1. Academic Validation
  2. P-glycoprotein (ABCB1) is involved in vitamin K efflux

P-glycoprotein (ABCB1) is involved in vitamin K efflux

  • Food Chem. 2021 May 1;343:128510. doi: 10.1016/j.foodchem.2020.128510.
Marielle Margier 1 Cédric Le May 2 Tiffany Antoine 3 Charlotte Halimi 4 Marion Nowicki 5 Anne Lespine 6 Emmanuelle Reboul 7
Affiliations

Affiliations

  • 1 INRAE, INSERM, Aix Marseille Univ, C2VN, Marseille, France. Electronic address: [email protected].
  • 2 Université de Nantes, CNRS, INSERM, l'institut du thorax, F-44000 Nantes, France. Electronic address: [email protected].
  • 3 INRAE, INSERM, Aix Marseille Univ, C2VN, Marseille, France. Electronic address: [email protected].
  • 4 INRAE, INSERM, Aix Marseille Univ, C2VN, Marseille, France. Electronic address: [email protected].
  • 5 INRAE, INSERM, Aix Marseille Univ, C2VN, Marseille, France. Electronic address: [email protected].
  • 6 INTHERES, Université de Toulouse, INRAE, ENVT, Toulouse, France. Electronic address: [email protected].
  • 7 INRAE, INSERM, Aix Marseille Univ, C2VN, Marseille, France. Electronic address: [email protected].
Abstract

ABCB1 (P-glycoprotein/MDR1) is a multidrug efflux transporter that has previously been involved in Cholesterol and vitamin D metabolism. Our aim was to explore whether ABCB1 is also involved in vitamin K efflux. Vitamin K apical efflux was significantly decreased in presence of ABCB1 inhibitor in Caco-2 cells (-20.4%; p < 0.05) and increased in Griptite cells overexpressing ABCB1 (+40.7%; p < 0.05). In vivo, the vitamin K postprandial response was higher in male Abcb1-/- mice after gavage compared to control Animals (+115%; p < 0.05), but was unchanged in female mice. Finally, a vitamin K transintestinal efflux and a biliary vitamin K efflux were observed, but the specific involvement of ABCB1 could not be confirmed in these pathways. Overall, we showed for the first time that ABCB1 is involved in enterocyte vitamin K efflux in both cell and mouse models and regulates vitamin K absorption in mice.

Keywords

Bile; Bioavailability; Enterocyte; Intestine; MDR1; Phylloquinone.

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