CYP2D6基因多态性与PD易感性上。这篇综述总结了涉及CYP2D6和PD的表型及基因型研究报告。表型研究未能支持CYP2D6与PD之间存在联系。更为有力的基因研究最初表明CYP2D6B突变与PD之间存在联系,但对文献的批判性分析以及独立实验室近期的研究未能证实这一点。CYP2D6B突变也与家族性PD无关。目前,尚无确凿证据表明CYP2D6基因多态性会使人易患PD。其他细胞色素P450(如CYP1A1和CYP2E1)的基因多态性是否与PD有关仍有待确定。

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