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阿司匹林与静脉闭塞:对血液纤溶活性和组织型纤溶酶原激活物水平的影响。

Aspirin and venous occlusion: effects on blood fibrinolytic activity and tissue-type plasminogen activator levels.

作者信息

Hammouda M W, Moroz L A

出版信息

Thromb Res. 1986 Apr 1;42(1):73-82. doi: 10.1016/0049-3848(86)90198-2.

Abstract

The effects of oral aspirin (650 mg at 18 and 2 hours before testing) on the response to 10 minute venous occlusion in normal young adults (8 men, 4 women) was examined by fibrinolytic methods (euglobulin lysis, and radiofibrin assay of whole blood and plasma activities) and immunoassay of plasma tissue-type plasminogen activator (tPA). Aspirin had no effect on resting (pre-occlusion) values for any of these. Resting plasma tPA levels were approximately 3-fold greater in men than in women, with or without aspirin. Both before and after aspirin, occlusion increased euglobulin lysis activity, plasma fibrinolytic activity, and plasma tPA levels. In addition, there was an occlusion-related increase in cellular phase activity, determined by radiofibrin assay, which was similar, with and without aspirin, to the increase in plasma activity, indicating the participation of blood cells in the response to occlusion. Mean whole blood activity and cellular phase activity (whole blood less plasma activity) were increased 1.8- and 1.5-fold, respectively, by venous occlusion. In all subjects, the net effect of aspirin on occlusion-related increments in fibrinolytic activity were decreases in whole blood and cellular phase responses (p less than 0.05), without significant effects on plasma or euglobulin lysis activity. In contrast, aspirin treatment resulted in a 32% increase in mean individual increments in plasma tPA concentration with occlusion, an effect predominant in men. Aspirin interferes with the cellular phase fibrinolytic response to venous occlusion, and results in increased, rather than decreased, mean occlusion-induced increments in levels of plasma tissue activator, determined immunochemically.

摘要

通过纤溶方法(优球蛋白溶解以及全血和血浆活性的放射性纤维蛋白测定)和血浆组织型纤溶酶原激活物(tPA)免疫测定,研究了口服阿司匹林(测试前18小时和2小时各服用650毫克)对正常年轻成年人(8名男性,4名女性)10分钟静脉阻塞反应的影响。阿司匹林对这些指标的静息(阻塞前)值均无影响。无论是否服用阿司匹林,男性静息血浆tPA水平均比女性高约3倍。服用阿司匹林前后,阻塞均增加了优球蛋白溶解活性、血浆纤溶活性和血浆tPA水平。此外,通过放射性纤维蛋白测定确定,阻塞相关的细胞期活性增加,无论是否服用阿司匹林,该增加与血浆活性增加相似,表明血细胞参与了对阻塞的反应。静脉阻塞使全血平均活性和细胞期活性(全血活性减去血浆活性)分别增加了1.8倍和1.5倍。在所有受试者中,阿司匹林对阻塞相关纤溶活性增加的净效应是全血和细胞期反应降低(p<0.05),对血浆或优球蛋白溶解活性无显著影响。相比之下,阿司匹林治疗使阻塞时血浆tPA浓度的平均个体增加量提高了32%,这种效应在男性中更为显著。阿司匹林干扰了对静脉阻塞的细胞期纤溶反应,并导致通过免疫化学测定的阻塞诱导的血浆组织激活物水平平均增加,而非降低。

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