孕烷X受体
CYP3A4型
热休克蛋白90
视黄醇X受体
核受体
雄激素受体
免疫印迹
化学
下调和上调
受体
热休克蛋白
生物
细胞生物学
分子生物学
细胞色素P450
生物化学
转录因子
新陈代谢
基因
作者
Lingming Zhang,Jingdi Yan,Jianming Liu,Chao Meng,Fanglan Liu,Chunhua Xia
出处
期刊:Phytomedicine
[Elsevier]
日期:2022-04-06
卷期号:101: 154097-154097
被引量:9
标识
DOI:10.1016/j.phymed.2022.154097
摘要
Cytochrome P450 3A4 (CYP3A4) is one of the most important drug-metabolizing enzymes in the human body, mainly existing in the liver, small intestine, and kidney. Panaxytriol is one of the key active components in red ginseng and Shenmai injection. Our previous study demonstrated that panaxytriol regulates CYP3A4 expression mainly by activating pregnancy X receptor (PXR). At a high concentration of panaxytriol (80 μM), the constitutive androstane receptor (CAR) is also involved in the upregulation of CYP3A4.This study investigated how the cofactors heat shock protein 90 alpha (HSP90α) and retinoid X receptor alpha (RXRα) interact with PXR and CAR to participate in the regulation of CYP3A4 by panaxytriol from the perspective of the PXR and CAR interaction.The mRNA and protein expressions of PXR, CAR, CYP3A4, RXRα, and HSP90α in HepG2 cells and Huh-7 cells were detected by quantitative PCR and western blot analysis, respectively. The binding levels of PXR and CAR to RXRα and HSP90α were determined by co-immunoprecipitation analysis. The nuclear translocation of PXR and RXRα into HepG2 cells and human (hCAR)-silenced HepG2 cells were measured by immunofluorescence.In HepG2 cells and Huh-7 cells, panaxytriol (10-80 μM) upregulated CYP3A4 expression in a concentration-dependent manner by decreasing PXR binding to HSP90α and increasing PXR binding to RXRα. When hCAR was silenced, panaxytriol further enhanced CYP3A4 expression by strengthening PXR binding to RXRα, but it had no significant effect on the binding level of PXR and HSP90α. Additionally, at the high concentration of 80 μM panaxytriol, CAR binding to HSP90α was weakened while binding to RXRα was enhanced.Panaxytriol can upregulate CYP3A4 expression by promoting PXR dissociation from HSP90α and enhancing PXR binding to RXRα in HepG2 cells and Huh-7 cells. At high concentrations of panaxytriol, CAR also participates in the induction of CYP3A4 through a similar mechanism. However, in general, CAR antagonizes PXR binding to RXRα, thereby attenuating the upregulation of CYP3A4 by panaxytriol.
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