4.7 Article

Natural P-gp inhibitor EGCG improves the acteoside absorption in Caco-2 cell monolayers and increases the oral bioavailability of acteoside in rats

Journal

FOOD AND CHEMICAL TOXICOLOGY
Volume 146, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2020.111827

Keywords

EGCG; Acteoside; P-glycoprotein; Caco-2 monolayers; Bioavailability

Funding

  1. Zhejiang Provincial Major RD Program [2019C02070]
  2. Zhejiang Provincial Basic Public Welfare Research [LGN20C200010]
  3. National Major R&D Program of China [2017YFD0400200, GJFP2019043]
  4. Fundamental Research Funds for the Provincial Universities of Zhejiang Institute of Economics and Trade [19SBYB07]

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Acteoside is one of the most widespread phenylethanoid glycosides with pharmacological activities, including antioxidant, neuroprotective property, etc. However, its bioavailability is poor due to the low absorption and Pgp efflux. This study aimed to select food derived P-gp inhibitors for promoting the acteoside absorption and investigate whether the inhibitors could increase the bioavailability and stability of acteoside. Results showed that EGCG and quercetin significantly decreased the BL-to-AP efflux and promoted the AP-to-BL influx of acteoside across Caco-2 monolayers with optimum concentrations of 320 mu M EGCG or 240 mu M quercetin adding to 320 mu M acteoside. EGCG increased the bioavailability of acteoside to 1.43-fold, but quercetin had no such effect. Further study showed that EGCG and quercetin had no effects on the storage and digestion stability of acteoside. This work revealed that EGCG could improve the acteoside absorption across the Caco-2 monolayers and enhance the bioavailability of acteoside in rats.

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