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Novel plant inducers of PXR-dependent cytochrome P450 3A4 expression in HepG2 cells

机译:新型植物诱导剂诱导HepG2细胞表达PXR依赖性细胞色素P450 3A4

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摘要

The cytochrome P450 3A4 (CYP3A4) is the most abundant CYP450 enzyme involved in the metabolism of endogenous products and xenobiotics, including prescription drugs and herbals. Modulation of hepatic CYP3A4 gene expression via nuclear receptors, like pregnane X receptor (PXR), is a major cause of adverse effects like drug-unresponsiveness and toxicity. In the present study, ethanol extracts of 58 medicinal plants, belonging to 27 families, were evaluated for potential activities in CYP3A4 induction in HepG2 cells by reporter gene assay. For PXR-mediated CYP3A4 induction, a 50 μg/ml concentration was used for all non-cytotoxic plants extracts. Rifampicin (10 μM) and DMSO (0.1%) were used as standard inducer and untreated (negative) control, respectively. The comparative fold-induction of CYP34A by the plant extracts in relation to the untreated control was determined. As a result, Dodonaea angustifolia (2.62 fold; P < 0.0001) was found to be the most promising inducer of CYP3A4, followed by Euphorbia tirucalli (1.95 fold; P = 0.0004), Alternanthera pungens (1.74 fold, P = 0.0035), and Ficus palmata (1.65 fold; P = 0.0097). Further phytochemical characterizations of the active plants are therefore, warranted.
机译:细胞色素P450 3A4(CYP3A4)是参与内源性产品和异源生物(包括处方药和草药)代谢的最丰富的CYP450酶。通过核受体(如孕烷X受体(PXR))对肝CYP3A4基因表达的调节是药物不良反应和毒性等不良反应的主要原因。在本研究中,通过报告基因分析评估了属于27个科的58种药用植物的乙醇提取物在HepG2细胞中CYP3A4诱导中的潜在活性。对于PXR介导的CYP3A4诱导,所有非细胞毒性植物提取物均使用50μg/ ml的浓度。利福平(10μm)和DMSO(0.1%)分别用作标准诱导剂和未处理(阴性)对照。相对于未处理的对照,确定了植物提取物对CYP34A的相对诱导的折叠。结果发现,Dodonaea angustifolia(2.62倍; P <0.0001)是CYP3A4最有希望的诱导剂,其次是大戟Euphorbia tirucalli(1.95倍; P = 0.0004),Alternanthera pungens(1.74倍,P = 0.0035),和掌状榕(1.65倍; P = 0.0097)。因此,需要对活性植物进行进一步的植物化学表征。

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