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首页> 外文期刊>BMC Complementary and Alternative Medicine >Gancao (Glycyrrhizae Radix) provides the main contribution to Shaoyao-Gancao decoction on enhancements of CYP3A4 and MDR1 expression via pregnane X receptor pathway in vitro
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Gancao (Glycyrrhizae Radix) provides the main contribution to Shaoyao-Gancao decoction on enhancements of CYP3A4 and MDR1 expression via pregnane X receptor pathway in vitro

机译:Gancao(Glycyrrhizae Radix)为芍药 - 甘草汤提供了对Cyp3A4和MDR1表达的增强,通过妊娠X受体途径在体外促进了主要贡献

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摘要

Chinese herbal formula Shaoyao Gancao decoction (SGD) is often used as an adjuvant with chemotherapeutic agents to treat cancer. Due to the herb-drug interactions, the alternations of drug metabolic enzyme and drug transporters induced by SGD deserve to be explored. We aimed to investigate the effect of SGD on the pregnane X receptor (PXR)-mediated transcriptional regulation of cytochrome P450 3A4 (CYP3A4) and drug transporter multidrug resistance protein 1 (MDR1) in vitro. Besides, we assessed the contribution of constituent herbs to SGD on the regulation of CYP3A4 and MDR1. The dual luciferase reporter gene system containing the hPXR expression plasmid and the reporter gene plasmid of CYP3A4 or MDR1 was co-transfected to HepG2 and Caco2 cells. Luciferase activities were determined using a Dual-luciferase reporter assay kit. The gene expression of CYP3A4 and MDR1 in the hPXR-transfected LS174T cells were assessed by real-time qPCR. Finally, the contribution of constituent herbs from SGD was evaluated. SGD, Shaoyao and Gancao concentration-dependently increased promoter activities of CYP3A4 and MDR1 in vitro. Moreover, SGD, Shaoyao and Gancao up-regulated CYP3A4 and MDR1 mRNA in hPXR-transfected LS174T cells. As the herbal constituent of SGD, Gancao possesses significantly higher levels of metabolic enzyme and drug transporters compared with Shaoyao. SGD tends to enhance CYP3A4 and MDR1 expression via PXR pathway, especially Gancao provides the main contribution. This study highlights a potential in vitro mechanism for SGD on the regulation of drug metabolic enzymes and drug transporters.
机译:中草原公式芍药汤(SGD)经常用作化学治疗剂治疗癌症的佐剂。由于草药相互作用,SGD诱导的药物代谢酶和药物转运蛋白的交替值得探索。我们旨在探讨SGD对体外细胞色素P450 3A4(CYP3A4)和药物转运蛋白多药抗性蛋白1(MDR1)的妊娠X受体(PXR)介导的转录调节的影响。此外,我们评估了组成草药对CYP3A4和MDR1的监管的贡献。含有HPXR表达质粒和CYP3A4或MDR1的报告基因质粒的双荧光素酶报告基因系统将与HepG2和CaCO 2细胞共转染。使用双荧光素酶报告试剂盒测定荧光素酶活性。通过实时QPCR评估HPXR转染的LS174T细胞中CYP3A4和MDR1的基因表达。最后,评估了来自SGD的组成草药的贡献。 SGD,绍洛和Gancao集中依赖性增加CYP3A4和MDR1的启动子活性。此外,在HPXR转染的LS174T细胞中,SGD,Shaoyao和Gancao上调CYP3A4和MDR1 mRNA。作为SGD的草药组分,与少岛相比,Gancao具有显着较高的代谢酶和药物转运蛋白水平。 SGD倾向于通过PXR途径增强CYP3A4和MDR1表达,特别是Gancao提供了主要贡献。本研究突出了SGD对药物代谢酶和药物转运蛋白调节的潜在体外机制。

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