Department of Neuroscience, Canadian Centre for Behavioural Neuroscience, University of Lethbridge, Lethbridge, AB, Canada.
J Alzheimers Dis. 2018;61(1):283-293. doi: 10.3233/JAD-170635.
In the present study, male C57BL/6J mice were subjected to gradual cerebral hypoperfusion by implanting an ameroid constrictor (AC) on the left common carotid artery (CCA) and a stenosis on the right CCA. In the sham group, all surgical procedures were kept the same except no AC was implanted and stenosis was not performed. One month following the surgical procedures, fear conditioning and object recognition tests were conducted to evaluate learning and memory functions and motor functions were assessed using a balance beam test. At the experimental endpoint, mice were perfused and brains were collected for immunostaining and histology. Learning and memory as well as motor functions were significantly impaired in the hypoperfusion group. The immunoreactivity to choline acetyltransferase was decreased in dorsal striatum and basal forebrain of the hypoperfusion group indicating that cholinergic tone in these brain regions was compromised. In addition, an increased number of Fluoro-Jade positive neurons was also found in cerebral cortex, dorsal striatum and hippocampus indicating neurodegeneration in these brain regions. Based on this pattern of data, we argued that this mouse model would be a useful tool to investigate the therapeutic interventions for the treatment of vascular dementia. Additionally, this model could be employed to exploit the effect of microvascular occlusions on cognitive impairment in the absence and presence of Alzheimer's disease pathology.
在本研究中,雄性 C57BL/6J 小鼠通过在左颈总动脉(CCA)上植入一个缩窄环(AC)和在右 CCA 上形成狭窄来进行逐渐的大脑低灌注。在假手术组中,除了不植入 AC 且不进行狭窄外,所有手术程序均保持相同。在手术程序进行一个月后,进行恐惧条件反射和物体识别测试以评估学习和记忆功能,并使用平衡梁测试评估运动功能。在实验终点时,对小鼠进行灌注并收集大脑进行免疫染色和组织学检查。低灌注组的学习和记忆以及运动功能明显受损。低灌注组背侧纹状体和基底前脑的胆碱乙酰转移酶免疫反应性降低,表明这些脑区的胆碱能张力受损。此外,还发现皮质、背侧纹状体和海马体中氟代-Jade 阳性神经元的数量增加,表明这些脑区的神经退行性变。基于这组数据,我们认为该小鼠模型将是研究血管性痴呆治疗干预措施的有用工具。此外,该模型可用于研究在没有和存在阿尔茨海默病病理的情况下微血管阻塞对认知障碍的影响。