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Selective white matter abnormalities in a novel rat model of vascular dementia.

机译:新型大鼠血管性痴呆模型中的选择性白质异常。

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摘要

Rats subjected to bilateral common carotid artery (CCA) occlusion or 2-vessel occlusion (2VO) have been used as animal models of subcortical ischemic vascular dementia. However, this model possesses an inherent limitation in that cerebral blood flow (CBF) drops too sharply and substantially after ligation of CCAs. To circumvent such hypoxic-ischemic conditions, we tested implantation of the ameroid constrictor device on bilateral CCAs of male Wistar-Kyoto rats and more precisely replicated chronic cerebral hypoperfusion by gradual narrowing of the CCAs (2-vessel gradual occlusion; 2VGO). The acute cerebral blood flow reduction and resultant inflammatory responses observed in the 2VO rats were eliminated in the 2VGO rats. Thus, chronic cerebral hypoperfusion was segregated, and induced selective white matter changes with relatively preserved neurovascular coupling and substantially less metabolic and histological derangements in the gray matter including the hippocampus. This led to significant spatial working memory impairment of a magnitude similar to the 2VO rats at 28 days postoperation. The 2VGO model may more closely mimic cognitive impairment subsequent to selective white matter damage.
机译:经受双侧颈总动脉(CCA)闭塞或2-血管闭塞(2VO)的大鼠已被用作皮质下缺血性血管性痴呆的动物模型。但是,该模型具有固有的局限性,因为在结扎CCA之后脑血流量(CBF)下降得非常急剧且明显。为了规避这种缺氧缺血性疾病,我们测试了在雄性Wistar-Kyoto大鼠双侧CCA上植入类人猿收缩器的情况,并通过逐渐缩小CCAs(2血管逐渐闭塞; 2VGO)更精确地复制了慢性脑灌注不足。在2VGO大鼠中消除了在2VO大鼠中观察到的急性脑血流量减少和所引起的炎症反应。因此,慢性脑灌注不足被隔离,并诱导了选择性白质的改变,神经血管的耦合相对保留,包括海马体在内的灰质的代谢和组织学紊乱明显减少。这导致明显的空间工作记忆障碍,其程度与术后28天的2VO大鼠相似。 2VGO模型可以更紧密地模拟选择性白质损伤后的认知障碍。

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