对侧阳极经颅直流电刺激促进小鼠皮质脊髓束轴突萌发和脑外伤后的功能恢复

Neurorehabilitation and neural repair Pub Date : 2024-03-01 Epub Date: 2024-02-22 DOI:10.1177/15459683241233261
Beike Chen, Qiang Tan, Hongyan Zhang, Weihua Chu, Huizhong Wen, Xuelong Tian, Yang Yang, Weina Li, Wenyan Li, Yujie Chen, Hua Feng
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引用次数: 0

摘要

背景:阳极经颅直流电刺激(AtDCS)是一种神经调节技术,已被用于治疗创伤性脑损伤(TBI)患者,据报道可促进功能改善。我们在创伤性脑损伤小鼠模型中评估了对侧 AtDCS 对完整皮质脊髓束(CST)轴突萌发的影响及其内在机制,从而为使用 AtDCS 治疗创伤性脑损伤提供更多临床前证据:方法:用挫伤装置诱导小鼠发生 TBI。方法:通过挫伤装置诱发小鼠 TBI,然后对小鼠进行每周 5 天、间隔 2 天的对侧 AtDCS 治疗,持续 7 周。AtDCS 后,通过不规则阶梯行走、窄梁行走和开阔地测试评估运动功能。通过对皮质脊髓神经元(CSNs)进行顺行和逆行标记来评估CST萌发情况,并通过使用氯氮平-氧化物(CNO)对轴突萌发进行药物抑制来进一步验证AtDCS的效果:结果:创伤性脑损伤导致同侧皮层受损,而对侧 CST 保持完好。AtDCS 通过促进 CST 轴突萌发,特别是从完好的半轴到失神经半轴的萌发,改善了 TBI 小鼠受损后肢的熟练运动功能。此外,对CSNs的电刺激显著提高了神经元的兴奋性,从而激活了雷帕霉素机制靶点(mTOR)通路:对侧 AtDCS 改善了创伤性脑损伤后的熟练运动能力,部分原因是通过增加神经元活动促进了轴突萌发,从而激活了 mTOR 通路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Contralesional Anodal Transcranial Direct Current Stimulation Promotes Intact Corticospinal Tract Axonal Sprouting and Functional Recovery After Traumatic Brain Injury in Mice.

Background: Anodal transcranial direct current stimulation (AtDCS), a neuromodulatory technique, has been applied to treat traumatic brain injury (TBI) in patients and was reported to promote functional improvement. We evaluated the effect of contralesional AtDCS on axonal sprouting of the intact corticospinal tract (CST) and the underlying mechanism in a TBI mouse model to provide more preclinical evidence for the use of AtDCS to treat TBI.

Methods: TBI was induced in mice by a contusion device. Then, the mice were subjected to contralesional AtDCS 5 days per week followed by a 2-day interval for 7 weeks. After AtDCS, motor function was evaluated by the irregular ladder walking, narrow beam walking, and open field tests. CST sprouting was assessed by anterograde and retrograde labeling of corticospinal neurons (CSNs), and the effect of AtDCS was further validated by pharmacogenetic inhibition of axonal sprouting using clozapine-N-oxide (CNO).

Results: TBI resulted in damage to the ipsilesional cortex, while the contralesional CST remained intact. AtDCS improved the skilled motor functions of the impaired hindlimb in TBI mice by promoting CST axon sprouting, specifically from the intact hemicord to the denervated hemicord. Furthermore, electrical stimulation of CSNs significantly increased the excitability of neurons and thus activated the mechanistic target of rapamycin (mTOR) pathway.

Conclusions: Contralesional AtDCS improved skilled motor following TBI, partly by promoting axonal sprouting through increased neuronal activity and thus activation of the mTOR pathway.

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