Thromb Haemost 2001; 85(03): 423-429
DOI: 10.1055/s-0037-1615622
Scientific and Standardization Committee Communication
Schattauer GmbH

P-Selectin Antagonism Causes Dose-dependent Venous Thrombosis Inhibition

Autoren

  • Daniel D. Myers

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
  • Robert Schaub

    3   Genetics Institute, Andover, Massachusetts, USA
  • Shirley K. Wrobleski

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
  • Frank J. Londy

    2   Department of Radiology, University of Michigan Medical Center, Ann Arbor, Michigan
  • Beverly A. Fex

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
  • Amy M. Chapman

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
  • Lazar J. Greenfield

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
  • Thomas W. Wakefield

    1   Jobst Vascular Laboratory, Section of Vascular Surgery, Department of Surgery, Unit for Laboratory Animal Medicine
Weitere Informationen

Publikationsverlauf

Received 26. Juli 2000

Accepted after revision 28. September 2000

Publikationsdatum:
08. Dezember 2017 (online)

Summary

Inhibition of P-selectin by antibody or selectin antagonist decreases inflammation and thrombosis. This study evaluates the dose-response relationship using a selectin receptor antagonist. Eight male baboons (Papio anubis) underwent inferior vena caval thrombosis using a 6 h balloon occlusion model. Three animals received 500 μg/kg P-selectin antagonist (rPSGL-Ig) and five 1 mg/kg rPSGL-Ig with or without a non-anticoagulant dose of Dalteparin. These animals were compared to our published results in this model with 4 saline controls and 8 animals that received 4 mg/kg rPSGL-Ig. A statistically significant dose-response relationship existed between rPSGL-Ig dose and thrombosis (p < 0.01), and between rPSGL-Ig dose and spontaneous recanalization (p < 0.05). Inflammatory assessment revealed decreased gadolinium enhancement in all rPSGL-Ig groups compared to previously reported control, despite no significant differences in inflammatory cell extra-vasation. No dose of rPSGL-Ig caused anticoagulation. Selectin antagonism results in a dose-dependent decrease in thrombosis and increase in spontaneous recanalization.