Atlasi Mohammad Ali, Naderian Homayoun, Noureddini Mahdi, Fakharian Esmaeil, Azami Abolfazl
Anatomical Sciences Research Center, Kashan University of Medical Sciences, Kashan, IR Iran.
Physiology Research Center, Kashan University of Medical Sciences, Kashan, IR Iran.
Arch Trauma Res. 2013 Dec;2(3):124-8. doi: 10.5812/atr.10240. Epub 2013 Dec 1.
An appropriate animal model of ischemia stroke is essential for evaluation of different therapeutic methods. Two and four-vessel global ischemia models are one of the most common types of transient cerebral ischemia.
In this study, the morphology of rat hippocampal CA1 neurons in modified models of two and four-vessel ischemia and reperfusion were evaluated.
In this study, 20 Wistar rats were randomly divided into five groups. In group 2 and 3, both common carotid arteries were occluded for 10 minutes in either 3 or 24 hours of reperfusions, respectively. In group 4 and 5, both common carotid and vertebral arteries were occluded for 10 minutes in either 3 or 24 hours of reperfusions, respectively. Group 1 as control, underwent the whole surgery without any arteries occlusion. Hippocampi of the rats in all groups were processed and tissue sections were stained using the Nissl method. The morphology of CA1 neurons were studied under a light microscope and compared different groups.
In all groups ischemic changes were apparently observed in hippocampus CA1 neurons. In two-vessel occlusion model, after 3 and 24 hours of reperfusions, ischemic cells accounted for 14.9% and 23.2%, respectively. In four-vessel occlusion model, after 3 and 24 hours of reperfusions, ischemic cells accounted for 7.6% and 44.9% (P < 0.0001), respectively.
Modified four-vessel occlusion model resulted in significant ischemic changes after 24 hours of reperfusion in CA1 neurons of rat hippocampus.
合适的缺血性中风动物模型对于评估不同治疗方法至关重要。双侧和四动脉全脑缺血模型是最常见的短暂性脑缺血类型之一。
本研究评估了改良的双侧和四动脉缺血再灌注模型中大鼠海马CA1神经元的形态。
本研究中,20只Wistar大鼠随机分为五组。第2组和第3组分别在再灌注3小时或24小时时将双侧颈总动脉闭塞10分钟。第4组和第5组分别在再灌注3小时或24小时时将双侧颈总动脉和椎动脉闭塞10分钟。第1组作为对照组,接受整个手术但不进行任何动脉闭塞。对所有组大鼠的海马进行处理,组织切片采用尼氏染色法染色。在光学显微镜下研究CA1神经元的形态并比较不同组。
所有组海马CA1神经元均明显观察到缺血性改变。在双侧动脉闭塞模型中,再灌注3小时和24小时后,缺血细胞分别占14.9%和23.2%。在四动脉闭塞模型中,再灌注3小时和24小时后,缺血细胞分别占7.6%和44.9%(P<0.0001)。
改良的四动脉闭塞模型在大鼠海马CA1神经元再灌注24小时后导致显著的缺血性改变。