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  2. Transport and Interactions of Co-incubated Bi-functional Flavonoids through Inhibiting the Function of P-Glycoprotein (P-gp) Using KB/Multidrug-Resistant (MDR) Cells and Rat Everted Gut Sacs

Transport and Interactions of Co-incubated Bi-functional Flavonoids through Inhibiting the Function of P-Glycoprotein (P-gp) Using KB/Multidrug-Resistant (MDR) Cells and Rat Everted Gut Sacs

  • J Agric Food Chem. 2022 Feb 16;70(6):1923-1933. doi: 10.1021/acs.jafc.1c07694.
Yajing Fang 1 2 Weiwei Cao 3 Mengmeng Xia 1 Siyi Pan 1 Xiaoyun Xu 1
Affiliations

Affiliations

  • 1 Key Laboratory of Environment Correlative Dietology, Ministry of Education, Huazhong Agricultural University, Wuhan 430070, P. R. China.
  • 2 Department of Food Science, Faculty of Science, University of Copenhagen, Frederiksberg C DK-1958, Denmark.
  • 3 College of Food and Bioengineering, Henan University of Science and Technology, Luoyang 471023, P. R. China.
Abstract

This study aims to evaluate the interaction of flavonoid-flavonoid by inhibiting the function of P-glycoprotein (P-gp). The cellular uptake of seven substrates and eleven co-incubated inhibitors was measured in KB/MDR cells. The effect of galangin or morin on the absorption of silibinin or wogonin was carried out in the rat everted gut sacs. Docking was performed to evaluate the interactions between inhibitors and P-gp. Most substrates were greatly enhanced by at least five co-incubated inhibitors. Conversely, the increased uptake of substrates coincided with a decrease or without affecting the uptake of inhibitors, implying a competitive/non-competitive inhibition on P-gp. The enhancement effect by galangin or morin on the transport of silibinin or wogonin was verified in everted gut sacs. Docking explained the inhibition of Flavonoids on P-gp by competitively binding to the ATP site. These results provide a strategy for increasing the absorption of Flavonoids by co-administration.

Keywords

P-glycoprotein; cellular uptake; co-administration; flavonoid inhibitors; flavonoid substrates; molecular docking.

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