Thromb Haemost 1978; 40(02): 542-550
DOI: 10.1055/s-0038-1648687
Original Article
Schattauer GmbH Stuttgart

Inhibition of Platelet Aggregation by a New Agent, Ticlopidine

Shin-Ichiro Ashida
The Laboratory of Biochemistry, Research Institute, Daiichi Seiyaku Co., Ltd. 2810 Minamifunabori-cho, Edogawa-ku, Tokyo 132, Japan
,
Yasushi Abiko
The Laboratory of Biochemistry, Research Institute, Daiichi Seiyaku Co., Ltd. 2810 Minamifunabori-cho, Edogawa-ku, Tokyo 132, Japan
› Author Affiliations
Further Information

Publication History

Received 17 January 1978

Accepted 10 April 1978

Publication Date:
12 July 2018 (online)

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Summary

Effect of Ticlopidine, 5-(2-chlorobenzyl)-4, 5, 6, 7-tetrahydro[3,2-C]pyridine hydrochloride, on platelet aggregation was studied in the rat. Ticlopidine was found to be a potent, long-lasting inhibitor of platelet aggregation. It inhibited the aggregation induced by any of ADP, collagen, thrombin, arachidonic acid and prostaglandin endoperoxides and/or thromboxane A2-like substance. Ticlopidine was effective at doses as low as 30 mg/kg when orally given to rats, and the effect lasted as long as the life span of the circulating platelets (half time: about 48 hours).

Ticlopidine inhibited also nucleotide release from and prostaglandin synthesis in the platelets, but did not significantly affect platelet adhesiveness to glass, platelet factor 3 availability and clot retraction.