Thromb Haemost 1992; 68(04): 424-427
DOI: 10.1055/s-0038-1646290
Original Article
Schattauer GmbH Stuttgart

Prevention of Thrombus Growth by Antithrombin III-Dependent and Two Direct Thrombin Inhibitors in Rabbits: Implications for Antithrombotic Therapy

Authors

  • Patrick Brill-Edwards

    1   The Department of Medicine, McMaster University Medical Centre, Hamilton, Ontario, Canada
  • Joanne Van Ryn-McKenna

    2   The Department of Pathology, McMaster University Medical Centre, Hamilton, Ontario, Canada
  • Lu Cai

    2   The Department of Pathology, McMaster University Medical Centre, Hamilton, Ontario, Canada
  • Frederick A Ofosu

    2   The Department of Pathology, McMaster University Medical Centre, Hamilton, Ontario, Canada
    4   The Canadian Red Cross Blood Transfusion Centre, Hamilton, Ontario, Canada
  • Michael R Buchanan

    2   The Department of Pathology, McMaster University Medical Centre, Hamilton, Ontario, Canada
    3   The Department of Surgery, McMaster University Medical Centre, Hamilton, Ontario, Canada
    5   The Department of Hamilton Civic Hospitals Research Centre, Hamilton, Ontario, Canada
Further Information

Publication History

Received 02 January 1992

Accepted after revision 04 May 1992

Publication Date:
04 July 2018 (online)

Preview

Summary

We compared the abilities of heparin and two direct thrombin inhibitors to prevent fibrin accretion onto pre-existing thrombi in rabbits. Inhibition of thrombus growth was measured as the ability of each test compound to inhibit the accretion of 125I-fibrin onto thrombi pre-formed in jugular veins of rabbits. When administered as a continuous infusion, the two direct (i. e. antithrombin III-independent) thrombin inhibitors, r-hirudin and a tripeptide, Ac(D)-Phe-Pro-bor-Arg (P-8714) inhibited fibrin accretion as effectively as heparin, but did so in doses which generated little systemic anticoagulation, as compared to the marked anticoagulation associated with the heparin effect. However, both r-hirudin and P-8714 were more effective when they were administered as a single bolus injection than as a continuous infusion. Under the former conditions, there was only a transient systemic anticoagulant effect. We conclude that direct or antithrombin III-independent thrombin inhibitors are more effective than heparin in preventing thrombus growth. The limited effect of heparin is likely due to fibrin impairing the ability of heparin/antithrombin III to inactivate thrombin.