Skin Reactions Associated to Phenytoin Administration: Multifactorial Cause

M. Vázquez, P. Fagiolino, Silvana Alvariza, M. Ibarra, Cecilia Maldonado, R. González, A. Laborde, M. Uría, A. Carozzi, C. Azambuja
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引用次数: 5

Abstract

Purpose: Cutaneous reactions can be associated with phenytoin administration. Such reactions can be explained by the formation of reactive species (arene oxide and quinones) capable of interacting covalently with cell macromolecules during phenytoin metabolism. Enzymes involved in reactive species detoxification are polimorphically expressed in humans. A genetic abnormality leading to a defective microsomal epoxidase hydrolase (main detoxification enzyme) activity could be one of the causes leading to this kind of adverse effect, but not the only one. The purpose of this study was to give a deeper insight into the main causes leading to skin reactions. Methods: Cutaneous reactions experienced by some healthy volunteers enrolled in a pharmacokinetic study of phenytoin were analyzed in depth. The activity of the microsomal epoxidase enzyme was determined. Results: Six out of twelve healthy volunteers receiving phenytoin in multiple doses exhibited rash. More female subjects or volunteers with a rapid input of the drug and/or a faster phenytoin metabolism or defective microsomal epoxidase hydrolase activity experienced these cutaneous reactions. Conclusions: Arene oxide metabolite seems to be the responsible entity for cutaneous reactions. The genesis of this adverse effect after phenytoin administration is multifactorial revealing that other risks factors (not only the genetic one) such as being a woman in the fertile life period or under contraceptive therapy, or a rapid drug input and /or a faster phenytoin metabolism could lead to a higher formation rate of the arene oxide.
与苯妥英相关的皮肤反应:多因素原因
目的:皮肤反应可能与苯妥英给药有关。这种反应可以解释为在苯妥英代谢过程中能够与细胞大分子共价相互作用的活性物质(氧化芳烃和醌)的形成。参与活性物种解毒的酶在人类中是多态表达的。遗传异常导致微粒体环氧酶水解酶(主要解毒酶)活性缺陷可能是导致这种不良反应的原因之一,但不是唯一的原因。这项研究的目的是为了更深入地了解导致皮肤反应的主要原因。方法:对一些参加苯妥英药代动力学研究的健康志愿者的皮肤反应进行深入分析。测定微粒体环氧化酶活性。结果:12名接受多剂量苯妥英的健康志愿者中有6人出现皮疹。更多的女性受试者或志愿者快速输入药物和/或更快的苯托英代谢或有缺陷的微粒体环氧化酶水解酶活性经历这些皮肤反应。结论:氧化芳烃代谢物可能是皮肤反应的主要原因。苯妥英给药后这种不良反应的成因是多因素的,揭示了其他风险因素(不仅仅是遗传因素),如处于生育期或正在接受避孕治疗的女性,或快速的药物输入和/或更快的苯妥英代谢可能导致芳烃氧化物的形成率更高。
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