Kim Hyeong-Min, Jo Hyun-Seok, Kim Eun-Jong, Na Ji-Min, Park Hyeng-Kyu, Han Jae-Young, Kim Ki-Hong, Choi Insung, Song Min-Keun
Department of Physical & Rehabilitation Medicine, Chonnam National University Medical School & Hospital, Gwangju 61469, Republic of Korea.
Neurol Int. 2024 Jun 25;16(4):689-700. doi: 10.3390/neurolint16040052.
Diffuse axonal injury (DAI) following sudden acceleration and deceleration can lead to cognitive function decline. Various treatments have been proposed. Repetitive transcranial magnetic stimulation (rTMS), a non-invasive stimulation technique, is a potential treatment for enhancing neuroplasticity in cases of brain injury. The therapeutic efficacy of rTMS on cognitive function remains unconfirmed. This study investigated the effects of rTMS and the underlying molecular biomechanisms using a rat model of DAI. Sprague-Dawley rats (n = 18) were randomly divided into two groups: one receiving rTMS after DAI and the other without brain stimulation. All rats were subjected to sudden acceleration and deceleration using a DAI modeling machine to induce damage. MRI was performed to confirm the DAI lesion. The experimental group received rTMS at a frequency of 1 Hz over the frontal cortex for 10 min daily for five days. To assess spatial memory, we conducted the Morris water maze (MWM) test one day post-brain damage and one day after the five-day intervention. A video tracking system recorded the escape latency. After post-MWM tests, all rats were euthanized, and their brain tissues, particularly from the hippocampus, were collected for immunohistochemistry and western blot analyses. The escape latency showed no difference on the MWM test after DAI, but a significant difference was observed after rTMS between the two groups. Immunohistochemistry and western blot analyses indicated increased expression of BDNF, VEGF, and MAP2 in the hippocampal brain tissue of the DAI-T group. In conclusion, rTMS improved cognitive function in the DAI rat model. The increased expression of BDNF, VEGF, and MAP2 in the DAI-T group supports the potential use of rTMS in treating cognitive impairments associated with DAI.
突然加速和减速后发生的弥漫性轴索损伤(DAI)可导致认知功能下降。人们已经提出了各种治疗方法。重复经颅磁刺激(rTMS)是一种非侵入性刺激技术,是增强脑损伤病例神经可塑性的一种潜在治疗方法。rTMS对认知功能的治疗效果尚未得到证实。本研究使用DAI大鼠模型研究了rTMS的作用及其潜在的分子生物机制。将18只Sprague-Dawley大鼠随机分为两组:一组在DAI后接受rTMS,另一组不进行脑刺激。所有大鼠均使用DAI建模机进行突然加速和减速以诱导损伤。进行MRI以确认DAI损伤。实验组在额叶皮质以1Hz的频率接受rTMS,每天10分钟,共五天。为了评估空间记忆,我们在脑损伤后一天和五天干预后一天进行了莫里斯水迷宫(MWM)测试。视频跟踪系统记录了逃避潜伏期。MWM测试后,所有大鼠均被安乐死,并收集其脑组织,特别是海马组织,用于免疫组织化学和蛋白质印迹分析。DAI后MWM测试的逃避潜伏期无差异,但rTMS后两组之间观察到显著差异。免疫组织化学和蛋白质印迹分析表明,DAI-T组海马脑组织中BDNF、VEGF和MAP2的表达增加。总之,rTMS改善了DAI大鼠模型的认知功能。DAI-T组中BDNF、VEGF和MAP2表达的增加支持了rTMS在治疗与DAI相关的认知障碍中的潜在应用。