Key result
Heparin decreased the volume of distribution and clearance of full-length TFPI by a factor of 10-15 in rabbits, whereas the pharmacokinetics of two-domain TFPI were unaffected.
Effect estimate: decreased by a factor 10-15
Heparin may alter full-length TFPI exposure during anticoagulation; leaves open clinical relevance and human translation.
Tissue factor pathway inhibitor (TFPI) is a feed back inhibitor of the initial activation of the extrinsic pathway of coagulation. In humans, injection of heparin results in a 2-6 fold increase in plasma TFPI and recent studies suggest that TFPI may be important for the anticoagulant activity of heparin. Full length (FL) TFPI, but not recombinant two-domain (2D) TFPI, has a poly cationic C-terminus showing very strong heparin binding. Therefore, we have investigated if heparin affects the pharmacokinetics of TFPI with and without this C-terminus. FL-TFPI (608 U/kg) and 2D-TFPI (337 U/kg) were injected intravenously in rabbits with and without simultaneous intravenous injections of low molecular weight heparin (450 anti-XaU/kg). Heparin decreased the volume of distribution and the clearance of FL-TFPI by a factor 10-15, whereas the pharmacokinetics of 2D-TFPI were unaffected by heparin. When heparin was administered 2 h following TFPI the recovery of FL-TFPI was similar to that found in the group receiving the two compounds simultaneously, suggesting that the releasable pool of FL-TFPI is removed very slowly in the absence of circulating heparin.
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Bregengaard et al. (1993) studied this question. Full length (FL) and two-domain (2D) TFPI with low molecular weight heparin vs. TFPI without heparin was evaluated on Pharmacokinetics (volume of distribution and clearance) (decreased by a factor 10-15). Heparin decreased the volume of distribution and clearance of full-length TFPI by a factor of 10-15 in rabbits, whereas the pharmacokinetics of two-domain TFPI were unaffected.
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