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采用凝血酶和纤维蛋白原组成的血栓制作大鼠大脑中动脉栓塞模型。

Embolic middle cerebral artery occlusion model using thrombin and fibrinogen composed clots in rat.

机构信息

Department of Pharmacology & Neuroscience, Institute for Aging and Alzheimer's Disease Research, University of North Texas Health Science Center, Fort Worth, TX 76107, USA.

出版信息

J Neurosci Methods. 2012 Nov 15;211(2):296-304. doi: 10.1016/j.jneumeth.2012.09.006. Epub 2012 Sep 14.

Abstract

Ischemic stroke accounts for over 80% in total human stroke which mostly affect middle cerebral artery (MCA) territory. Embolic stroke models induced by injection of homologous clots into the internal carotid artery and MCA closely mimic human stroke and have been commonly used in stroke research. Studies indicate that the size and composition of clots are critical for the reproducibility of the stroke model. In the present study, we modified the homologous clots formation by addition of thrombin and fibrinogen which produced even distribution of fibrin with tight cross linkage of red blood cells. We optimized the embolic MCA occlusion model in rats using different size of the mixed clots. A precise lodgment of the clots at the MCA bifurcation and highly reproducible ischemic lesion in the MCA territory were demonstrated in the embolic MCA occlusion model induced by injection of 10 pieces of 1-mm long mixed clots made in PE-60 catheter. We further tested the effect of recombinant tissue plasminogen activator (rtPA) in this embolic MCA occlusion model. rtPA induced thrombolysis, improved neurological outcome, and significantly reduced ischemic lesion volume when administered at 1h after embolism as compared with control. In summary, we have established a reproducible embolic MCA occlusion model using clots made of homologous blood, thrombin and fibrinogen. The mixed clots enable precise lodgment at the MCA bifurcation which is responsive to thrombolytic therapy of rtPA.

摘要

缺血性中风占人类中风的 80%以上,主要影响大脑中动脉(MCA)区域。通过将同源血栓注入颈内动脉和 MCA 诱导的栓塞性中风模型非常类似于人类中风,已广泛用于中风研究。研究表明,血栓的大小和成分对于中风模型的可重复性至关重要。在本研究中,我们通过添加凝血酶和纤维蛋白原来修改同源血栓的形成,从而产生纤维蛋白均匀分布,红细胞紧密交联。我们使用不同大小的混合血栓优化了大鼠栓塞 MCA 闭塞模型。在通过向 PE-60 导管中注射 10 个 1mm 长的混合血栓诱导的栓塞 MCA 闭塞模型中,我们证明了血栓在 MCA 分叉处的精确定位和 MCA 区域内高度可重复的缺血性损伤。我们进一步在该栓塞 MCA 闭塞模型中测试了重组组织型纤溶酶原激活剂(rtPA)的效果。与对照组相比,rtPA 在栓塞后 1 小时给药时可诱导血栓溶解,改善神经功能预后,并显著减少缺血性损伤体积。总之,我们使用同源血液、凝血酶和纤维蛋白原制成的血栓建立了一种可重复的栓塞 MCA 闭塞模型。混合血栓可在 MCA 分叉处精确定位,对 rtPA 的溶栓治疗有反应。

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