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缺氧预处理对小鼠局灶性缺血再灌注模型的脑保护作用

Cerebral protection by hypoxic preconditioning in a murine model of focal ischemia-reperfusion.

作者信息

Miller B A, Perez R S, Shah A R, Gonzales E R, Park T S, Gidday J M

机构信息

Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Neuroreport. 2001 Jun 13;12(8):1663-9. doi: 10.1097/00001756-200106130-00030.

Abstract

Sublethal periods of hypoxia or ischemia can induce adaptive mechanisms to protect against subsequent lethal ischemic insults in a process known as ischemic preconditioning. In the present study, we developed a murine model of cerebral preconditioning using several common strains of adult mice. Animals were exposed to sublethal hypoxia (11% oxygen for 2 h) 48 h prior to a 90 min period of transient focal middle cerebral artery occlusion, induced by an intraluminal filament; injury was assessed 24 h later by TTC staining. Infarct volume in hypoxia-preconditioned animals was reduced 46%, 58%, and 64% in C57Bl/6, 129SvEv, and Swiss-Webster ND4 mice relative to their respective untreated controls. This non-invasive murine model of ischemic tolerance should be useful for elucidating the molecular basis of this protection using transgenic and knockout mice.

摘要

亚致死性缺氧或缺血期可诱导适应性机制,以在一个被称为缺血预处理的过程中抵御随后的致死性缺血损伤。在本研究中,我们使用几种成年小鼠的常见品系建立了一种脑预处理的小鼠模型。在通过腔内细丝诱导的90分钟短暂局灶性大脑中动脉闭塞前48小时,将动物暴露于亚致死性缺氧(11%氧气,持续2小时);24小时后通过TTC染色评估损伤情况。与各自未处理的对照组相比,在C57Bl/6、129SvEv和瑞士-韦伯斯特ND4小鼠中,缺氧预处理动物的梗死体积分别减少了46%、58%和64%。这种缺血耐受的非侵入性小鼠模型对于使用转基因和基因敲除小鼠阐明这种保护作用的分子基础应该是有用的。

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