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Augmenting Plasticity Induction in Human Motor Cortex by Disinhibition Stimulation

机译:通过抑制抑制刺激增强人运动皮层的可塑性诱导。

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摘要

Cellular studies showed that disinhibition, evoked pharmacologically or by a suitably timed priming stimulus, can augment long-term plasticity (LTP) induction. We demonstrated previously that transcranial magnetic stimulation evokes a period of presumably GABABergic late cortical disinhibition (LCD) in human primary motor cortex (M1). Here, we hypothesized that, in keeping with cellular studies, LCD can augment LTP-like plasticity in humans. In Experiment 1, patterned repetitive TMS was applied to left M1, consisting of 6 trains (intertrain interval, 8 s) of 4 doublets (interpulse interval equal to individual peak I-wave facilitation, 1.3–1.5 ms) spaced by the individual peak LCD (interdoublet interval (IDI), 200–250 ms). This intervention (total of 48 pulses applied over ∼45 s) increased motor-evoked potential amplitude, a marker of corticospinal excitability, in a right hand muscle by 147% ± 4%. Control experiments showed that IDIs shorter or longer than LCD did not result in LTP-like plasticity. Experiment 2 indicated topographic specificity to the M1 hand region stimulated by TMS and duration of the LTP-like plasticity of 60 min. In conclusion, GABABergic LCD offers a powerful new approach for augmenting LTP-like plasticity induction in human cortex. We refer to this protocol as disinhibition stimulation (DIS).
机译:细胞研究表明,通过药理学或通过适当的定时启动刺激引起的抑制作用可以增强长期可塑性(LTP)诱导。先前我们证明了经颅磁刺激在人类初级运动皮层(M1)中引起了一段时间的GABA能性晚期皮质去抑制(LCD)。在这里,我们假设,根据细胞研究,LCD可以增强人类LTP样可塑性。在实验1中,图案化的重复TMS应用于左M1,由6个列车(列车间隔,8 s)和4个双峰(脉冲间隔等于单个峰值I波促进,1.3-1.5 ms)组成,由单个峰值LCD隔开(间隔间隔(IDI),200-250毫秒)。这种干预(在约45 s内总共施加48个脉冲)使右手肌肉中的运动诱发电位振幅(皮质脊髓兴奋性的标志)增加了147%±4%。对照实验表明,IDI比LCD短或长不会导致类似LTP的可塑性。实验2表明了TMS刺激的M1手区域的地形特异性,LTP样可塑性持续时间为60分钟。总之,GABABergic LCD提供了一种强大的新方法,可增强人类皮质中类似LTP的可塑性诱导。我们将此协议称为去抑制刺激(DIS)。

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