Correlation between bleeding time and antithrombotic effect of platelet-suppressive agents in rat experimental model.

A Suehiro, Y Oura, M Ueda, E Kakishita
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Abstract

To examine whether the dosage of a platelet-suppressive agent at which an antithrombotic effect is adequate and bleeding tendency is not increased can be found, the antithrombotic effects, antiplatelet effects and bleeding times of ticlopidine and aspirin were investigated in the rat experimental thrombus formation model. Thrombus formation was determined by measuring the change in wet weight of a silk thread placed in a carotid arteriovenous shunt. Ticlopidine inhibited thrombus formation and platelet aggregation at rather low doses (50-100 mg/kg) without prolonging bleeding time. However, aspirin did not inhibit thrombus formation at even the highest examined dose (200 mg/kg), while bleeding time was prolonged at even the lowest dose (50 mg/kg). These results suggest that a dosage of antithrombotic agent that does not increase bleeding tendency can be easily established using ticlopidine, although it is relatively difficult using aspirin.

大鼠出血时间与血小板抑制剂抗血栓作用的相关性研究。
为了检验一种血小板抑制剂的剂量是否足够且不增加出血倾向,我们在大鼠实验性血栓形成模型中研究噻氯匹定和阿司匹林的抗血栓作用、抗血小板作用和出血次数。通过测量放置在颈动脉动静脉分流管内的丝线湿重的变化来确定血栓的形成。噻氯匹定低剂量(50-100 mg/kg)可抑制血栓形成和血小板聚集,且不延长出血时间。然而,即使在最高剂量(200 mg/kg)下,阿司匹林也不能抑制血栓形成,而即使在最低剂量(50 mg/kg)下,出血时间也会延长。这些结果表明,使用噻氯匹定可以很容易地确定不增加出血倾向的抗血栓药物剂量,尽管使用阿司匹林相对困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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