Jp. Herault et al., Effect of factor Xa inhibitors on the platelet-derived microparticles procoagulant activity in vitro and in vivo in rats, THROMB HAEM, 84(4), 2000, pp. 668-674
The aim of this study was to investigate the effect of factor Xa inhibitors
on the prothrombinase activity of platelet-derived microparticles in vitro
and in vivo. The factor Xa inhibitors studied were DX9065A (a direct facto
r Xa inhibitor) and Sanorg34006 (an antithrombin (AT)-mediated factor Xa in
hibitor). Microparticles formed from the platelet surface following activat
ion were isolated by size exclusion gel chromatography. After purification,
their presence was detected by their procoagulant activity and by flow cyt
ometry. Our results show that factor Xa and/or factor Va were present at th
e surface of the platelet-derived microparticles. Prothrombinase formed on
the microparticles was inhibited by factor Xa inhibitors at IC50 values of
0.45 +/- 0.05 and 0.045 +/- 0.005 mu M for DX9065A and AT-Sanore34006 respe
ctively. In an experiment aimed at determining the kinetics: of micropartic
les formation We demonstrated that thrombin tracts were sufficient to induc
t the formation of a significant quantity of microparticles. Both factor Xa
inhibitors delayed the formation of micropanicles by delaying thrombin gen
eration. The thrombogenic effect of the microparticles were studied in vivo
in a modified arterio-venous shunt model in the rat. In this model. the in
crease in the thrombus weigh due to microparticles or phospholipids did not
differ significantly (33% and 23% respectively). In these conditions, prot
hrombinase activity seemed to play a lesser role in the thrombogenic effect
than phospholipids. Nevertheless, factor Xa inhibitors were efficient and
inhibited thrombus formation in a dose-dependent manner.
These results demonstrate that platelet-derived microparticles display a po
tent prothrombotic effect in vivo and show that Factor Xa inhibitors are: p
otent antithrombotic compounds when thrombosis was induced by microparticle
s.