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Safety of Herbal Medicinal Products: Echinacea and Selected Alkylamides Do Not Induce CYP3A4 mRNA Expression

机译:草药产品的安全性:紫锥菊和某些烷基酰胺不诱导CYP3A4 mRNA表达

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摘要

A major safety concern with the use of herbal medicinal products (HMP) is their interactions with conventional medicines, which are often mediated via the cytochrome P450 (CYP) system. Echinacea is a widely used over-the-counter HMP, with proven immunomodulatory properties. Its increasing use makes research into its safety an urgent concern. Previously, we showed that Echinacea extracts and its alkylamides (thought to be important for Echinacea's immunomodulatory activity) mildly inhibit the enzymatic activity of the main drug metabolising CYP isoforms, but to this date, there is insufficient work on its ability to alter CYP expression levels. We now report for the first time the effect of a commercial Echinacea extract (Echinaforce) and four Echinacea alkylamides on the transcription of the major drug metabolizing enzyme CYP3A4. HepG2 cells were exposed for 96 h to clinically relevant concentrations of Echinaforce (22, 11.6 and 1.16 μg mL−1) or the alkylamides (1.62 and 44 nM). CYP3A4 mRNA levels were quantified using real-time reverse transcription polymerase chain reaction (RT-PCR). Neither Echinaforce nor the alkylamides produced any significant changes in the steady-state CYP3A4 mRNA levels, under these conditions. In contrast, treatment with 50 μM rifampicin resulted in a 3.8-fold up-regulation over the vehicle control. We conclude that Echinaforce is unlikely to affect CYP3A4 transcriptional levels, even at concentrations which can inhibit the enzymatic activity of CYP3A4. Overall, our data provides further evidence for the lack of interactions between Echinacea and conventional drugs.
机译:使用草药产品(HMP)的主要安全问题是它们与常规药物的相互作用,这些相互作用通常是通过细胞色素P450(CYP)系统介导的。紫锥菊是一种广泛使用的非处方HMP,具有成熟的免疫调节特性。它的越来越多的使用使对其安全性的研究成为迫切关注的问题。以前,我们表明紫锥菊提取物及其烷基酰胺(对紫锥菊的免疫调节活性很重要)可轻度抑制主要药物代谢CYP亚型的酶促活性,但迄今为止,对其改变CYP表达水平的能力尚无足够的研究。 。现在,我们首次报道商业紫锥菊提取物(Echinaforce)和四种紫锥菊烷基酰胺对主要药物代谢酶CYP3A4转录的影响。将HepG2细胞暴露于临床相关浓度的Echinaforce(22、11.6和1.16μgmL-1)或烷基酰胺(1.62和44 nM)中96小时。使用实时逆转录聚合酶链反应(RT-PCR)对CYP3A4 mRNA水平进行定量。在这些条件下,Echinaforce和烷基酰胺均未在稳态CYP3A4 mRNA水平上产生任何显着变化。相比之下,用50μm的利福平进行处理会导致载体对照上调3.8倍。我们得出的结论是,Echinaforce不太可能影响CYP3A4的转录水平,即使浓度可以抑制CYP3A4的酶促活性。总体而言,我们的数据为紫锥菊与传统药物之间缺乏相互作用提供了进一步的证据。

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