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Low-dose aspirin inhibits platelet-induced contraction of the human isolated coronary artery. A role for additional 5-hydroxytryptamine receptor antagonism against coronary vasospasm?
Author(s) -
Willem A. Bax,
G.J. Renzenbrink,
E A van der Linden,
Felix Zijlstra,
D. van Heuven-Nolsen,
Durk Fekkes,
Egbert Bos,
P.R. Saxena
Publication year - 1994
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/01.cir.89.2.623
Subject(s) - medicine , platelet , aspirin , contraction (grammar) , ketanserin , thromboxane a2 , thromboxane , antagonist , receptor antagonist , artery , vasospasm , endocrinology , platelet activation , platelet aggregation inhibitor , pharmacology , receptor , serotonin , 5 ht receptor , subarachnoid hemorrhage
The beneficial effect of low-dose aspirin in the prevention of coronary vasospasm is well documented. In this study, we investigated the contractile effect of human washed platelets on the human isolated coronary artery. We concentrated on the effect of low-dose aspirin (40 mg/d) taken by the platelet donor and on the efficacy of thromboxane A2 (TXA2) and 5-hydroxytryptamine (5-HT) receptor antagonists.

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