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Recombinant desulphatohirudin (CGP 39393) anticoagulant and antithrombotic properties in vivo.

Abstract
The effects of the newly available biotechnology product, recombinant desulphatohirudin (CGP 39393) have been investigated in rats. This highly potent and selective thrombin inhibitor exhibited marked anticoagulant properties with controllable titration of anticoagulant effect, as measured by activated partial thromboplastin time (APTT), up to nearly four times control values. Furthermore, CGP 39393 exhibited impressive antithrombotic activity in vivo. In an arteriovenous shunt model of thrombus formation on a cotton-thread, the compound was capable of complete inhibition of thrombus development (ED50 = 0.3 mg/kg i.v. and 1.0 mg/kg s.c.). Venous stasis thrombosis was also highly susceptible to inhibition by CGP 39393 (ED50 = 0.01 mg/kg i.v. and 0.45 mg/kg s.c.). Comparison of the anticoagulant and antithrombotic activities of the compound shows that potent antithrombotic effects (83-97% inhibition in the rat shunt model) are achieved within the generally acceptable range of anticoagulation. These results suggest a clear potential for this new agent in the clinical treatment of thrombotic disease.
AuthorsM D Talbot, J Ambler, K D Butler, V S Findlay, K A Mitchell, R F Peters, M F Tweed, R B Wallis
JournalThrombosis and haemostasis (Thromb Haemost) Vol. 61 Issue 1 Pg. 77-80 (Feb 28 1989) ISSN: 0340-6245 [Print] Germany
PMID2749592 (Publication Type: Journal Article)
Chemical References
  • Anticoagulants
  • Antifibrinolytic Agents
  • Hirudins
  • Recombinant Proteins
  • desirudin
Topics
  • Animals
  • Anticoagulants
  • Antifibrinolytic Agents
  • Arteriovenous Shunt, Surgical
  • Hirudins (analogs & derivatives, pharmacology)
  • Ligation
  • Male
  • Partial Thromboplastin Time
  • Rats
  • Rats, Inbred Strains
  • Recombinant Proteins (pharmacology)
  • Thrombosis (etiology, prevention & control)
  • Vena Cava, Inferior

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