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Acute Postischemic Seizures Are Associated with Increased Mortality and Brain Damage in Adult Mice

机译:急性缺血性癫痫发作与成年小鼠死亡率增加和脑损伤有关

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摘要

Postischemic seizures are associated with worsened outcome following stroke, but the underlying pathophysiology is poorly understood. Here we examined acute seizures in adult mice following hypoxia–ischemia (HI) via combined behavioral, electrophysiological, and histological assessments. C57BL/6 mice aged 4–9 months received a permanent occlusion of the right common carotid artery and then underwent a systemic hypoxic episode. Generalized motor seizures were observed within 72 h following HI. These seizures occurred nearly exclusively in animals with extensive brain injury in the hemisphere ipsilateral to the carotid occlusion, but their generation was not associated with electroencephalographic discharges in bilateral hippocampal and neocortical recordings. Animals exhibiting these seizures had a high rate of mortality, and post-HI treatments with diazepam and phenytoin greatly suppressed these behavioral seizures and improved post-HI animal survival. Based on these data, we conclude that these seizures are a consequence of HI brain injury, contribute to worsened outcome following HI, and that they originate from deep subcortical structures.
机译:缺血性癫痫发作与中风后转归恶化有关,但对潜在的病理生理了解甚少。在这里,我们通过行为,电生理和组织学综合评估,检查了缺氧缺血(HI)后成年小鼠的急性癫痫发作。 4–9个月大的C57BL / 6小鼠永久性阻塞了右颈总动脉,然后进行了全身性缺氧发作。 HI后72小时内观察到全身运动性癫痫发作。这些癫痫发作几乎仅发生在颈动脉闭塞的同侧半球广泛脑损伤的动物中,但它们的产生与双侧海马和新皮质记录中的脑电图放电无关。表现出这些癫痫发作的动物具有很高的死亡率,用地西epa和苯妥英钠进行的HI后治疗极大地抑制了这些行为性癫痫发作,并改善了HI后动物的存活率。根据这些数据,我们得出结论,这些癫痫发作是HI脑损伤的结果,导致HI后的预后恶化,并且它们源自深层皮质下结构。

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    《Cerebral Cortex》 |2011年第12期|p.2863-2875|共13页
  • 作者

    Liang Zhang;

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