Thromb Haemost 1981; 46(02): 538-542
DOI: 10.1055/s-0038-1653405
Original Article
Schattauer GmbH Stuttgart

Testosterone Potentiation of Ionophore and ADP Induced Platelet Aggregation : Relationship to Arachidonic Acid Metabolism

R Pilo
The Department of Biochemistry, The George S. Wise Center of Life Sciences, Tel-Aviv University, Tel-Aviv, Israel
,
D Aharony
The Department of Biochemistry, The George S. Wise Center of Life Sciences, Tel-Aviv University, Tel-Aviv, Israel
,
A Raz
The Department of Biochemistry, The George S. Wise Center of Life Sciences, Tel-Aviv University, Tel-Aviv, Israel
› Author Affiliations
Further Information

Publication History

Received 10 March 1981

Accepted 15 May 1981

Publication Date:
05 July 2018 (online)

Summary

The role of arachidonic acid oxygenated products in human platelet aggregation induced by the ionophore A23187 was investigated. The ionophore produced an increased release of both saturated and unsaturated fatty acids and a concomitant increased formation of TxA2 and other arachidonate products. TxA2 (and possibly other cyclo oxygenase products) appears to have a significant role in ionophore-induced aggregation only when low concentrations (<1 μM) of the ionophore are employed.

Testosterone added to rat or human platelet-rich plasma (PRP) was shown previously to potentiate platelet aggregation induced by ADP, adrenaline, collagen and arachidonic acid (1, 2). We show that testosterone also potentiates ionophore induced aggregation in washed platelets and in PRP. This potentiation was dose and time dependent and resulted from increased lipolysis and concomitant generation of TxA2 and other prostaglandin products. The testosterone potentiating effect was abolished by preincubation of the platelets with indomethacin.

 
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