Mehrabi Soraya, Janahamdi Mahyar, Joghataie Mohammad Taghi, Barati Mahmood, Marzban Mohsen, Hadjighassem Mahmoudreza, Farahmandfar Maryam
Department of Neuroscience, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Neuroscience Research Center and Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Iran Biomed J. 2018 Jul;22(4):264-74. doi: 10.22034/ibj.22.4.264. Epub 2017 Nov 7.
Many recent epidemiological studies have shown that epileptic patients are more likely suffer from depression, anxiety, and irritability. However, the cellular mechanisms of epilepsy-induced psychotic behaviors are not fully elucidated. Neurotrophin receptors have been suggested to be involved in epilepsy and also in psychiatric disorders. Up-regulation of p75NTR expression and activation of p75NTR signalling cascades after the seizure have been shown, but the role of the p75 receptor in epilepsy-induced psychotic behaviors has not been documented so far. Therefore, the present work aimed to investigate the effect of p75 receptor blockade on seizure activity, irritability, and anxiety-like behaviors in a rat model of status epilepticus.
Rats were injected with pilocarpine (350 mg/ kg, i.p.) to induce status epilepticus. Then various behavioral tests were performed after the blockade of p75NTR alone or in combination with p75 antagonist and phenobarbital. Molecular analysis by PCR was performed to investigate the expression of p75 and pro-NGF.
Molecular findings indicated a high level of mRNA expression for both p75 receptors and pro-NGF in the epileptic model group. Results also showed that the administration of p75 antagonist alone or in combination with phenobarbital was able to significantly influence the behavioral responses. Furthermore, 20-hours video monitoring showed a decrease in the frequency and duration of seizures in the rat group receiving p75 antagonist.
Taken together, the present study suggests that the blockade of the p75 receptor may affect the irritability and anxiety-related behavior in a rat model of status epilepticus.
近期许多流行病学研究表明,癫痫患者更易出现抑郁、焦虑和易怒情绪。然而,癫痫诱发精神行为的细胞机制尚未完全阐明。有研究表明神经营养因子受体与癫痫及精神疾病有关。癫痫发作后p75神经营养因子受体(p75NTR)表达上调及p75NTR信号级联激活已有报道,但p75受体在癫痫诱发精神行为中的作用迄今尚未见文献记载。因此,本研究旨在探讨在癫痫持续状态大鼠模型中阻断p75受体对癫痫发作活动、易怒情绪及焦虑样行为的影响。
给大鼠腹腔注射匹鲁卡品(350mg/kg)诱导癫痫持续状态。然后在单独阻断p75NTR或联合使用p75拮抗剂和苯巴比妥后进行各种行为测试。通过聚合酶链反应(PCR)进行分子分析,以研究p75和前体神经生长因子(pro-NGF)的表达。
分子研究结果表明癫痫模型组中p75受体和pro-NGF的mRNA表达水平较高。结果还显示,单独给予p75拮抗剂或与苯巴比妥联合使用均能显著影响行为反应。此外,20小时的视频监测显示,接受p75拮抗剂的大鼠组癫痫发作的频率和持续时间有所降低。
综上所述,本研究表明阻断p75受体可能会影响癫痫持续状态大鼠模型中的易怒情绪及与焦虑相关的行为。