Thromb Haemost 2003; 90(06): 1054-1060
DOI: 10.1160/TH03-04-0233
Blood Coagulation, Fibrinolysis and Cellular Haemostasis
Schattauer GmbH

Blockade of GPIIb/IIIa by eptifibatide and tirofiban does not alter tissue factor induced thrombin generation in human endotoxemia

Ulla Derhaschnig
1   Departments of Clinical Pharmacology, University of Vienna, Vienna, Austria
2   Emergency Medicine, University of Vienna, Vienna, Austria
,
Christine Pachinger
1   Departments of Clinical Pharmacology, University of Vienna, Vienna, Austria
,
Ingrid Schweeger-Exeli
1   Departments of Clinical Pharmacology, University of Vienna, Vienna, Austria
,
Claudia Marsik
1   Departments of Clinical Pharmacology, University of Vienna, Vienna, Austria
4   Institute for Medical Chemistry and Laboratory Diagnostics, University of Vienna, Vienna, Austria
,
Bernd Jilma
1   Departments of Clinical Pharmacology, University of Vienna, Vienna, Austria
3   Pharmacology, University of Vienna, Vienna, Austria
› Author Affiliations
Further Information

Publication History

Received 17 April 2003

Accepted after resubmission 08 August 2003

Publication Date:
05 December 2017 (online)

Summary

Activated platelets facilitate thrombin generation by providing a catalytic surface on which coagulation activation occurs. The glycoprotein (GP) IIb/IIIa receptor might play a major role in this process as shown by in vitro and animal experiments. However, it is controversial whether the GPIIb/IIIa receptor facilitates tissue factor-induced thrombin generation in humans as well. We therefore investigated whether two clinically used GPIIb/IIIa antagonists (tirofiban and eptifibatide) may blunt TF-induced coagulation in humans.

Thirty male volunteers received 2 ng/kg endotoxin and standard doses of eptifibatide, tirofiban or placebo over 5 hours in a randomized, double-blind, placebo-controlled, double-dummy parallel-group trial. Markers of thrombin generation (prothrom-bin fragment 1+2, thrombin-antithrombin complexes), fibrinoly-sis (D-dimer, plasmin-antiplasmin complexes) as well as inflammatory markers (interleukin-6, tumor necrosis factor-α) were measured by enzyme linked immunoasssays, TF-mRNA expression was quantified by RT-PCR. Neither eptifibatide nor tirofiban influenced LPS-induced coagulation activation or fibrinolytic activity. Additionally, the increase of TNF-α and IL-6 was similar in all groups.

In conclusion, GPIIb/IIIa blockade with eptifibatide or tirofiban did not influence TF-induced coagulation activation in human low grade endotoxemia.

 
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