» Articles » PMID: 2522336

Inhibitory Effect of a Selective Thromboxane A2 Receptor Antagonist, EP 092, on Platelet Aggregation in Whole Blood Ex Vivo and in Vivo

Overview
Journal Br J Pharmacol
Publisher Wiley
Specialty Pharmacology
Date 1989 Feb 1
PMID 2522336
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

1. The inhibitory effect of a selective prostaglandin H2 (PGH2)/thromboxane A2 receptor antagonist, EP 092, on platelet aggregatory responses in whole blood ex vivo (guinea-pig: Rhesus monkey) and intravascular aggregation in vivo (rabbit) has been investigated. 2. Collagen (0.1-10.0 micrograms ml-1) caused a concentration-dependent decrease in single platelet count in samples of both guinea-pig and Rhesus monkey citrated whole blood incubated ex vivo. EP 092 administered to guinea-pigs by intravenous (0.1-3.0 mg kg-1) or oral (1.0-10.0 mg kg-1) routes significantly inhibited the platelet responses to collagen (ED50 values 1.3 +/- 0.2 and 1.4 +/- 0.2 mg kg-1 respectively). Similar potency against collagen-induced whole blood aggregation was observed in Rhesus monkey blood samples following EP 092 given orally (ED50 0.9 +/- 0.3 mg kg-1). 3. The duration of action of EP 092 against collagen aggregatory responses ex vivo in both guinea-pigs and Rhesus monkeys was between 3 and 6 h following oral administration at 3.0 mg kg-1. 4. The inhibitory activity demonstrated by EP 092 against collagen-induced aggregation of Rhesus monkey whole blood ex vivo was not accompanied by any significant reduction in thromboxane A2 formation except at the highest dose tested (10 mg kg-1). 5. The intravascular aggregatory response induced by collagen or thrombin in the anaesthetized rabbit was significantly inhibited by an intravenous infusion of EP 092 (10 mg kg-1). EP 092 appeared less potent and its effect was of shorter duration in this preparation compared with its inhibitory effect on ex vivo aggregation, being evident immediately after infusion of drug but not after a further 30 min. 6. It is concluded that collagen-induced platelet aggregatory response in guinea-pig and Rhesus monkey whole blood ex vivo and rabbit in vivo exhibit a thromboxane-dependent component which can be inhibited in a dose-related fashion by pretreatment with the thromboxane antagonist EP 092. In the rabbit, moreover, the data support the possibility of a role for thromboxane in the intravascular aggregatory response to thrombin.

Citing Articles

Current concepts for a drug-induced inhibition of formation and action of thromboxane A2.

Patscheke H Blut. 1990; 60(5):261-8.

PMID: 2190651 DOI: 10.1007/BF01736225.

References
1.
Hamberg M, Samuelsson B . Prostaglandin endoperoxides. Novel transformations of arachidonic acid in human platelets. Proc Natl Acad Sci U S A. 1974; 71(9):3400-4. PMC: 433780. DOI: 10.1073/pnas.71.9.3400. View

2.
Marin J, Sanchez-Ferrer C, Salaices M . Effects of ouabain on isolated cerebral and femoral arteries of the cat: a functional and biochemical study. Br J Pharmacol. 1988; 93(1):43-52. PMC: 1853789. DOI: 10.1111/j.1476-5381.1988.tb11403.x. View

3.
Kinlough-Rathbone R, Packham M, Reimers H, Cazenave J, Mustard J . Mechanisms of platelet shape change, aggregation, and release induced by collagen, thrombin, or A23,187. J Lab Clin Med. 1977; 90(4):707-19. View

4.
Addonizio Jr V, EDMUNDS Jr L, Colman R . The function of monkey (M. mulatta) platelets compared to platelets of pig, sheep, and man. J Lab Clin Med. 1978; 91(6):989-97. View

5.
Weksler B, Ley C, Jaffe E . Stimulation of endothelial cell prostacyclin production by thrombin, trypsin, and the ionophore A 23187. J Clin Invest. 1978; 62(5):923-30. PMC: 371849. DOI: 10.1172/JCI109220. View