Summary
Anticoagulants have been shown to stimulate fibrinolysis principally via inhibition
of thrombin-mediated activation of TAFI (thrombin activatable fibrinolysis inhibitor).
Their profibrinolytic effect,however,may vary according to their mechanism of action
and to the clot composition. We compared the fibrinolytic activity of the direct thrombin
inhibitor melagatran with that of unfractionated heparin in platelet-poor (PPP) and
platelet-rich (PRP) models consisting of tissue-factor-induced clots exposed to exogenous
t-PA (25 ng/ml). In the PPP clot model, both heparin (0.1–0.6 U/ml) and melagatran
(20–320 ng/ml) caused a concentration- dependent shortening of lysis time. However,
when drug profibrinolytic activity (lysis ratio) was expressed in function of the
aPTT prolongation (aPTT ratio), melagatran was more efficient than heparin. In the
PRP clot model, melagatran displayed a fibrinolytic activity fairly comparable to
that observed in PPP whilst heparin caused a modest reduction of lysis time only at
the highest concentrations. Assay of thrombin and TAFIa generation in defibrinated
plasma showed that the presence of platelets markedly reduced the ability of heparin,but
not that of melagatran, to inhibit the formation of these enzymes. Altogether these
data indicate that melagatran is more efficient than heparin in promoting fibrinolysis,
particularly in plateletrich clots, and may thus grant a greater antithrombotic activity
by enhancing thrombus dissolution.
Keywords
Fibrinolysis - anticoagulants - thrombin - TAFI - platelets