Transport and bioactivity of cyanidin 3-glucoside into the vascular endothelium

Free Radic Biol Med. 2012 May 1;52(9):1750-9. doi: 10.1016/j.freeradbiomed.2012.02.027. Epub 2012 Mar 3.

Abstract

Flavonoids are dietary components involved in decreasing oxidative stress in the vascular endothelium and thus the risk of endothelial dysfunction. However, their very low concentrations in plasma place this role in doubt. Thus, a relationship between the effective intracellular concentration of flavonoids and their bioactivity needs to be assessed. This study examined the uptake of physiological concentrations of cyanidin 3-glucoside, a widespread dietary flavonoid, into human vascular endothelial cells. Furthermore, the involvement of the membrane transporter bilitranslocase (TC No. 2.A.65.1.1) as the key underlying molecular mechanism for membrane transport was investigated by using purified anti-sequence antibodies binding at the extracellular domain of the protein. The experimental observations were carried out in isolated plasma membrane vesicles and intact endothelial cells from human endothelial cells (EA.hy926) and on an ischemia-reperfusion model in isolated rat hearts. Cyanidin 3-glucoside was transported via bilitranslocase into endothelial cells, where it acted as a powerful intracellular antioxidant and a cardioprotective agent in the reperfusion phase after ischemia. These findings suggest that dietary flavonoids, despite their limited oral bioavailability and very low postabsorption plasma concentrations, may provide protection against oxidative stress-based cardiovascular diseases. Bilitranslocase, by mediating the cellular uptake of some flavonoids, is thus a key factor in their protective activity on endothelial function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anthocyanins / pharmacokinetics*
  • Biological Transport
  • Cells, Cultured
  • Chromatography, Liquid
  • Endothelium, Vascular / cytology
  • Endothelium, Vascular / metabolism*
  • Glucosides / pharmacokinetics*
  • Humans
  • Mass Spectrometry
  • Rats

Substances

  • Anthocyanins
  • Glucosides
  • cyanidin-3-O-beta-glucopyranoside