Institute of Clinical Neuroanatomy, Neuroscience Center, Goethe-University Frankfurt, D-60590 Frankfurt/Main, Germany.
J Neurosci. 2012 Nov 28;32(48):17514-23. doi: 10.1523/JNEUROSCI.0409-12.2012.
Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive brain stimulation technique that can alter cortical excitability in human subjects for hours beyond the stimulation period. It thus has potential as a therapeutic tool in neuropsychiatric disorders associated with alterations in cortical excitability. However, rTMS-induced neural plasticity remains insufficiently understood at the cellular level. To learn more about the effects of repetitive magnetic stimulation (rMS), we established an in vitro model of rMS using mouse organotypic entorhino-hippocampal slice cultures. We assessed the outcome of a high-frequency (10 Hz) rMS protocol on functional and structural properties of excitatory synapses in mature hippocampal CA1 pyramidal neurons. Whole-cell patch-clamp recordings, immunohistochemistry, and time-lapse imaging techniques revealed that rMS induces a long-lasting increase in glutamatergic synaptic strength, which is accompanied by structural remodeling of dendritic spines. The effects of rMS on spine size were predominantly seen in small spines, suggesting differential effects of rMS on subpopulations of spines. Furthermore, our data indicate that rMS-induced postsynaptic changes depend on the NMDA receptor-mediated accumulation of GluA1-containing AMPA receptors. These results provide first experimental evidence that rMS induces coordinated functional and structural plasticity of excitatory postsynapses, which is consistent with a long-term potentiation of synaptic transmission.
重复经颅磁刺激(rTMS)是一种非侵入性脑刺激技术,可在刺激期后数小时改变人类受试者的皮质兴奋性。因此,它有可能成为与皮质兴奋性改变相关的神经精神疾病的治疗工具。然而,rTMS 诱导的神经可塑性在细胞水平上仍了解不足。为了更多地了解重复磁刺激(rMS)的影响,我们使用鼠器官型内嗅-海马切片培养物建立了 rMS 的体外模型。我们评估了高频(10 Hz)rMS 方案对成熟海马 CA1 锥体神经元兴奋性突触的功能和结构特性的影响。全细胞膜片钳记录、免疫组织化学和延时成像技术显示,rMS 诱导谷氨酸能突触强度的持久增加,同时伴随着树突棘的结构重塑。rMS 对棘突大小的影响主要见于小棘突,表明 rMS 对棘突亚群有不同的影响。此外,我们的数据表明,rMS 诱导的突触后变化依赖于 NMDA 受体介导的 GluA1 包含的 AMPA 受体的积累。这些结果提供了第一个实验证据,表明 rMS 诱导兴奋性突触的协调性功能和结构可塑性,与突触传递的长时程增强一致。