Thromb Haemost 2006; 96(06): 802-806
DOI: 10.1160/TH06-07-0418
Wound Healing and Inflammation/Infection
Schattauer GmbH

A non-anticoagulant synthetic pentasaccharide reduces inflammation in a murine model of kidney ischemia-reperfusion injury

Authors

  • Rolf Dario Frank

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
    2   Department of Nephrology, University Hospital RWTH Aachen, Aachen, Germany
  • Todd Holscher

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
  • Gernot Schabbauer

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
  • Michael Tencati

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
  • Rafal Pawlinski

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
  • Jeffrey I. Weitz

    3   Departments of Medicine and Biochemistry, McMaster University and Henderson Research Centre, Hamilton, Ontario, Canada
  • Nigel Mackman

    1   Department of Immunology, The Scripps Research Institute, La Jolla, California, USA
Further Information

Publication History

Received 31 July 2006

Accepted after resubmission 12 October 2006

Publication Date:
29 November 2017 (online)

Preview

Summary

Fondaparinux is a synthetic pentasaccharide that selectively inhibits factor Xa (FXa) in an antithrombin-dependent fashion.This newly developed anticoagulant is used in the prevention and treatment of venous thromboembolism. Recently, we showed that fondaparinux reduces inflammation and protects the kidney from ischemia-reperfusion (I/R) injury. However, the relative contributions of the anticoagulant and anti-inflammatory activities of fondaparinux to the observed protection is unknown.To address this, we chemically modified fondaparinux to abolish its affinity for antithrombin and analyzed the effect of this non-anti- coagulant (NAC)-pentasaccharide on binding of U937 cells to P-selectin in vitro and on inflammation in a murine model of kidney I/R injury. NAC-pentasaccharide was as effective as fondaparinux at inhibiting the binding of U937 cells to P-selectin.In addition, NAC-pentasaccharide significantly reduced IL-6 and MIP-2 expression and injury in the kidney I/R model.These findings indicate that the anti-inflammatory activity of fondaparinux can be dissociated from its anticoagulant activity and that NACpentasaccharide is protective in kidney I/R injury.