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首页> 外文期刊>Brain & Development >EPO improved neurologic outcome in rat pups late after traumatic brain injury
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EPO improved neurologic outcome in rat pups late after traumatic brain injury

机译:EPO在创伤性脑损伤后晚期改善大鼠幼鼠的神经系统结果

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In adult rats, erythropoietin improved outcomes early and late after traumatic brain injury, associated with increased levels of Brain Derived Neurotrophic Factor. Using our model of pediatric traumatic brain injury, controlled cortical impact in 17-day old rats, we previously showed that erythropoietin increased hippocampal neuronal fraction in the first two days after injury. Erythropoietin also decreased activation of caspase3, an apoptotic enzyme modulated by Brain Derived Neurotrophic Factor, and improved Novel Object Recognition testing 14 days after injury. Data on long-term effects of erythropoietin on Brain Derived Neurotrophic Factor expression, histology and cognitive function after developmental traumatic brain injury are lacking. We hypothesized that erythropoietin would increase Brain Derived Neurotrophic Factor and improve long-term object recognition in rat pups after controlled cortical impact, associated with increased neuronal fraction in the hippocampus.
机译:在成人大鼠中,创伤性脑损伤早期和晚期促进促红细胞生成素,与脑源性的神经营养因子增加相关。 利用我们的小儿科创伤性脑损伤模型,在17日龄大鼠中控制皮质冲击,我们以前表明促红细胞生成素在损伤后的前两天内增加海马神经元分数。 红细胞生成素还降低了Caspase3的活化,通过脑衍生的神经营养因子调节的凋亡酶,并在损伤后14天改善了新的对象识别测试。 缺乏发育创伤脑损伤后促红细胞生成素对脑源性神经营养因子表达,组织学和认知功能的数据。 我们假设红细胞生成素会增加脑衍生的神经营养因子,并在受控皮质撞击后提高大鼠幼崽的长期对象识别,与海马中的神经元级数增加相关。

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