Lim Chiyeon, Kim Hongrae, Lim Sehyun, Kim Hyo-Eun, Moon So-Jung, Kim Hyung-Hwan, Cho Suin
Stroke and Neurovascular Regulation Laboratory, Department of Radiology, Massachusetts General Hospital and Harvard Medical School, Charlestown, USA.
Department of Korean Medicine, School of Korean Medicine, Pusan National University, Yangsan, Republic of Korea.
J Cereb Blood Flow Metab. 2025 Jun 26:271678X251352691. doi: 10.1177/0271678X251352691.
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.
小泉和泽亚·隆加的大脑中动脉闭塞(MCAO)模型(KMCAO和LMCAO)是啮齿动物缺血性中风研究中常用的方法。它们之间的一个关键区别在于颈总动脉(CCA)的血流是否得以维持。关于它们病理生理特征的系统比较,尤其是考虑到实验小鼠的年龄,相关证据有限。在本研究中,对3、6、9和12月龄小鼠的脑梗死结果进行了分析。3至6月龄的小鼠采用KMCAO时脑梗死较小,但采用LMCAO时梗死明显,而在9至12月龄的小鼠中差异减小。通过KMCAO诱导缺血1.5小时和LMCAO诱导缺血1小时,在3月龄小鼠中可实现相当的梗死严重程度,这表明可能存在潜在的机制相似性,有待进一步研究。由于保留了CCA灌注,LMCAO导致了再灌注损伤,而KMCAO通过持续结扎CCA提供了可控的缺血性损伤。两种模型均证实,脑损伤增加与神经元核表达降低和胶质纤维酸性蛋白表达增加相关。这些发现凸显了根据实验目的、年龄和缺血持续时间选择MCAO模型对于准确模拟缺血性和退行性脑损伤的重要性。