评估衰老对小泉和Zea Longa方法的影响及其作为评估缺血性中风后神经变性的小鼠模型的适用性:一项比较研究。

Chiyeon Lim, Hongrae Kim, Sehyun Lim, Hyo-Eun Kim, So-Jung Moon, Hyung-Hwan Kim, Suin Cho
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引用次数: 0

摘要

小泉(Koizumi)和泽龙贺(Zea Longa)的大脑中动脉闭塞(MCAO)模型(KMCAO和LMCAO)是啮齿动物缺血性脑卒中研究中常用的方法。它们之间的一个关键区别在于是否维持颈总动脉(CCA)的血液流动。关于它们的病理生理特征的系统比较,特别是考虑到实验小鼠的年龄,证据有限。在这项研究中,分析了3、6、9和12个月大的小鼠脑梗死的结果。3-6月龄小鼠KMCAO表现为轻度脑梗死,而LMCAO表现为重度脑梗死,而9-12月龄小鼠的差异减弱。用KMCAO诱导缺血1.5小时和用LMCAO诱导缺血1小时,3月龄小鼠的梗死严重程度相当,提示潜在的机制相似性,有待进一步研究。LMCAO通过保留CCA灌注导致再灌注损伤,而KMCAO通过持续结扎CCA提供可控的缺血损伤。两种模型均证实脑损伤增加与神经元核表达减少和胶质原纤维酸性蛋白表达增加相关。这些发现强调了根据实验目的、年龄和缺血持续时间选择MCAO模型对于准确建模缺血性和退行性脑损伤的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the effects of aging on the Koizumi's and Zea Longa's methods and their suitability as mouse models for evaluating neurodegeneration post-ischemic stroke: A comparative study.

Koizumi's and Zea Longa's middle cerebral artery occlusion (MCAO) models (KMCAO and LMCAO) are commonly used methods in rodent ischemic stroke research. A key distinction between them lies in whether the blood flow through the common carotid artery (CCA) is maintained. Limited evidence exists regarding the systematic comparison of their pathophysiological characteristics, particularly considering the age of experimental mice. In this study, cerebral infarction outcomes were analyzed in mice aged 3, 6, 9, and 12 months. Mice aged 3-6 months exhibited minor cerebral infarction with KMCAO but substantial infarction with LMCAO, whereas differences diminished in 9-12-month-old mice. Comparable infarct severity in 3-month-old mice was achieved by inducing ischemia for 1.5 hours using KMCAO and for 1 hour using LMCAO, suggesting potential mechanistic similarities, subject to further research. LMCAO led to reperfusion injury due to preserved CCA perfusion, whereas KMCAO provided controlled ischemic insult via continuous CCA ligation. Both models confirmed that increased brain damage correlated with decreased neuronal nuclei expression and increased glial fibrillary acidic protein expression. These findings highlight the importance of selecting the MCAO model based on experimental objectives, age, and ischemia duration for the accurate modeling of ischemic and degenerative brain injury.

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