Thromb Haemost 1984; 51(02): 257-260
DOI: 10.1055/s-0038-1661071
Original Article
Schattauer GmbH Stuttgart

A Comparison of Human Pulmonary Arterial and Venous Prostacyclin and Thromboxane Synthesis- Effect of a Thromboxane Synthase Inhibitor

A J Carter
The Dept. of Medicine, University Hospital, Nottingham, U.K.
,
J A Bevan
The Dept. of Medicine, University Hospital, Nottingham, U.K.
,
S P Hanley
The Dept. of Medicine, University Hospital, Nottingham, U.K.
,
W E Morgan
1   The Dept. of Thoracic Surgery, City Hospital, Nottingham, U. K.
,
D R Turner
2   The Dept. of Histopathology, University Hospital, Nottingham, U. K.
› Author Affiliations
Further Information

Publication History

Received 17 November 1983

Accepted 21 February 1984

Publication Date:
19 July 2018 (online)

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Summary

The amounts of 6-keto-prostaglandin F (6-keto-PGF) and thromboxane B2 (TxB2) produced by the endothelial surfaces of paired samples of human pulmonary arteries and veins, obtained from patients undergoing thoracic surgery, were measured. The amounts of 6-keto-PGF and TxB2 produced by arteries compared with veins were not different. However, both arteries and veins produced more 6-keto-PGF than TxB2, the ratio being approximately 7.5:1 for both. 6-keto-PGF synthesis by arteries was significantly correlated with that produced by veins but the relative amounts of TxB2 were not correlated. 6-keto-PGF synthesis was correlated with TxB2 synthesis for veins but not for arteries. 8 of the 12 arterial samples exhibited some degree of intimal fibrosis.

Incubation with the thromboxane synthase inhibitor, dazoxiben, caused a significant inhibition of vascular TxB2 synthesis and a significant increase in 6-keto-PGF synthesis. In 3 of the 5 cases the increase in 6-keto-PGF was too large to be explained by the fall in TxB2.