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首页> 外文期刊>Brain & Development >Erythropoietin exerts neuroprotective effect in neonatal rat model of hypoxic-ischemic brain injury.
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Erythropoietin exerts neuroprotective effect in neonatal rat model of hypoxic-ischemic brain injury.

机译:促红细胞生成素在缺氧缺血性脑损伤的新生大鼠模型中发挥神经保护作用。

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Hypoxic-ischemic encephalopathy seen in survivors of perinatal asphyxia is a frequently encountered and a major clinical problem for which there is currently no effective treatment. Hematopoietic neuroprotective agents, such as erythropoietin (EPO) may rescue neurons from cell death in this setting. EPO is a cytokine hormone that has neuroprotective effect in vitro and in vivo. In this study, we evaluated the effect of posthypoxic EPO administration in an animal model of neonatal hypoxic-ischemic injury. Our results show that a single intracerebroventricular injection of EPO immediately after hypoxic-ischemic insult in neonatal rat model of hypoxic-ischemia reduced the extent of hypoxic-ischemic brain damage. The mean infarct volume assessed 7 days after hypoxia was significantly smaller in EPO-treated group than in the control group. These findings suggest that EPO may provide benefit after hypoxic-ischemic events in the developing brain, a major contributor to static encephalopathy and cerebral palsy.
机译:在围产期窒息幸存者中发现的缺氧缺血性脑病是经常遇到的主要临床问题,目前尚无有效的治疗方法。在这种情况下,造血神经保护剂,例如促红细胞生成素(EPO)可能会使神经元从细胞死亡中解救出来。 EPO是一种细胞因子激素,在体内和体外均具有神经保护作用。在这项研究中,我们评估了在新生儿缺氧缺血性损伤的动物模型中给予低氧后EPO的效果。我们的研究结果表明,在缺氧缺血性新生大鼠模型中,缺氧缺血性损伤后立即单次脑室内注射EPO可降低缺氧缺血性脑损伤的程度。缺氧7天后评估的平均梗塞体积在EPO治疗组中明显小于对照组。这些发现表明,EPO可能在发育中的大脑缺氧缺血事件后提供益处,这是导致静态脑病和脑瘫的主要原因。

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