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Effects of Natural Polyphenols on the Expression ofDrug Efflux Transporter P-Glycoprotein in Human IntestinalCells

机译:天然多酚对肝癌细胞表达的影响人肠内药物外排转运蛋白P-糖蛋白细胞

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摘要

The drug efflux transporter P-glycoprotein, which is encoded by MDR1 (ABCB1), plays important roles in drug absorption, distribution, and elimination. We previously reported that dietary polyphenols such as quercetin, curcumin, honokiol, magnolol, caffeic acid phenetyl ester (CAPE), xanthohumol, and anacardic acid inhibit P-glycoprotein-mediated drug transport. In the present study, we investigated the effects of polyphenols on the expression of P-glycoprotein using human intestinal epithelial LS174T cells and a reporter plasmid expressing 10.2 kbp of the upstream regulatory region of MDR1. Honokiol, magnolol, CAPE, xanthohumol, and anacardic acid activated the MDR1 promoter in LS174T cells, and the cellular uptake of rhodamine 123 and calcein-AM, fluorescent substrates of P-glycoprotein, decreased in polyphenol-treated LS174T cells. These results suggest that dietary natural polyphenols can induce the drug efflux transporter P-glycoprotein and have the potential to promote food–drug interactions.
机译:由MDR1(ABCB1)编码的药物外排转运蛋白P-糖蛋白在药物吸收,分布和消除中起重要作用。我们之前曾报道过膳食多酚,例如槲皮素,姜黄素,厚朴酚,厚朴酚,咖啡酸苯乙酸酯(CAPE),黄腐酚和抗心酸抑制P-糖蛋白介导的药物转运。在本研究中,我们使用人肠上皮LS174T细胞和表达MDR1上游调节区10.2 kbp的报告质粒,研究了多酚对P-糖蛋白表达的影响。厚朴酚,厚朴酚,CAPE,黄腐酚和漆树酸激活LS174T细胞中的MDR1启动子,而多酚处理的LS174T细胞中若丹明123和钙黄绿素-AM(P-糖蛋白的荧光底物)的细胞摄取减少。这些结果表明,饮食中的天然多酚可以诱导药物外流转运蛋白P-糖蛋白,并具有促进食物与药物相互作用的潜力。

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