Thromb Haemost 1985; 54(02): 495-497
DOI: 10.1055/s-0038-1657881
Original Article
Schattauer GmbH Stuttgart

The Effects of Thromboxane Antagonism on the Transit Time of Platelets Through the Spleen

A M Peters
3   Glaxo Group Research Ltd, Ware, UK
,
I F Lane
1   The Department of Surgery, Charing Cross Hospital, London
,
M Sinclair
2   The Department Nuclear Medicine, Charing Cross Hospital, London
,
J T C Irwin
1   The Department of Surgery, Charing Cross Hospital, London
,
C N McCollum
1   The Department of Surgery, Charing Cross Hospital, London
› Institutsangaben
Weitere Informationen

Publikationsverlauf

Received 09. September 1984

Accepted 06. Juni 1985

Publikationsdatum:
18. Juli 2018 (online)

Summary

The spleen is well-known as a site for platelet pooling, although the mechanisms controlling intrasplenic platelet transit are essentially unknown. We tested the possibility that thromboxane A2 might be involved in this control by measuring intrasplenic platelet transit time in 10 subjects receiving a specific thromboxane A2 receptor antagonist (AH23848B; 70 mg; Glaxo Group Research Ltd), in 10 receiving aspirin (300 mg) plus dipyridamole (75 mg), and in 9 receiving placebo. All doses were administered 3 times daily commencing 4 days prior to transit time measurement.

Mean intrasplenic platelet transit time was measured by monitoring the kinetics of equilibration of 111In radiolabelled platelets between blood and spleen following intravenous injection. There was no difference between the mean transit time in the 3 groups of subjects, lending no support to the hypothesis that thromboxane A2 is involved in the control of platelet traffic through the spleen.

 
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