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Post-Traumatic Epilepsy and Seizure Susceptibility in Rat Models of Penetrating and Closed-Head Brain Injury

机译:创伤后癫痫和渗透闭头脑损伤大鼠模型的癫痫发作

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Traumatic brain injury (TBI) carries a risk of developing post-traumatic epilepsy (PTE). Currently, animal models that replicate clinical PTE (delayed spontaneous and recurrent seizures) are limited, which hinders pre-clinical research. In this study, we used two rat models of penetrating ballistic-like brain injury (PBBI) and closed-head injury (CHI) to induce spontaneous seizures and also measure changes in seizure susceptibility. In the PBBI model, two trajectories (frontal and lateral) and two injury severities for each trajectory, were evaluated. In the CHI model, a single projectile impact to the dorsal/lateral region of the head was tested. Continuous video-electroencephalographic (EEG) recordings were collected for 10 days at 1 or 6 month(s) post-injury. After EEG recording, all rats were given a sub-convulsant dose of pentylenetetrazole (PTZ) to challenge the seizure susceptibility. The video-EEG recording did not detect PTE following the PBBI. Only one CHI rat demonstrated persistent and recurrent non-convulsive seizures detected at 6 months post-injury. However, after PTZ challenge, 50-100% of the animals across different TBI groups experienced seizures. Seizure susceptibility increased over time from 1 to 6 months post-injury across the majority of TBI groups. Injury severity effects were not apparent within the PBBI model, but were evident between PBBI and CHI models. These results demonstrated the difficulties in detecting delayed spontaneous post-traumatic seizures even in a high-risk model of penetrating brain injury. The PTZ-induced increase in seizure susceptibility indicated the existence of vulnerable risk of epileptogenesis following TBI, which may be considered as an alternative research tool for pre-clinical studies of PTE.
机译:创伤性脑损伤(TBI)携带开发创伤后癫痫(PTE)的风险。目前,复制临床PTE(延迟自发性和复发癫痫发作)的动物模型是有限的,其妨碍了临床前研究。在这项研究中,我们使用了两种渗透性脑状脑损伤(PBBI)和闭头损伤(CHI)的大鼠模型,以诱发自发癫痫发作,并且还测量癫痫发作易感性的变化。在PBBI模型中,评估了两个轨迹(正面和横向)和两个伤害严重程度,被评估。在CHI模型中,测试了对头部的背/侧区域的单个射弹冲击。损伤后1或6个月收集连续视频脑电图(EEG)录音10天。在EEG记录之后,给所有大鼠都有副惊厥剂剂量的五苯甲酸四唑(PTZ),以攻击癫痫发作敏感性。视频EEG录制未检测到PBBI后的PTE。只有一只奇异大鼠在损伤后6个月检测到持续和复发的非惊厥癫痫发作。然而,在PTZ挑战后,50-100%的不同TBI组的动物经历了癫痫发作。癫痫发作易感性随着时间的推移而增加,大部分TBI群体后损伤后1至6个月增加。在PBBI模型中,伤害严重程度效应并不明显,但在PBBI和CHI模型之间是明显的。这些结果表明,即使在穿透脑损伤的高风险模型中,这些结果表明了检测延迟的自发性后创伤后创伤性癫痫发作。 PTZ诱导的癫痫发作易感性的增加表明TBI后癫痫发生的脆弱风险的存在,这可以被认为是用于PTE的临床前研究的替代研究工具。

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