首页> 外文期刊>Brain research >Expression of endothelial nitric oxide synthase in the ischemic penumbra: relationship to expression of neuronal nitric oxide synthase and vascular endothelial growth factor.
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Expression of endothelial nitric oxide synthase in the ischemic penumbra: relationship to expression of neuronal nitric oxide synthase and vascular endothelial growth factor.

机译:内皮一氧化氮合酶在缺血性半影​​中的表达:与神经元一氧化氮合酶和血管内皮生长因子的表达的关系。

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摘要

Expressional patterns of the endothelial and neuronal forms of nitric oxide synthase (NOS) in cerebral ischemia were studied utilizing a permanent middle cerebral artery occlusion (PMCAO) model. Motor performance and infarct volumes were determined in the rats. Immunohistochemical staining for eNOS, nNOS and neurofilament were performed at 1, 2, 3, 5, 7 and 14 days after PMCAO. Vascular endothelial growth factor (VEGF) expression was determined by in-situ hybridization. PMCAO caused a reproducible cortical infarct with motor deficits in the rats. Double immunohistochemical stainings indicated that eNOS and nNOS were induced in ischemic neurons. Most stained neurons were positive for both NOS forms but some reacted with only one NOS antibody. nNOS expression peaked at 24-48 h after PMCAO, stained mainly the cytoplasm of core neurons, and disappeared after the 3rd day. eNOS expression increased until the 7th day, stained mainly the cytoplasm and membrane of penumbral cells and disappeared by the 14th day after PMCAO. VEGF expression was significantly induced in the penumbral zone in a similar distribution to eNOS. The anatomical and temporal pattern of VEGF and eNOS induction in the brain after permanent ischemia suggest that these mediators may play a role in protecting penumbral tissue from additional ischemic damage.
机译:一氧化氮合酶(NOS)的内皮和神经元形式在脑缺血中的表达模式研究使用永久性大脑中动脉闭塞(PMCAO)模型。确定大鼠的运动表现和梗塞体积。在PMCAO后1、2、3、5、7和14天对eNOS,nNOS和神经丝进行免疫组织化学染色。通过原位杂交确定血管内皮生长因子(VEGF)的表达。 PMCAO在大鼠中引起可再现的皮质梗塞和运动功能障碍。双重免疫组织化学染色表明在缺血性神经元中诱导了eNOS和nNOS。大多数染色的神经元对两种NOS形式均呈阳性,但有些仅与一种NOS抗体反应。 nNOS表达在PMCAO后24-48 h达到高峰,主要染色核心神经元的细胞质,并在第3天后消失。 eNOS表达直到第7天才增加,主要染色半影细胞的细胞质和膜,到PMCAO后第14天消失。在半影区中以与eNOS类似的分布显着诱导VEGF表达。永久性缺血后大脑中VEGF和eNOS诱导的解剖和时间变化模式表明,这些介体可能在保护半影组织免受其他缺血性损伤中发挥作用。

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