Department of Pediatrics, Division of Neurology, School of Medicine, Translational Epilepsy Research Program, University of Colorado Anschutz Medical Campus, Aurora, Colorado, U.S.A.
Epilepsia. 2014 Jul;55(7):985-93. doi: 10.1111/epi.12646. Epub 2014 May 16.
In this study, we use time-locked video and electroencephalography (EEG) recordings to characterize acute seizures and EEG abnormalities in an animal model that replicates many salient features of human neonatal hypoxic-ischemic encephalopathy (HIE) including the brain injury pattern and long-term neurologic outcome.
Hypoxia-ischemia (HI) was induced in 7-day-old rats by ligating the right carotid artery and exposing the pups to hypoxia for 2 h (Rice-Vannucci method). To identify seizures and abnormal EEG activity, pups were monitored by video-EEG during hypoxia and at various time points after HI. Occurrence of electroclinical seizures, purely electrographic seizures and other abnormal discharges on EEG, was quantified manually. A power spectrum analysis was done to evaluate the effects of HI on EEG spectra in the 1-50 Hz frequency band.
During hypoxia, all pups exhibit short duration, but frequent electroclinical seizures. Almost all pups continue to have seizures in the immediate period following termination of hypoxia. In more than half of the HI rats, seizures persisted for 24 h; for some of them, the seizures continued for >48 h. Seizures were not observed in any rats at 72 h after HI induction. A significant reduction in background EEG voltage in the cortex ipsilateral to the ligated carotid artery occurred in rats subjected to HI. In addition, purely electrographic seizures, spikes, sharp waves, and brief runs of epileptiform discharges (BREDs) were also observed in these rats.
HI induction in P7 rats using the Rice-Vannucci method resulted in the development of seizures and EEG abnormalities similar to that seen in human neonates with HIE. Therefore, we conclude that this is a valid model to test the efficacy of novel interventions to treat neonatal seizures.
本研究通过时相关视频和脑电图(EEG)记录,来描述一种动物模型中的急性发作和 EEG 异常,该模型复制了许多人类新生儿缺氧缺血性脑病(HIE)的显著特征,包括脑损伤模式和长期神经学结局。
通过结扎 7 日龄大鼠右侧颈总动脉并将幼仔暴露于缺氧 2 小时(Rice-Vannucci 法)来诱导缺氧缺血(HI)。为了识别发作和异常 EEG 活动,通过视频-EEG 在缺氧期间以及 HI 后各个时间点监测幼仔。手动量化电临床发作、纯脑电图发作和 EEG 上的其他异常放电的发生。进行功率谱分析以评估 HI 对 1-50 Hz 频带内 EEG 频谱的影响。
在缺氧期间,所有幼仔均表现出短暂但频繁的电临床发作。几乎所有幼仔在缺氧结束后立即仍持续发作。在超过一半的 HI 大鼠中,发作持续 24 小时;其中一些大鼠的发作持续超过 48 小时。HI 诱导后 72 小时,在任何大鼠中均未观察到发作。接受 HI 的大鼠结扎侧大脑皮层的背景 EEG 电压显著降低。此外,还观察到这些大鼠中存在纯脑电图发作、棘波、尖波和短暂的癫痫样放电发作(BRED)。
使用 Rice-Vannucci 法在 P7 大鼠中诱导 HI 导致了类似于人类 HIE 新生儿所见的发作和 EEG 异常的发展。因此,我们得出结论,这是一种有效的模型,可以测试治疗新生儿发作的新干预措施的疗效。