WAY-140312 reduces plasma PAI-1 while maintaining normal platelet aggregation

Biochem Biophys Res Commun. 2003 Nov 28;311(4):904-8. doi: 10.1016/j.bbrc.2003.10.088.

Abstract

Plasminogen activator inhibitor-1 (PAI-1) is the major physiological inhibitor of tissue plasminogen activator (tPA) and is elevated in diseases of vascular remodeling. In this study, we describe an inhibitor of active PAI-1, WAY-140312. Using fluorescence spectroscopy, it was determined that WAY-140312 bound PAI-1 at a single binding site with a dissociation constant of 5 microM. In a biochemical assay determining direct tPA activity, human recombinant PAI-1 completely inhibited tPA, but this inhibition was blocked by WAY-140312 at an IC(50) of 15.6 microM. In vivo, a 10 mg/kg oral dose of WAY-140312 to rats produced a significant plasma reduction of active PAI-1. Bleeding time, thrombin clotting time, and ex vivo platelet aggregation induced by ADP (20 microM) or collagen (2.5 microg/ml) were not affected by administration of WAY-140312. These results are the first to demonstrate that an orally active PAI-1 inhibitor can reduce plasma PAI-1 activity while maintaining normal platelet aggregation and coagulation.

MeSH terms

  • Administration, Oral
  • Animals
  • Blood Coagulation / drug effects*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • Hemorrhage / blood
  • Hemorrhage / metabolism*
  • Humans
  • Male
  • Plasminogen Activator Inhibitor 1 / blood
  • Plasminogen Activator Inhibitor 1 / metabolism*
  • Platelet Aggregation / drug effects*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Plasminogen Activator Inhibitor 1