Lu Xia, Bao Xinjie, Li Jiantao, Zhang Guanghao, Guan Jian, Gao Yunzhou, Wu Peilin, Zhu Zhaohui, Huo Xiaolin, Wang Renzhi
Department of Neurosurgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100005, P.R. China.
Laboratory of Bioelectromagnetics, Institute of Electrical Engineering, Chinese Academy of Sciences, Beijing 100190, P.R. China.
Exp Ther Med. 2017 May;13(5):2247-2254. doi: 10.3892/etm.2017.4283. Epub 2017 Mar 29.
Transcranial magnetic stimulation (TMS) is a method of noninvasive brain stimulation that causes neuromodulation by activating neurons or changing excitability in a certain brain area. Considering the known effects of TMS and the pathophysiology of traumatic brain injury (TBI), TMS was proposed to have potential for treating this condition. Moderate TBI was induced in adult male Sprague Dawley rats using Feeney's weight-dropping method. Injured rats were divided into a TMS group and a control group. Repetitive TMS (rTMS) was administered to rats in the TMS group from post-TBI day 2. At post-TBI days 7, 14 and 28, three or four of the rats were sacrificed, and harvested brains were embedded in paraffin and sectioned. Sections were then treated with hematoxylin and eosin and immunohistochemical staining. Three rats from each group underwent fludeoxyglucose F 18 micro-positron emission tomography scanning on post-TBI day 2 and 13. The unexpected mortality rate after injury was lower in the TMS group than in the control group. The modified neurological severity score of the TMS group was lower compared with the control group at post-TBI day 14. According to the results of hematoxylin eosin staining, relative cerebral parenchyma loss was lower at post-TBI day 28 in the TMS group compared with the control group. However, the aforementioned differences were not found to be statistically significant. There was also no significant difference in glucose metabolism between the two groups. According to immunohistochemical staining, the TMS group showed a significantly higher level of proliferation (indicated by bromodeoxyuridine) in the subventricular zone, as compared with the control group (P<0.05). A significantly higher rate of neuron survival at day 28 (P<0.05; indicated by NeuN) and a significantly reduced rate of apoptosis at days 7 and 14 (P<0.05; indicated by caspase-3) were observed in the perilesional zone of the TMS group, as compared with the control group. The current findings suggest that high-frequency rTMS may promote neurogenesis and provide a basis for further studies in this area.
经颅磁刺激(TMS)是一种非侵入性脑刺激方法,通过激活神经元或改变特定脑区的兴奋性来引起神经调节。考虑到TMS的已知作用和创伤性脑损伤(TBI)的病理生理学,有人提出TMS有可能治疗这种疾病。采用Feeney的重物坠落法在成年雄性Sprague Dawley大鼠中诱导中度TBI。将受伤大鼠分为TMS组和对照组。从TBI后第2天开始对TMS组大鼠进行重复经颅磁刺激(rTMS)。在TBI后第7、14和28天,处死3或4只大鼠,将收获的大脑嵌入石蜡并切片。然后对切片进行苏木精和伊红染色以及免疫组织化学染色。每组3只大鼠在TBI后第2天和第13天接受氟脱氧葡萄糖F 18微正电子发射断层扫描。TMS组损伤后的意外死亡率低于对照组。在TBI后第14天,TMS组的改良神经严重程度评分低于对照组。根据苏木精伊红染色结果,与对照组相比,TMS组在TBI后第28天相对脑实质损失较低。然而,上述差异未发现具有统计学意义。两组之间的葡萄糖代谢也没有显著差异。根据免疫组织化学染色,与对照组相比,TMS组在脑室下区显示出显著更高的增殖水平(以溴脱氧尿苷表示)(P<0.05)。与对照组相比,在TMS组的损伤周围区域观察到在第28天神经元存活率显著更高(P<0.05;以NeuN表示),在第7天和第14天细胞凋亡率显著降低(P<0.05;以caspase-3表示)。目前的研究结果表明,高频rTMS可能促进神经发生,并为该领域的进一步研究提供了基础。