Thromb Haemost 1981; 46(01): 205
DOI: 10.1055/s-0038-1652598
Platelets – XXI Responses, Calmodulin, Heparin
Schattauer GmbH Stuttgart

On The Mechanism Of Heparin-Induced Potentiation Of Platelet Aggregation

M Yamamoto
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
K Watanabe
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
Y Ando
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
H Iri
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
N Fujiyama
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
K Furihata
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
Y Yoshii
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
K Sugiura
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
Y Ikeda
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
,
K Toyama
Department of Laboratory Medicine and Department of Hematology, Keio University, Tokyo, Japan
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Publikationsverlauf

Publikationsdatum:
24. Juli 2018 (online)

It has been suggested that heparin caused potentiation of aggregation induced by ADP or epinephrine. The exact mechanism of heparin-induced platelet activation, however, remained unknown. In this paper, we have investigated the role of anti-thrombin III ( AT ) in heparin-induced platelet activation using purified AT and AT depleted plasma. When ADP or epinephrine was added to citrated PRP one minute after addition of heparin ( 1 u/ml, porcine intestinal mucosal heparin, Sigma Co. USA ), marked enhancement of platelet aggregation was observed, compared with the degree of aggregation in the absence of heparin. However, in platelet suspensions prepared in modified Tyrode’s solution, heparin exhibited no potentiating effect on platelet aggregation induced by epinephrine or ADP. Potentiation of epinephrine- or ADP-induced platelet aggregation by heparin was demonstrated when purified AT was added to platelet suspensions at a concentration of 20 μg/ml. AT depleted plasma, which was prepared by immunosorption using matrix-bound antibodies to AT, retained no AT, while determination of α1-antitrypsinα2- macroglobulin and fibrinogen in AT depleted plasma produced values which corresponded to those of the original plasma when dilution factor was taken into account. The activities of coagulation factors were also comparable to those of the original plasma. Heparin exhibited potentiating effect on ADP- or epinephrine-induced aggregation of platelets in original plasma, but no effect in AT depleted plasma. When purified AT was added back to AT depleted plasma at a concentration of 20 μg/ml, potentiation of platelet aggregation by heparin was clearly demonstrated.

Our results suggest that effect of heparin on platelet aggregation is also mediated by anti-thrombin III.