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Exp Neurol. 2020 Jan;323:113082. doi: 10.1016/j.expneurol.2019.113082. Epub 2019 Oct 24.
2
cGMP-dependent protein kinase I in vascular smooth muscle cells improves ischemic stroke outcome in mice.环鸟苷酸依赖的蛋白激酶 I 在血管平滑肌细胞中改善了小鼠的缺血性脑卒中预后。
J Cereb Blood Flow Metab. 2019 Dec;39(12):2379-2391. doi: 10.1177/0271678X19870583. Epub 2019 Aug 18.
3
Mesenchymal stem cells attenuate blood-brain barrier leakage after cerebral ischemia in mice.间质干细胞减轻小鼠脑缺血后血脑屏障的渗漏。
J Neuroinflammation. 2018 May 3;15(1):135. doi: 10.1186/s12974-018-1153-1.
4
Risk Factors for Poststroke Cognitive Decline: The REGARDS Study (Reasons for Geographic and Racial Differences in Stroke).卒中后认知衰退的危险因素:REGARDS 研究(卒中地理和种族差异的原因)。
Stroke. 2018 Apr;49(4):987-994. doi: 10.1161/STROKEAHA.117.018529. Epub 2018 Mar 16.
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Economic Burden of Informal Caregiving Associated With History of Stroke and Falls Among Older Adults in the U.S.美国老年人中风和跌倒史相关的非正式护理经济负担
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Pharmacological inhibition of myostatin improves skeletal muscle mass and function in a mouse model of stroke.肌肉生长抑制素的药理学抑制可改善卒中模型小鼠的骨骼肌质量和功能。
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7
Animal models of ischaemic stroke and characterisation of the ischaemic penumbra.缺血性中风的动物模型和缺血半影区的特征。
Neuropharmacology. 2018 May 15;134(Pt B):169-177. doi: 10.1016/j.neuropharm.2017.09.022. Epub 2017 Sep 18.
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The IMPROVE Guidelines (Ischaemia Models: Procedural Refinements Of in Vivo Experiments).《IMPROVE指南(缺血模型:体内实验的程序优化)》
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Erythropoietin attenuates axonal injury after middle cerebral artery occlusion in mice.促红细胞生成素可减轻小鼠大脑中动脉闭塞后的轴突损伤。
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10
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改良大脑中动脉闭塞模型提供了详细的术中脑血流登记,并改善了神经行为学评估。

Modified middle cerebral artery occlusion model provides detailed intraoperative cerebral blood flow registration and improves neurobehavioral evaluation.

机构信息

Massachusetts General Hospital, Cardiovascular Research Center, Division of Cardiology, Department of Medicine, Harvard Medical School, Charlestown, MA, USA; Massachusetts General Hospital, Endocrine Unit, Harvard Medical School, Boston, MA, United States(1).

Massachusetts General Hospital, Cardiovascular Research Center, Division of Cardiology, Department of Medicine, Harvard Medical School, Charlestown, MA, USA.

出版信息

J Neurosci Methods. 2021 Jul 1;358:109179. doi: 10.1016/j.jneumeth.2021.109179. Epub 2021 Apr 2.

DOI:10.1016/j.jneumeth.2021.109179
PMID:33819558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8217142/
Abstract

BACKGROUND

Middle cerebral artery occlusion (MCAO) with 1 -h ischemia followed by reperfusion is a widely used stroke model in rodents that has significant limitations such as high mortality and severe neurological deficit hampering comprehensive neurobehavioral evaluation. The goal of this study was to establish a mouse model of 30-minute MCAO followed by 48 h of reperfusion and compare it with 1 -h MCAO followed by 24 h of reperfusion.

NEW METHOD

Here we propose a modified MCAO model that is favorable for both neurobehavioral and infarct volume evaluation. The model includes shorter ischemic time (30 min) of MCAO followed by 48 h of reperfusion and use of standardized intraoperative partial and total reperfusion, which allows for the detailed evaluation of initial and total reperfusion by means of the monitoring of CBF by LDF.

RESULTS AND COMPARISON WITH EXISTING METHOD

Intraoperative CBF parameters and infarct volume (1-h MCAO at 24 h: 69 ± 9; 30-minute MCAO at 48 h: 65 ± 14 mm) did not significantly differ between groups. Neurological deficit was less severe in 30-minute MCAO group where mice also had significantly longer ambulatory distance and time, lower resting time, and higher vertical count on the OPF. The latency to fall in the rotarod test was significantly higher in 30-minute MCAO group. The mortality was higher after 1 -h MCAO.

CONCLUSIONS

30-minute MCAO followed by 48 h of reperfusion causes intraoperative ischemia, reperfusion and infarct volume comparable with 1 -h MCAO followed by 24 h of reperfusion but results in lower mortality with milder neurological deficit allowing for more extensive neurobehavioral evaluation.

摘要

背景

1 小时大脑中动脉闭塞(MCAO)伴缺血再灌注是一种广泛应用于啮齿动物的中风模型,该模型存在较高的死亡率和严重的神经功能缺损,严重限制了全面的神经行为评估。本研究旨在建立一种 30 分钟 MCAO 伴 48 小时再灌注的小鼠模型,并与 1 小时 MCAO 伴 24 小时再灌注模型进行比较。

新方法

我们提出了一种改良的 MCAO 模型,该模型有利于神经行为和梗死体积的评估。模型包括较短的 MCAO 缺血时间(30 分钟),随后是 48 小时的再灌注,以及术中部分和完全再灌注的标准化,这允许通过 LDF 监测 CBF 来详细评估初始和总再灌注。

结果与现有方法的比较

术中 CBF 参数和梗死体积(1 小时 MCAO 24 小时:69±9;30 分钟 MCAO 48 小时:65±14mm)在两组之间没有显著差异。30 分钟 MCAO 组的神经功能缺损较轻,小鼠的步行距离和时间明显较长,休息时间较短,在 OPF 上的垂直计数较高。在转棒试验中,30 分钟 MCAO 组的跌倒潜伏期明显较高。1 小时 MCAO 后死亡率较高。

结论

30 分钟 MCAO 伴 48 小时再灌注引起的术中缺血、再灌注和梗死体积与 1 小时 MCAO 伴 24 小时再灌注相似,但死亡率较低,神经功能缺损较轻,允许更广泛的神经行为评估。