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高压氧可减轻局灶性脑缺血中的组织缺氧及缺氧诱导因子-1α表达。

Hyperbaric oxygen reduces tissue hypoxia and hypoxia-inducible factor-1 alpha expression in focal cerebral ischemia.

作者信息

Sun Li, Marti Hugo H, Veltkamp Roland

机构信息

Department of Neurology, Ruprecht-Karls-University Heidelberg, Heidelberg, Germany.

出版信息

Stroke. 2008 Mar;39(3):1000-6. doi: 10.1161/STROKEAHA.107.490599. Epub 2008 Jan 31.

Abstract

BACKGROUND AND PURPOSE

The usefulness of hyperbaric oxygen (HBO) and normobaric hyperoxia in acute ischemic stroke is being reexplored because both improve outcome in experimental cerebral ischemia. However, even the basic mechanisms underlying oxygen therapy are poorly understood. We investigated the effect of both oxygen therapies on tissue hypoxia and on the transcription factor hypoxia-inducible factor-1 alpha.

METHODS

Mice were subjected to filament-induced middle cerebral artery occlusion for 2 hours. Twenty-five minutes after filament introduction, mice breathed normobaric air, normobaric 100% O(2) (normobaric hyperoxia), or 100% O(2) at 3 ata (HBO) for 95 minutes. Hypoxic regions were mapped on tissue sections after preischemic infusion of the in vivo hypoxia marker EF-5. Hypoxia-inducible factor-1 alpha protein was measured after 2-hour middle cerebral artery occlusion using immunofluorescence and immunoblotting. Vascular endothelial growth factor expression was analyzed using in situ mRNA hybridization.

RESULTS

Severity of ischemia did not differ among groups. HBO (35.2+/-10.4 mm(2)) significantly reduced the area of EF-5-stained hypoxic regions in focal cerebral ischemia compared with normobaric hyperoxia (46.4+/-11.2 mm(2)) and air (49.1+/-8 mm(2), P<0.05, analysis of variance). Topographically, EF-5 fluorescence was decreased in medial striatum and in cortical ischemic border areas. Immunohistochemistry and immunoblotting revealed lower hypoxia-inducible factor-1 alpha protein in the ischemic hemisphere of HBO-treated mice. Moreover, mRNA in situ hybridization showed lower expression of vascular endothelial growth factor in HBO and normobaric hyperoxia groups.

CONCLUSIONS

Measurement of extrinsic and intrinsic markers of hypoxia revealed that HBO improves penumbral oxygenation in focal ischemia. Modification of the transcription factor hypoxia-inducible factor-1 alpha and its downstream targets may be involved in effects of HBO.

摘要

背景与目的

由于高压氧(HBO)和常压高氧均能改善实验性脑缺血的预后,因此人们正在重新探讨它们在急性缺血性卒中中的作用。然而,即使是氧疗的基本机制也尚未完全了解。我们研究了这两种氧疗方法对组织缺氧以及转录因子缺氧诱导因子-1α的影响。

方法

小鼠通过丝线诱导大脑中动脉闭塞2小时。在插入丝线25分钟后,小鼠呼吸常压空气、常压100%氧气(常压高氧)或3个绝对大气压下的100%氧气(HBO)95分钟。在缺血前注入体内缺氧标记物EF-5后,在组织切片上绘制缺氧区域图。使用免疫荧光和免疫印迹法在大脑中动脉闭塞2小时后测量缺氧诱导因子-1α蛋白。使用原位mRNA杂交分析血管内皮生长因子的表达。

结果

各组间缺血严重程度无差异。与常压高氧(46.4±11.2平方毫米)和空气组(49.1±8平方毫米,方差分析,P<0.05)相比,HBO(35.2±10.4平方毫米)显著减少了局灶性脑缺血中EF-5染色的缺氧区域面积。在地形学上,内侧纹状体和皮质缺血边界区域的EF-5荧光降低。免疫组织化学和免疫印迹显示,HBO治疗小鼠的缺血半球中缺氧诱导因子-1α蛋白含量较低。此外,原位mRNA杂交显示HBO组和常压高氧组中血管内皮生长因子的表达较低。

结论

对缺氧的外在和内在标志物的测量表明,HBO可改善局灶性缺血半暗带的氧合。转录因子缺氧诱导因子-1α及其下游靶点的改变可能参与了HBO的作用。

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