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Pharmacodynamic Effects of Sulodexide on Profibrinolytic and Haemorrheological Patterns

Summary

Twenty-four patients with vascular disorders, randomly divided into 3 dosage groups of 8 patients, were treated with a single oral dose of sulodexide (50, 100 or 200mg) and placebo. Tissue plasminogen activator (t-PA), plasminogen activator inhibitor (PAI-1) activity and antigen, euglobulin lysis time, α2-antiplasmin, plasminogen, fibrinogen, blood and plasma viscosity, and whole blood filtration rate were determined before administration and over the following 24 hours. Sulodexide significantly increased t-PA activity linearly with the dose over the range of 50 to 200mg. At the same time, it also significantly decreased the concentration of PAI-1 linearly and proportionally with the dose. No clear effects were observed on the other monitored parameters, although euglobulin lysis time and plasma viscosity showed a tendency to decrease after the administration of sulodexide. These results justify the clinical activity of sulodexide. Indeed, the concomitant increase of t-PA and decrease of PAI-1 activity and antigen might increase the natural fibrinolytic activity with a physiological potentiation, without other adverse effects. The known activity of sulodexide in decreasing plasma viscosity during long term treatment is, however, not immediately explicable by the single-dose effects.

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Messa, G.L., La Placa, G., Puccetti, L. et al. Pharmacodynamic Effects of Sulodexide on Profibrinolytic and Haemorrheological Patterns. Clin. Drug Invest. 10, 165–171 (1995). https://doi.org/10.2165/00044011-199510030-00005

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Keywords

  • Plasminogen Activator
  • Single Oral Dose
  • Plasminogen Activator Inhibitor
  • Drug Invest
  • Pharmacodynamic Effect