首页> 外文期刊>Brain research >Hypoxia-ischemia affects erythropoietin and erythropoietin receptor expression pattern in the neonatal rat brain.
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Hypoxia-ischemia affects erythropoietin and erythropoietin receptor expression pattern in the neonatal rat brain.

机译:缺氧缺血影响新生大鼠脑中的促红细胞生成素和促红细胞生成素受体表达模式。

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摘要

Erythropoietin (EPO), known for its role in erythroid differentiation, has been suggested to have non-hematopoietic functions in the brain, especially during development. In the present study, we investigated the expression of erythropoietin and erythropoietin receptor (EPOR) in the developing rat brain following hypoxia-ischemia. Seven-day-old rats underwent unilateral, permanent carotid artery ligation followed by 1 h of hypoxia, and their brains were examined immediately, 24 h or 4 days after hypoxia-ischemia. RT-PCR and Western blot analysis revealed that hypoxia-ischemia only marginally affected EPO expression. Immunohistochemical study of brains 4 days after hypoxia showed that 60 min of hypoxia (resulting in cortical infarction and severe neuronal loss in other regions) led to the increased EPO immunoreactivity, especially in the boundaries of the damaged cerebral cortex, associated with astrocytosis. In contrast, EPOR was dramatically upregulated within 24 h after hypoxia-ischemia. These results suggest that there is a rapid response of EPOR to the hypoxic-ischemic stimulus, which seems to precede that of EPO, leading to the hypothesis that the EPO/EPOR system is implicated in the processes of neuroprotection from hypoxia-ischemia.
机译:促红细胞生成素(EPO)以其在红系分化中的作用而闻名,已被建议在大脑中具有非造血功能,尤其是在发育过程中。在本研究中,我们调查了缺氧缺血后发育中的大鼠脑中促红细胞生成素和促红细胞生成素受体(EPOR)的表达。对7天大的大鼠进行单侧永久性颈动脉结扎,然后缺氧1小时,并在缺氧缺血后24小时或4天立即检查其大脑。 RT-PCR和蛋白质印迹分析表明,缺氧缺血仅轻微影响EPO表达。缺氧4天后对大脑的免疫组织化学研究表明,缺氧60分钟(导致皮质梗塞和其他区域的严重神经元丢失)导致EPO免疫反应性增加,特别是在受损的大脑皮层边界内,与星形细胞增多有关。相反,缺氧缺血后24小时内EPOR显着上调。这些结果表明,EPOR对缺氧缺血性刺激具有快速反应,这似乎早于EPO,导致了这样的假说,即EPO / EPOR系统参与了对缺氧缺血的神经保护过程。

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