Haghani Sobhan, Jamali-Raeufy Nida, Zeinivand Motahareh, Mehrabi Soraya, Aryan Leila, Fahanik-Babaei Javad
Department of Physiology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Department of Physiology, School of Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Basic Clin Neurosci. 2021 Nov-Dec;12(6):805-816. doi: 10.32598/bcn.12.5.1944.1. Epub 2021 Nov 1.
Although pharmacotherapy is the most common treatment for epilepsy, proper seizure control is not achieved with current medications. This study evaluated the protective effects of the Hepatocyte Growth Factor (HGF) in a rat model of Temporal Lobe Epilepsy (TLE) and explored possible molecular mechanisms.
A TLE rat model was determined using an intra-hippocampal kainic acid injection (4 μg). Intra-cerebrovascular injection of HGF (6 μg) was performed 30 min before kainic acid injection. Learning and memory impairment were investigated by behavioral tests. The Enzyme-Linked Immunosorbent (ELISA) was used to determine astrogliosis and DNA fragmentation. Changes in neuronal density and mossy fiber sprouting were evaluated by Nissl and Timm staining, respectively.
Behavioral assessments indicated that kainate-treated rats presented spontaneous seizures. Moreover, their alternation percentage scores in the Y-Maze test were lower (P<0.001). Likewise, the passive avoidance test confirmed learning disability in Kainate-treated rats (P<0.001). HGF administration reduced the number of spontaneous seizures, alternation percentage score (P<0.001), and cognitive disturbances (P<0.001). The histopathological results also showed that a protected HGF administration contributed to the reduction of neuronal loss in the CA3 subregion of the hippocampus and inhibited the formation of aberrant Mossy Fiber Sprouting (MFS) (P<0.01). Furthermore, the ELISA data indicated a significant decrease in GFAP (P<0.01) and DNA fragmentation (P<0.05) following HGF administration.
Our findings demonstrated the validity of HGF in protection against the progression of the kainate-induced TLE in rats. This measure improved learning, cognitive disturbances and inhibited apoptosis and astrogliosis.
Temporal lobe epilepsy results in apoptosis of neuronal cells;Hepatocyte growth factor attenuates the severity of status epilepticus in kainic acid-induced model;Hepatocyte growth factor attenuates apoptosis of neuronal cells in kainic acid-induced model of temporal lobe epilepsy.
Epilepsy is known as a disorder of the CNS which is caused by an imbalance in the electrical activity of neurons that in turn results in derangement in cognitive or causing debilitating seizures. Hepatocyte growth factor is one of neurotrophins secreted from mesenchymal and epithelial cells that regulate the growth, survival and functional changes of cells through signaling pathways such as the tyrosine kinase pathway after binding to its specific receptor. In this study, we tried to find out the effect of hepatocyte growth factor on attenuation of the severity of status epilepticus in kainic acid-induced model of temporal lobe epilepsy. Our results show that hepatocyte growth factor is able to protect against progression of the kainate-induced temporal lobe epilepsy in rats by improvement of learning, cognitive disturbances and inhibiting of apoptosis and astrogliosis.
尽管药物治疗是癫痫最常见的治疗方法,但目前的药物并不能实现对癫痫发作的有效控制。本研究评估了肝细胞生长因子(HGF)在颞叶癫痫(TLE)大鼠模型中的保护作用,并探讨了可能的分子机制。
采用海马内注射 kainic 酸(4 μg)建立 TLE 大鼠模型。在注射 kainic 酸前 30 分钟进行脑血管内注射 HGF(6 μg)。通过行为测试研究学习和记忆障碍。采用酶联免疫吸附测定(ELISA)法测定星形胶质细胞增生和 DNA 片段化。分别通过尼氏染色和硫堇染色评估神经元密度变化和苔藓纤维发芽情况。
行为评估表明,用 kainate 处理的大鼠出现自发性癫痫发作。此外,它们在 Y 迷宫试验中的交替百分比得分较低(P<0.001)。同样,被动回避试验证实了用 kainate 处理的大鼠存在学习障碍(P<0.001)。给予 HGF 减少了自发性癫痫发作的次数、交替百分比得分(P<0.001)和认知障碍(P<0.001)。组织病理学结果还显示,给予 HGF 具有保护作用,有助于减少海马 CA3 亚区的神经元损失,并抑制异常苔藓纤维发芽(MFS)的形成(P<0.01)。此外,ELISA 数据表明,给予 HGF 后 GFAP(P<0.01)和 DNA 片段化显著降低(P<0.05)。
我们的研究结果证明了 HGF 在保护大鼠免受 kainate 诱导的 TLE 进展方面的有效性。这一措施改善了学习、认知障碍,并抑制了细胞凋亡和星形胶质细胞增生。
颞叶癫痫导致神经元细胞凋亡;肝细胞生长因子减轻 kainic 酸诱导模型中癫痫持续状态的严重程度;肝细胞生长因子减轻 kainic 酸诱导的颞叶癫痫模型中神经元细胞的凋亡。
癫痫是一种中枢神经系统疾病,由神经元电活动失衡引起,进而导致认知紊乱或使人衰弱的癫痫发作。肝细胞生长因子是间充质和上皮细胞分泌的神经营养因子之一,它通过与特定受体结合后,经酪氨酸激酶途径等信号通路调节细胞的生长、存活和功能变化。在本研究中,我们试图找出肝细胞生长因子对减轻 kainic 酸诱导的颞叶癫痫模型中癫痫持续状态严重程度的影响。我们的结果表明,肝细胞生长因子能够通过改善学习、认知障碍以及抑制细胞凋亡和星形胶质细胞增生,保护大鼠免受 kainate 诱导的颞叶癫痫进展。