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

A M Peters; I F Lane; M Sinclair; J T C Irwin; C N McCollum

doi:10.1055/s-0038-1657881

Thrombosis and Haemostasis, Inhaltsverzeichnis

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

Autor*innen

A M Peters

³Glaxo Group Research Ltd, Ware, UK
I F Lane

¹The Department of Surgery, Charing Cross Hospital, London
M Sinclair

²The Department Nuclear Medicine, Charing Cross Hospital, London
J T C Irwin

¹The Department of Surgery, Charing Cross Hospital, London
C N McCollum

¹The Department of Surgery, Charing Cross Hospital, London

Abstract

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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.

Keywords

Thromboxane - Spleen platelets - ¹¹¹Indium

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Referenzen

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