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首页> 外文期刊>Journal of Neurophysiology >Ischemic injury suppresses hypoxia-induced electrographic seizures and the background EEG in a rat model of perinatal hypoxic-ischemic encephalopathy
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Ischemic injury suppresses hypoxia-induced electrographic seizures and the background EEG in a rat model of perinatal hypoxic-ischemic encephalopathy

机译:缺血性损伤抑制了围产期缺氧缺血性脑病大鼠模型中的缺氧诱导的电图发作和背景脑电图

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The relationship among neonatal seizures, abnormalities of the electroencephalogram (EEG), brain injury, and long-term neurological outcome (e.g., epilepsy) remains controversial. The effects of hypoxia alone (Ha) and hypoxia-ischemia (HI) were studied in neonatal rats at postnatal day 7; both models generate EEG seizures during the 2-h hypoxia treatment, but only HI causes an infarct with severe neuronal degeneration. Single-channel, differential recordings of acute EEG seizures and background suppression were recorded with a novel miniature telemetry device during the hypoxia treatment and analyzed quantitatively. The waveforms of electrographic seizures (and their behavioral correlates) appeared virtually identical in both models and were identified as discrete events with high power in the traditional delta (0.1-4 Hz) and/or alpha (8-12 Hz) bands. Although the EEG patterns during seizures were similar in Ha-and HI-treated animals at the beginning of the hypoxic insult, Ha caused a more severe electrographic seizure profile than HI near the end. Analyses of power spectral density and seizure frequency profiles indicated that the electrographic seizures progressively increased during the 2-h Ha treatment, while HI led to a progressive decrease in the seizures with significant suppression of the EEG background. These data show that 1) the hypoxia component of these two models drives the seizures; 2) the seizures during Ha are substantially more robust than those during HI, possibly because ongoing neuronal damage blunts the electrographic activity; and 3) a progressive decrease in background EEG, rather than the presence of electrographic seizures, indicates neuronal degeneration during perinatal HI.
机译:新生儿癫痫发作,脑电图(EEG)异常,脑损伤和长期神经系统结局(例如癫痫)之间的关系仍然存在争议。在出生后第7天研究了新生大鼠的单独缺氧(Ha)和缺氧缺血(HI)的作用。两种模型在2小时缺氧治疗期间均会产生脑电图发作,但只有HI会导致严重神经元变性的梗塞。在缺氧治疗期间,使用新型微型遥测设备记录急性脑电图发作和背景抑制的单通道差异记录,并进行定量分析。电子癫痫发作的波形(及其行为相关性)在两个模型中看起来几乎相同,并被识别为在传统delta(0.1-4 Hz)和/或alpha(8-12 Hz)波段中具有高功率的离散事件。尽管在缺氧损伤开始时在Ha和HI处理的动物中癫痫发作期间的脑电图模式相似,但Ha引起的电图发作比HI结束时更为严重。功率谱密度和癫痫发作频率图谱的分析表明,在2 h Ha治疗期间,电子照相癫痫发作逐渐增加,而HI导致癫痫发作逐渐减少,而对EEG背景的抑制作用明显。这些数据表明:1)这两种模型的缺氧导致癫痫发作。 2)Ha期间的癫痫发作比HI期间的癫痫发作要强得多,这可能是因为持续的神经元损伤使电描记活动钝化了; 3)背景脑电图的逐渐降低,而不是电子癫痫发作的出现,表明围产期HI期间神经元变性。

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