Hsieh Tsung-Hsun, Huang Ying-Zu, Rotenberg Alexander, Pascual-Leone Alvaro, Chiang Yung-Hsiao, Wang Jia-Yi, Chen Jia-Jin J
Graduate Institute of Neural Regenerative Medicine Center for Neurotrauma and Neuroregeneration and Department of Biomedical Engineering and.
Department of Neurology, Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Taipei, Taiwan.
Cereb Cortex. 2015 Jul;25(7):1806-14. doi: 10.1093/cercor/bht421. Epub 2014 Jan 22.
Repetitive magnetic stimulation (rTMS), including theta burst stimulation (TBS), is capable of modulating motor cortical excitability through plasticity-like mechanisms and might have therapeutic potential for Parkinson's disease (PD). An animal model would be helpful for elucidating the mechanism of rTMS that remain unclear and controversial. Here, we have established a TMS model in rat and applied this model to study the impact of substantia nigra dopamine neuron on TBS-induced motor plasticity in PD rats. In parallel with human results, continuous TBS (cTBS) successfully suppressed motor evoked potentials (MEPs), while MEPs increased after intermittent TBS (iTBS) in healthy rats. We then tested the effect of iTBS in early and advanced 6-hydroxydopamine (6-OHDA)-lesioned PD. Moreover, dopaminergic neurons in substantia nigra and rotation behavior were assessed to correlate with the amount of iTBS-induced plasticity. In results, iTBS-induced potentiation was reduced in early PD rats and was absent in advanced PD rats. Such reduction in plasticity strongly correlated with the dopaminergic cell loss and the count of rotation in PD rats. In conclusion, we have established a TMS PD rat model. With the help of this model, we confirmed the loss of domaninergic neurons in substantia nigra resulting in reduced rTMS-induced motor plasticity in PD.
重复磁刺激(rTMS),包括theta爆发刺激(TBS),能够通过类似可塑性的机制调节运动皮质兴奋性,并且可能对帕金森病(PD)具有治疗潜力。动物模型将有助于阐明rTMS尚不清楚且存在争议的机制。在此,我们在大鼠中建立了TMS模型,并应用该模型研究黑质多巴胺能神经元对PD大鼠中TBS诱导的运动可塑性的影响。与人类研究结果一致,在健康大鼠中,连续TBS(cTBS)成功抑制了运动诱发电位(MEP),而间歇性TBS(iTBS)后MEP增加。然后,我们测试了iTBS在早期和晚期6-羟基多巴胺(6-OHDA)损伤的PD大鼠中的作用。此外,评估了黑质中的多巴胺能神经元和旋转行为,以与iTBS诱导的可塑性程度相关联。结果显示,早期PD大鼠中iTBS诱导的增强作用降低,晚期PD大鼠中则不存在这种增强作用。这种可塑性的降低与PD大鼠中多巴胺能细胞的丢失以及旋转次数密切相关。总之,我们建立了一个TMS-PD大鼠模型。借助该模型,我们证实了黑质中多巴胺能神经元的丢失导致PD大鼠中rTMS诱导的运动可塑性降低。