甘草中孕烷X受体激活剂的化学基础☆

Q2 Medicine Liver Research Pub Date : 2022-12-01 DOI:10.1016/j.livres.2022.11.007
Anqi Cheng , Saifei Lei , Junjie Zhu , Jie Lu , Mary F. Paine , Wen Xie , Xiaochao Ma
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引用次数: 2

摘要

背景与目的甘草是甘草属的一种草药补充剂,因其保护肝脏的作用而在世界范围内得到广泛应用。最近的研究引起了人们对肝草通过妊娠X受体(PXR)介导的肝细胞色素P450 3A4 (CYP3A4)的潜在草药相互作用的关注。目前的工作旨在确定甘草中激活PXR和诱导CYP3A4的植物化学物质。方法采用sdpx2细胞进行PXR报告细胞检测。采用代谢组学方法对甘草提取物中的植物化学物质进行了鉴定。在PXR和cyp3a4人源化小鼠模型中进一步研究了从体外研究中鉴定出的PXR激活剂的作用。结果甘草为促pxr活性的中药。甘草中的两种主要植物化学物质甘草酸(glycyrrhizin, GZ)和甘草酸(glycyrrhetinic acid, GA)在基于细胞的报告基因检测中没有激活PXR。然而,光定被证明以剂量依赖的方式激活PXR。体内研究证实GZ不是PXR激活剂,光甘草定是弱PXR激活剂。虽然GA在体外没有激活PXR,但它在PXR和CYP3A4人源化小鼠中以PXR依赖的方式诱导CYP3A4表达。结论sgz不是PXR激活剂。在基于细胞的报告基因试验中,GA不能激活PXR,但在体内可以激活PXR。光定是弱PXR活化剂。本研究通过PXR为肝草相关中草药相互作用的潜在机制提供了新的见解。
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Chemical basis of pregnane X receptor activators in the herbal supplement Gancao (licorice)

Background and aims

The herbal supplement Gancao, also known as licorice, belongs to the genus Glycyrrhiza and has been used worldwide for its hepatoprotective effect. Recent studies have raised concerns about potential herb-drug interactions associated with Gancao via pregnane X receptor (PXR)-mediated induction of hepatic cytochrome P450 3A4 (CYP3A4). The current work aimed to determine the phytochemicals in Gancao that activate PXR and induce CYP3A4.

Methods

DPX2 cells were used for cell-based PXR reporter assays. The phytochemicals in Gancao extract were identified using a metabolomics approach. The effects of PXR activators identified from in vitro studies were further investigated in PXR- and CYP3A4-humanized mouse models.

Results

Gancao was verified to be a PXR-activating herb. Two major phytochemicals in Gancao, glycyrrhizin (GZ) and glycyrrhetinic acid (GA), did not activate PXR in the cell-based reporter assays. However, glabridin was shown to activate PXR in a dose-dependent manner. In vivo studies confirmed that GZ is not a PXR activator and glabridin is a weak PXR activator. Although GA did not active PXR in vitro, it induced CYP3A4 expression in a PXR-dependent manner in the PXR- and CYP3A4-humanized mice.

Conclusions

GZ is not a PXR activator. GA could not activate PXR in cell-based reporter assays but it could activate PXR in vivo. Glabridin is a weak PXR activator. This work provides novel insights into the underlying mechanisms of Gancao-related herb-drug interactions via PXR.

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来源期刊
Liver Research
Liver Research Medicine-Gastroenterology
CiteScore
5.90
自引率
0.00%
发文量
27
审稿时长
13 weeks
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