| Literature DB >> 8140394 |
K E Karlberg1, J Chen, N Egberg, J Nowak, C Sylvén.
Abstract
In order to assess the ability of three different (one in vivo, one ex vivo and one in vitro) methods to estimate platelet function, 10 healthy volunteers were given a single oral dose of 160 mg ASA. Platelet function was assessed before, 4, 24, 48 and 72 h after dosing by urinary excretion of thromboxane B2, filtragometry and collagen-based whole blood aggregometry. Further, in order to study mechanisms for platelet aggregation in filtragometry, platelet activation was assessed by measurements of beta-thromboglobulin at three different places within the filtragometer test unit in another nine healthy subjects. Four hours after ASA, the aggregation time during filtragometry increased by 213 +/- 133% (p < 0.001) and was parallelled by a decrease in impedance 85 +/- 7% (p < 0.001) indicating an inhibition of platelet aggregability in both tests. A subsequent gradual recovery was observed with both methods. The excretion of thromboxane B2 followed the aggregability pattern being maximally reduced by 72 +/- 6% (p < 0.01) 24 h after ASA and then gradually recovering. All three methods indicated that platelet function was still decreased 72 h after dosing. The urinary excretion of prostacyclin did not change significantly. The results of filtragometry and impedance aggregometry correlated to the logarithm of thromboxane B2 excretion (r = 0.60; p < 0.01 and r = 0.49; p < 0.01, respectively) and to each other (r = 0.70; p < 0.001). In filtragometry beta-thromboglobulin increased significantly (p < 0.05) over the filter.(ABSTRACT TRUNCATED AT 250 WORDS)Entities:
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Year: 1993 PMID: 8140394 DOI: 10.3109/00365519309086496
Source DB: PubMed Journal: Scand J Clin Lab Invest ISSN: 0036-5513 Impact factor: 1.713