The optimal level of vitamin B6, in the form of pyridoxal-5-phosphate (PLP)
, on the antithrombotic effect was investigated in the platelet function an
d blood coagulation of rabbits. Platelet aggregations induced with differen
t agonists, including adenosine diphosphate (ADP, 2.4x10(-4) M), collagen (
0.25 mg/ml), and thrombin (0.3 NIH unit/ml), were assessed in platelet-rich
plasma (PRP) with PLP 0 to 3.0 mM. Thromboxane A2 (TxA2)-production of pla
telet with PLP 0 to 2.4 mM was determined by radiochromatography using C-14
-arachidonic acid as precursor. The blood coagulation system was monitored
by measuring thrombin time (TT), prothrombin time (PT), and partial thrombo
plastin time (PTT) of plasma with PLP 0 to 2.0 mM. PLP significantly inhibi
ted platelet aggregation to different agonists at the final concentration o
f greater than or equal to 0.6 mM and reached the plateau of inhibition at
greater than or equal to 1.8 mM. TxA2-production of PRP was significantly d
ecreased at PLP greater than or equal to 0.36 mM and remained constantly at
greater than or equal to 1.44 mM. PTT, PT, and TT were significantly prolo
nged at PLP greater than or equal to 1.12 mM, greater than or equal to 1.44
mM, and > 1.44 mM, respectively. These results suggested that vitamin B6 d
isplayed antiplatelet and anticoagulation action in rabbits at around 0.36
to 1.8 mM plasma level. (C) 1998 Elsevier Science Inc.