Summary
The effects of unfractionated heparin (UH) and recombinant hirudin (rH) on prothrombin
activation, free thrombin generation, and platelet aggregation induced by endogenously
generated thrombin after intrinsic activation of platelet rich plasma were compared.
Free thrombin generation and platelet aggregation were assessed simultaneously by
delaying fibrinogen polymerisation with GPRP.
UH more effectively inhibited prothrombin activation and free thrombin generation
than rH. Increasing concentrations of rH had hardly any effect on the peak amount
of free thrombin, while in the presence of 400 nM UH only traces of free thrombin
were detected. Comparison of TAT and THC (thrombin-hirudin complex) generated until
the onset of platelet aggregation on a molar basis showed that much more thrombin
was inactivated in the presence of rH than in plasma containing UH. The explosive
generation of free thrombin in hirudinized plasmas was accompanied by a markedly steeper
aggregation curve as compared to heparinized plasmas. The generation of thromboxane
B2 was markedly delayed in the presence of UH but not influenced in the presence of
rH.
Our results suggest that UH is more effective than rH in inhibiting prothrombin activation
after intrinsic activation of platelet rich plasma, while rH prevents clotting more
by direct inactivation of already generated thrombin. The inability of even high concentrations
of rH to prevent the explosive generation of free thrombin might contribute to the
observed inefficiency of rH to inhibit platelet aggregation.