Hanyu S, Ito U, Hakamata Y, Yoshida M
Department of Neurology, Jichi Medical School, Tochigi-ken, Japan.
Acta Neuropathol. 1993;86(1):16-20. doi: 10.1007/BF00454893.
To develop an experimental model which enables quantitative analysis of chronic neuronal loss in the cerebral cortex, repeated ischemic insult was performed using unilateral carotid artery occlusion in Mongolian gerbils. The effect of the time interval between the repeated ischemic insult on the survival rate of the animals and the amount of cortical neuronal loss were examined. The time course of the cortical neuronal damage in repeated ischemic insult was also studied. We repeated the occlusion four times; i.e., one 10-min and three 7-min occlusions (total 31 min of ischemia). The number of animals surviving for 3 weeks after the last ischemic insult was minimum (15.4%) for animals undergoing occlusions at 1-h intervals and maximum (100%) at 24- and 48-h intervals. The number of ischemic neuronal deaths was also dependent upon the time interval, and it was so pronounced as to allow analysis at intervals of 12 hr or 24 hr in the absence of infarction in the cortex. The number of neuronal deaths could not be determined for animals with occlusion at 1-h intervals due to the production of a large infarction, with which the 3-week survival rate was minimum. The temporal profile of cortical neuronal loss in the repeated ischemic insult at 24-h intervals indicated that the number of cortical neurons significantly decreased until 7 days after the start of the ischemic procedure. This model is useful for clarifying the pathophysiology of chronically developing ischemic neuronal death.
为建立一种能够对大脑皮质慢性神经元丢失进行定量分析的实验模型,采用单侧颈动脉闭塞法对蒙古沙鼠进行反复缺血损伤。研究了反复缺血损伤之间的时间间隔对动物存活率和皮质神经元丢失量的影响。还研究了反复缺血损伤中皮质神经元损伤的时间进程。我们重复闭塞四次,即一次10分钟和三次7分钟的闭塞(总共31分钟缺血)。末次缺血损伤后存活3周的动物数量,在间隔1小时进行闭塞的动物中最少(15.4%),在间隔24小时和48小时进行闭塞的动物中最多(100%)。缺血性神经元死亡数量也取决于时间间隔,在皮质无梗死的情况下,间隔12小时或24小时进行分析时这种依赖性非常明显。由于产生大面积梗死,间隔1小时进行闭塞的动物无法确定神经元死亡数量,其3周存活率最低。间隔24小时进行反复缺血损伤时皮质神经元丢失的时间特征表明,直到缺血过程开始后7天,皮质神经元数量显著减少。该模型有助于阐明慢性缺血性神经元死亡的病理生理学。