Occupancy of glycoprotein IIb/IIIa by B-6 vitamers inhibits human platelet aggregation

J Nutr. 2002 Dec;132(12):3603-6. doi: 10.1093/jn/132.12.3603.

Abstract

Vitamin B-6 inhibits platelet aggregation. However, the effect of the occupancy of GPIIb/IIIa, a major receptor responsible for aggregation on platelet membranes, by B-6 vitamers on platelet aggregation is unknown. This study was carried out to quantify GPIIb/IIIa occupancy in platelets treated with B-6 vitamers [pyridoxal-5-phosphate (PLP); pyridoxal (PL); pyridoxine (PN); pyridoxamine (PM)], using a monoclonal antibody-based assay, by flow cytometry. Antibody binding was compared with inhibition of platelet aggregation. PLP, PL, PN and PM occupied GPIIb/IIIa with dissociation constants of 1.83 +/- 1.15, 19.43 +/- 7.86, 3.63 +/- 1.67 and 10.89 +/- 2.93 mmol/L, respectively. Occupancy of GPIIb/IIIa by the four B-6 vitamers was negatively correlated with platelet aggregation (r = -0.90 to -0.94, P < 0.001). The concentrations of the four B-6 vitamers that inhibited maximal platelet aggregation were in the order of PLP < PN <PM < PL, the same order in which they occupied > or =80% of the GPII/IIIa receptor. Platelet aggregation was inhibited by B-6 vitamers via the occupancy of GPIIb/IIIa with the potency of PLP > PN > PM > PL.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Humans
  • Integrin beta3 / metabolism*
  • Ligands
  • Platelet Aggregation*
  • Platelet Membrane Glycoprotein IIb / metabolism*
  • Protein Binding
  • Vitamin B 6 / metabolism*

Substances

  • Integrin beta3
  • Ligands
  • Platelet Membrane Glycoprotein IIb
  • Vitamin B 6