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膳食植物化学物作为人类孕烷 X 受体的调节剂。

Dietary phytochemicals as modulators of human pregnane X receptor.

机构信息

College of Food Science and Engineering, Jilin University, Changchun, China.

Department of Pharmacology and Toxicology, Faculty of Pharmacy, Charles University, Hradec Kralove, Czech Republic.

出版信息

Crit Rev Food Sci Nutr. 2023;63(19):3279-3301. doi: 10.1080/10408398.2021.1995322. Epub 2021 Oct 26.

DOI:10.1080/10408398.2021.1995322
PMID:34698593
Abstract

As a promiscuous xenobiotic sensor, pregnane X receptor (PXR) plays a crucial role in drug metabolism. Since dietary phytochemicals exhibit the potential to modulate human PXR, this review aims to summarize the plant-derived PXR modulators, including agonists, partial agonists, and antagonists. The crystal structures of the and ligand-bound forms of PXR especially that of PXR complexed with binary mixtures are summarized, in order to provide the structural basis for PXR binding promiscuity and synergistic activation of PXR by composite ligands. Furthermore, this review summarizes the characterized agonists, partial agonists, and antagonists of human PXR from botanical source. Contrary to PXR agonists, there are only a few antagonists obtained from botanical source due to the promiscuity of PXR. It is worth noting that -resveratrol and a series of methylindoles have been identified as partial agonists of PXR, both in activating PXR function, but also inhibiting the effect of other PXR agonists. Since antagonizing PXR function plays a crucial role in the prevention of drug-drug interactions and improvement of therapeutic efficacy, further research is necessary to screen more plant-derived PXR antagonists in the future. In summary, this review may contribute to understanding the roles of phytochemicals in food-drug and herb-drug interactions.

摘要

作为一种混杂的外源性物质感受器,孕烷 X 受体 (PXR) 在药物代谢中起着至关重要的作用。由于膳食植物化学物质具有调节人 PXR 的潜力,因此本综述旨在总结植物来源的 PXR 调节剂,包括激动剂、部分激动剂和拮抗剂。总结了 PXR 的晶体结构和配体结合形式,特别是 PXR 与二元混合物复合的晶体结构,为 PXR 结合的混杂性和复合配体对 PXR 的协同激活提供了结构基础。此外,本综述还总结了植物来源的人 PXR 的特征性激动剂、部分激动剂和拮抗剂。与 PXR 激动剂不同,由于 PXR 的混杂性,从植物来源获得的拮抗剂很少。值得注意的是,白藜芦醇和一系列甲基吲哚已被鉴定为 PXR 的部分激动剂,既能激活 PXR 功能,又能抑制其他 PXR 激动剂的作用。由于拮抗 PXR 功能在预防药物-药物相互作用和提高治疗效果方面起着至关重要的作用,因此未来有必要进一步研究以筛选更多植物来源的 PXR 拮抗剂。总之,本综述可能有助于理解植物化学物质在食物-药物和草药-药物相互作用中的作用。

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