Effect of a single dose aspirin on platelets in humans with multiple risk factors for coronary artery disease

被引:43
作者
Malinin, AI
Atar, D
Callahan, KP
McKenzie, ME
Serebruany, VL
机构
[1] Johns Hopkins Univ, Sinai Hosp, Thrombosis Res Ctr, Baltimore, MD 21215 USA
[2] Aker Univ Hosp, Div Cardiol, Oslo, Norway
关键词
platelet; aspirin; receptor; coronary artery disease;
D O I
10.1016/S0014-2999(02)02956-4
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We sought to assess how one tablet of non-enteric coated aspirin (325 mg) affects human platelets in subjects with risk factors for coronary artery disease. Data from 63 individuals with multiple cardiac risk factors were analyzed. Platelets were assessed twice at baseline (pre-aspirin), and after 3-4 h (post-aspirin). We employed 5 muM epinephrine-induced conventional aggregometry, closure time with epinephrine/collagen cartridge by PFA-100((R)) (Dade-Behring), and aspirin response units (ARU) stimulated by propyl gallat with Ultegra((R)) (Accumetrics, San Diego, CA, USA) for measuring platelet function. In addition, the expression of platelet receptors was determined by using the following monoclonal antibodies: anti-CD31, CD41, CD42b, CD51/CD61, CD62p, CD63, CD107a, and CD151. Platelet- leukocyte formation was detected utilizing dual antibodies for a pan-platelet marker CD151, and CD14, a monocyte/macrophage marker. PAC-1 was used to measure fibrmogen -platelet binding. One pill of aspirin significantly decreased platelet-rich plasma (PRP) aggregation (74.18+/- 16.75% vs. 24.92+/-8.64%;p<0.0001) and resulted in reduction of the aspirin response units (ARU) (662.24+/- 65.65 vs. 451.05+/-69.31;p<0.0001). There was also prolongation of the closure time (194.4+/-25.3 vs. 258.63+/- 55.61 s;p<0.0001). High correlation (r(2) =0.73-0.86) between platelet analyzer readings and aggregation was observed. One tablet of aspirin moderately inhibited expression of most surface plate let receptors measured, and such inhibition reached significance (p<0.05) for PAC-1, CD31, CD41, CD42, CD62p, and CD151. We conclude that a single dose of aspirin affects major platelet receptors, presumably directly or indirectly through the inhibition of prostanoids via platelet cyclooxygenase-1 blockade. The Ultegra((R)) Analyzer with a novel cartridge seems to be reliable in reflecting aspirins' effects on platelets and could be used in the future in clinical practice for monitoring aspirin therapy. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:139 / 143
页数:5
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