Department of Pharmacology, Toxicology and Therapeutics, University of Kansas Medical Center, Kansas City, KS 66160, USA.
Drug Metab Dispos. 2010 Dec;38(12):2226-31. doi: 10.1124/dmd.110.035253. Epub 2010 Aug 24.
Sophora flavescens (SF) is an herbal medicine widely used for the treatment of viral hepatitis, cancer, viral myocarditis, gastrointestinal hemorrhage, and skin diseases. It was recently reported that SF up-regulates CYP3A expression. The mechanism of SF-induced CYP3A expression is unknown. In the current study, we tested the hypothesis that SF-induced CYP3A expression is mediated by the activation of pregnane X receptor (PXR). We used two cell lines, DPX2 and HepaRG, to investigate the role of PXR in SF-induced CYP3A expression. The DPX2 cell line is derived from HepG2 cells with the stable transfection of human PXR and a luciferase reporter gene linked with a human PXR response element identified in the CYP3A4 gene promoter. In DPX2 cells, SF activated PXR in a concentration-dependent manner. We used a metabolomic approach to identify the chemical constituents in SF, which were further analyzed for their effect on PXR activation and CYP3A regulation. One chemical in SF, N-methylcytisine, was identified as an individual chemical that activated PXR. HepaRG is a highly differentiated hepatoma cell line that mimics human hepatocytes. In HepaRG cells, N-methylcytisine significantly induced CYP3A4 expression, and this induction was suppressed by the PXR antagonist sulforaphane. These results suggest that SF induces CYP3A expression via the activation of PXR.
苦参(SF)是一种草药,广泛用于治疗病毒性肝炎、癌症、病毒性心肌炎、胃肠道出血和皮肤病。最近有报道称,SF 可上调 CYP3A 的表达。SF 诱导 CYP3A 表达的机制尚不清楚。在本研究中,我们检验了 SF 通过激活孕烷 X 受体(PXR)诱导 CYP3A 表达的假说。我们使用了两个细胞系,DPX2 和 HepaRG,来研究 PXR 在 SF 诱导 CYP3A 表达中的作用。DPX2 细胞系源自 HepG2 细胞,通过稳定转染人 PXR 和人 CYP3A4 基因启动子中鉴定的人 PXR 反应元件的荧光素酶报告基因构建而成。在 DPX2 细胞中,SF 以浓度依赖性方式激活 PXR。我们采用代谢组学方法鉴定 SF 中的化学物质,并进一步分析它们对 PXR 激活和 CYP3A 调节的影响。SF 中的一种化学物质,N-甲基胞嘧啶,被鉴定为一种可单独激活 PXR 的化学物质。HepaRG 是一种高度分化的肝癌细胞系,可模拟人肝细胞。在 HepaRG 细胞中,N-甲基胞嘧啶显著诱导 CYP3A4 的表达,而这种诱导作用被 PXR 拮抗剂萝卜硫素抑制。这些结果表明,SF 通过激活 PXR 诱导 CYP3A 表达。