In vitro inhibitory effects of herbal supplements on tamoxifen and irinotecan metabolism.

Fran Grappe, Gwen Nance, Lori Coward, Greg Gorman
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引用次数: 3

Abstract

Background: As the use of herbal supplements continues to rise throughout the world, the potential for drug-herbal interactions also increases. For chemotherapeutic prodrugs, this interaction could prevent the metabolic conversion of the prodrug to its active metabolite(s), thereby potentially resulting in subtherapeutic systemic exposure of the drug and reduced efficacy of the therapy.

Methods: In this study, in vitro metabolism with human liver microsomes is used to measure the impact of ten commonly used herbal supplements on the biotransformation of the chemotherapeutic prodrugs tamoxifen (TAM) and irinotecan (IR).

Results: Four of the herbals tested, echinacea, ginseng, lemon balm, and skullcap, were found to be strong inhibitors of the CYP450 enzymatic bioactivation pathways of TAM with IC50 values as percent of a single dose ranging from 0.019% to 0.34%. Two of the herbals, skullcap and lemon balm, were found to inhibit the carboxyesterase pathway of IR with values of 0.21 and 0.25, respectively.

Conclusions: Our data suggests that based on the measured IC50 values that skullcap and lemon balm could have potential negative clinical impact on the bioactivation of TAM but not likely with IR.

草药补充剂对他莫昔芬和伊立替康代谢的体外抑制作用。
背景:随着世界范围内草药补充剂的使用不断增加,药物-草药相互作用的可能性也在增加。对于化疗前药,这种相互作用可能会阻止前药向其活性代谢物的代谢转化,从而可能导致药物的亚治疗性全身暴露和治疗效果降低。方法:本研究采用人肝微粒体体外代谢法,测定10种常用草药补充剂对化疗前药他莫昔芬(TAM)和伊立替康(IR)生物转化的影响。结果:四种草药,紫锥菊,人参,柠檬香蜂草和黄顶草,被发现是TAM的CYP450酶生物活化途径的强抑制剂,单剂量的IC50值百分比在0.019%至0.34%之间。黄芩和柠檬香蜂草对IR的羧酶途径的抑制作用分别为0.21和0.25。结论:我们的数据表明,根据测量的IC50值,黄颅草和柠檬香蜂草可能对TAM的生物活性有潜在的负面临床影响,但对IR不太可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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