Department of Physiology and Pharmacology, West Virginia University, Morgantown, WV, 26506, USA.
Department of Neuroscience, West Virginia University, Morgantown, WV, 26506, USA.
Metab Brain Dis. 2018 Dec;33(6):2039-2044. doi: 10.1007/s11011-018-0312-5. Epub 2018 Sep 28.
Chronic cerebrovascular hypoperfusion results in vascular dementia and increases predisposition to lacunar infarcts. However, there are no suitable animal models. In this study, we developed a novel model for chronic irreversible cerebral hypoperfusion in mice. Briefly, an ameroid constrictor was placed on the right carotid artery to gradually occlude the vessel, while a microcoil was placed on the left carotid artery to prevent compensation of the blood flow. This procedure resulted in a gradual hypoperfusion developing over a period of 34 days with no cerebral blood flow recovery. Histological analysis of the brain revealed neuronal and axonal degeneration as well as necrotic lesions. The most severely affected regions were located in the hippocampus and the corpus callosum. Overall, our paradigm is a viable model to study brain pathology resulting from gradual cerebrovascular hypoperfusion.
慢性脑血管灌注不足可导致血管性痴呆,并增加腔隙性梗死的易感性。然而,目前尚无合适的动物模型。在本研究中,我们在小鼠中建立了一种新的慢性不可逆性脑灌注不足模型。简而言之,在右侧颈总动脉上放置一个缩窄环以逐渐阻塞血管,同时在左侧颈总动脉上放置一个微线圈以防止血流代偿。这一过程导致在 34 天的时间内逐渐出现低灌注,且无脑血流恢复。对大脑进行组织学分析显示神经元和轴突变性以及坏死病变。受影响最严重的区域位于海马体和胼胝体。总的来说,我们的实验方案是研究由于慢性脑血管灌注不足引起的脑病理学的可行模型。