首页> 外文期刊>Neurological Research: An Interdisciplinary Quarterly Journal >Induction of platelet derived-endothelial cell growth factor in the brain after ischemia.
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Induction of platelet derived-endothelial cell growth factor in the brain after ischemia.

机译:缺血后大脑中血小板衍生内皮细胞生长因子的诱导。

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OBJECTIVES: Platelet derived-endothelial cell growth factor (PD-ECGF) is a highly potent angiogenic factor. Although angiogenesis plays an active role in pathophysiology of stroke, the expression pattern of this molecule in ischemic brain has not been investigated. In the present study, therefore, we investigated the change of PD-ECGF expression in the brain after ischemia. METHODS: Using male Wistar rats, the right middle cerebral artery was occluded by a nylon thread for 90 minutes. The animals were decapitated 3 hours, 1, 4 and 10 days after the reperfusion, and frozen sections were prepared. We then performed immunohistochemistry for PD-ECGF and identified the cell phenotype which strongly expressed it by fluorescent double staining. RESULTS: In the sham-operated brain, only small numbers of cells slightly expressed PD-ECGF. The number of positively stained cells increased at the peri-ischemic area from hour 3 of reperfusion. Not only small-sized cells but also large-sized cells became stained. Thenumber of stained cells further increased, and peaked at day 4 for large-sized cells and at day 10 as to small-sized cells. Fluorescent double staining revealed that both large-sized and small-sized cells were neurons, indicating that neurons are the main source of PD-ECGF production in the ischemic brain. DISCUSSION: PD-ECGF has a strong angiogenic property without vascular permeability increasing effect. This molecule may have a therapeutic potential for ischemic stroke treatment.
机译:目的:血小板衍生内皮细胞生长因子(PD-ECGF)是一种高效的血管生成因子。尽管血管生成在中风的病理生理中起积极作用,但尚未研究该分子在缺血性脑中的表达模式。因此,在本研究中,我们研究了缺血后大脑中PD-ECGF表达的变化。方法:使用雄性Wistar大鼠,使用尼龙线将右大脑中动脉闭塞90分钟。在再灌注后3小时,1、4和10天将动物断头,并制备冷冻切片。然后,我们对PD-ECGF进行了免疫组织化学,并通过荧光双染色鉴定了强表达它的细胞表型。结果:在假手术的大脑中,只有少量细胞轻微表达PD-ECGF。从再灌注的第3小时开始,在缺血周围区域阳性染色的细胞数量增加。不仅小细胞而且大细胞都被染色。染色细胞的数量进一步增加,在大型细胞的第4天达到峰值,在小型细胞的第10天达到峰值。荧光双重染色显示大细胞和小细胞都是神经元,表明神经元是缺血性脑中PD-ECGF产生的主要来源。讨论:PD-ECGF具有很强的血管生成特性,而没有增加血管通透性的作用。该分子可能具有缺血性中风治疗的治疗潜力。

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