Thromb Haemost 1981; 46(03): 590-592
DOI: 10.1055/s-0038-1653424
Original Article
Schattauer GmbH Stuttgart

The In Vitro Effect of Ticlopidine on Fibrinogen and Factor VIII Binding to Human Platelets

Helen Lee
The Laboratoire d’Hémostase et de Thrombose Expérimentale, Hôpital Saint-Louis, Paris, France
,
R C Paton
*   The Service de Nutrition et Endocrinologie, Hôpital Saint-Louis, Paris, France
,
C Ruan
The Laboratoire d’Hémostase et de Thrombose Expérimentale, Hôpital Saint-Louis, Paris, France
,
J P Caen
The Laboratoire d’Hémostase et de Thrombose Expérimentale, Hôpital Saint-Louis, Paris, France
› Author Affiliations
Further Information

Publication History

Received 02 March 1981

Accepted 19 June 1981

Publication Date:
05 July 2018 (online)

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Summary

The mode of action of the antiplatelet agent ticlopidine is not yet fully understood. Its multiple effects on platelet function include prolongation of the bleeding time, reduction in primary and secondary Waves of ADP-induced aggregation and inhibition of collagen and thrombin-induced aggregation. We have studied the in vitro effects of ticlopidine on fibrinogen binding induced by ADP and adrenaline as well as factor VIII/vWF binding induced by ristocetin.

125I-fibrinogen binding was measured in suspensions of freshly washed normal platelets stimulated by 10 μM ADP or 10 μM adrenaline. The binding of 125I-factor VIII/vWF in the presence of 1 mg/ml ristocetin was measured in both washed and paraformaldehyde-fixed platelets. Ticlopidine at final concentrations of 200, 100, 50 and 25 μM inhibited both ADP and adrenaline-induced fibrinogen binding in a dose-dependent manner. The mean % inhibition of ADP-induced fibrinogen binding was 82, 73, 42 and 32 respectively. The mean % inhibition of adrenaline induced fibrinogen binding was 86, 82, 60 and 35 respectively. In contrast, the factor VIII/vWF binding was unaffected by ticlopidine at all concentrations except at 200 μM using fresh platelets where a slight inhibition (19%) was observed.

These results suggest that ticlopidine either inhibits platelet activation and consequently fibrinogen binding, or inhibits the binding directly, presumably by having an effect on the specific configuration of the platelet membrane required for normal fibrinogen binding.