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[噻氯匹定与血小板功能]

[Ticlopidine and platelet function].

作者信息

Camici M, Evangelisti L

机构信息

Istituto Clinica Medica II, Università degli Studi, Pisa.

出版信息

Minerva Med. 1992 Sep;83(9):525-8.

PMID:1436601
Abstract

In macular degeneration disease of the eye, we have studied the behaviour of vitro thrombocyte aggregation/deaggregation and ex vivo plasma beta-thromboglobulin level (Born aggregometer, RIA kit) during administration of an antiaggregant platelet drug (ticlopidine). We have observed the presence of a prothrombotic state that improves after 15 days of administration of drug. In fact platelet aggregation and beta-thromboglobulin level significantly decrease while thrombocyte deaggregation significantly increase. The correlations between deaggregation, aggregation and beta-thromboglobulin level suggest that the antiaggregant action of the ticlopidine is linked to the inhibition of platelet release reaction.

摘要

在眼部黄斑变性疾病中,我们研究了在使用抗血小板聚集药物(噻氯匹定)期间,体外血小板聚集/解聚行为以及离体血浆β-血小板球蛋白水平(玻恩血小板聚集仪、放射免疫分析试剂盒)。我们观察到存在一种血栓前状态,在给药15天后这种状态有所改善。实际上,血小板聚集和β-血小板球蛋白水平显著降低,而血小板解聚显著增加。解聚、聚集与β-血小板球蛋白水平之间的相关性表明,噻氯匹定的抗聚集作用与抑制血小板释放反应有关。

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