Elucidation the mechanism of the active ingredient imperatorin promoting drug absorption in cell model.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY Journal of Pharmacy and Pharmacology Pub Date : 2024-05-03 DOI:10.1093/jpp/rgad127
Wenjing Ta, Jie Wang, Jihong Song, Xingyue Li, Jianxiang Wang, Wen Lu
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Abstract

Imperatorin (IMP) is the main bioactive furanocoumarin of Angelicae dahuricae radix, which is a well-known traditional Chinese medicine. The purpose of this study was to elucidate the role of IMP in promoting absorption and the possible mechanism on the compatible drugs of Angelicae dahuricae radix. The influence of IMP on drugs' intestinal absorption was conducted by the Caco-2 cell model. The mechanism was studied by investigating the transcellular transport mode of IMP and its influence on P-glycoprotein (P-gp)-mediated efflux, protein expression of P-gp and tight junction, and cell membrane potential. The result showed IMP promoted the uptake of osthole, daidzein, ferulic acid, and puerarin and improved the transport of ferulic acid and puerarin in Caco-2 cells. The absorption-promoting mechanism of IMP might involve the reduction of the cell membrane potential, decrease of P-gp-mediated drug efflux and inhibition of the P-gp expression level in the cellular pathway, and the loosening of the tight junction protein by the downregulation of the expression levels of occludin and claudin-1 in the paracellular pathway. This study provides new insights into the understanding of the improved bioavailability of Angelicae dahuricae radix with its compatible drugs.

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在细胞模型中阐明活性成分御茶精促进药物吸收的机制。
白芷素(IMP)是著名中药白芷的主要生物活性呋喃香豆素。本研究旨在阐明 IMP 促进白芷药物吸收的作用及其可能的机制。通过Caco-2细胞模型研究了IMP对药物肠道吸收的影响。通过研究IMP的跨细胞转运模式及其对P-糖蛋白(P-gp)介导的外排、P-gp和紧密连接蛋白的表达以及细胞膜电位的影响,探讨了IMP对药物肠道吸收的影响机制。结果表明,IMP能促进Caco-2细胞对奥司孔、大豆异黄酮、阿魏酸和葛根素的吸收,并改善阿魏酸和葛根素的转运。IMP 的促进吸收机制可能包括降低细胞膜电位、减少 P-gp 介导的药物外流和抑制细胞通路中 P-gp 的表达水平,以及通过下调细胞旁通路中 occludin 和 claudin-1 的表达水平来松弛紧密连接蛋白。这项研究为了解白芷与其相容性药物的生物利用度的提高提供了新的见解。
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来源期刊
CiteScore
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
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