Protection by Aspirin against Experimentally Induced Arterial Thrombosis in Dogs

C. A Danese; Ch D. Voleti; H. J Weiss

doi:10.1055/s-0038-1654303

Thrombosis and Haemostasis, Table of Contents

Thromb Haemost 1971; 25(02): 288-296
DOI: 10.1055/s-0038-1654303

Originalarbeiten – Original Articles – Travaux Originaux

Schattauer GmbH

Protection by Aspirin against Experimentally Induced Arterial Thrombosis in Dogs

Authors

C. A Danese M. D.

^*Dept. of Surgery, The Mount Sinai School of Medicine, New York, N. Y.
Ch D. Voleti M. D.

^*Dept. of Surgery, The Mount Sinai School of Medicine, New York, N. Y.
H. J Weiss M. D.

^**Division of Hematology (Dept. of Medicine), The Roosevelt Hospital, New York, N. Y.

Abstract

Summary

The possible anti-thrombotic properties of drugs which interfere with platelet aggregation were studied. Segments of the peripheral arteries of dogs were isolated, injured either by endarterectomy or chemically by instillation of 0.1 N H₂ S0₄ (chemical injury). Two days later, the segments were examined for the presence of thrombosis. In animals which received only a placebo, 29% of the chemically-injured segments and 43% of the endarterectomized segments became totally occluded with thrombi. Treatment with aspirin (600 mg per day) reduced this incidence to 2 and 11% respectively (p < .05) while treatment with dipyridamole (DPM) (200 mg per day) had no effect. In a second study, aspirin ingestion reduced the incidence of total occlusion in chemically-injured segments from 38 to 0%. Connective-tissue induced platelet aggregation decreased in aspirin treated animals, while DPM had no effect. The findings support previous suggestions that aspirin, perhaps by inhibiting platelet aggregation, has anti-thrombotic properties.

Full Text

References

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