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作 者:巩守平[1] 王文涛[1] 钟大林[1] 吕健[1] 吴锋[2] 车金[2] 僧志远[1] 贺西京[3]
机构地区:[1]西安交通大学医学院第二附属医院神经外科,陕西西安710004 [2]西安交通大学医学院血液病实验室,陕西西安710004 [3]西安交通大学医学院第二附属医院骨科,陕西西安710004
出 处:《第四军医大学学报》2009年第18期1732-1734,共3页Journal of the Fourth Military Medical University
摘 要:目的:探讨血小板聚集及活化功能在脊髓缺血再灌注损伤(SCIRI)中的变化及谷氨酰胺预处理对其的影响.方法:利用Zivin法建立家兔SCIRI模型,动态监测SCIRI及谷氨酰胺预处理时血小板聚集试验(PAgT)及活化功能特异指标血浆GMP-140浓度的变化.结果:PAgT及GMP-140浓度在缺血45 min逐渐升高,持续至再灌注6 h,与Sham组相比差异显著(P<0.01),于再灌注12 h下降到缺血前水平(P>0.05);谷氨酰胺预处理后血小板进一步活化,高峰期延迟.结论:血小板处于过度活化状态,聚集功能增强,引起凝血功能亢进,可能是参与了脊髓缺血再灌注后神经元损伤与修复过程,谷氨酰胺预处理后血小板进一步活化.AIM: To explore the effect of glutamine precondition on platelet aggregation and activation functions in rats with spinal cord ischemia/reperfusion injury ( SCIRI ). METHODS : SCIRI models were established with Zivin method in rabbits. The platelet aggregation Test(PAgT) and the plasma GMP-140 were observed dynamically. RESULTS: PAgT and GMP-140 concentration in the IR group started to increase at 45 min after ischemia and continued to increased until 6 h after reperfusion, and then decreased to the level before ischemia at 12 h after reperfusion. Glutamine precondition delayed the peak of platelet activation. CONCLUSION: Enhanced PAgT and excessively activated blood platelet function may be involved in the pathological process of SCIRI, which can be activated by glutamine preconditioning.
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