Rizzo V, Mastroeni C, Maggio R, Terranova C, Girlanda P, Siebner H R, Quartarone A
Department of Clinical and Experimental Medicine, University of Messina, Italy.
Department of Clinical and Experimental Medicine, University of Messina, Italy.
Clin Neurophysiol. 2020 Oct;131(10):2402-2409. doi: 10.1016/j.clinph.2020.06.033. Epub 2020 Aug 6.
Sub-motor threshold 5 Hz repetitive paired associative stimulation (5 Hz-rPAS) produces a long-lasting increase in corticospinal excitability. Assuming a spike-timing dependent plasticity-like (STDP-like) mechanism, we hypothesized that 5 Hz-rPAS at a shorter inter-stimulus interval (ISI) of 15 ms (5 Hz-rPAS) would exert a lasting inhibitory effect on corticospinal excitability.
20 healthy volunteers received two minutes of 5 Hz-rPAS. Transcranial magnetic stimulation (TMS) was applied over the motor hotspot of the right abductor pollicis brevis muscle at 90% active motor threshold. Sub-motor threshold peripheral electrical stimulation was given to the left median nerve 15 ms before each TMS pulse. We assessed changes in mean amplitude of the unconditioned motor evoked potential (MEP), short-latency intracortical inhibition (SICI), intracortical facilitation (ICF), short-latency afferent inhibition (SAI), long-latency afferent inhibition (LAI), and cortical silent period (CSP) before and for 60 minutes after 5-Hz rPAS.
Subthreshold 5-Hz rPAS produced a 20-40% decrease in mean MEP amplitude along with an attenuation in SAI, lasting at least 60 minutes. A follow-up experiment revealed that MEP facilitation was spatially restricted to the target muscle.
Subthreshold 5-Hz rPAS effectively suppresses corticospinal excitability. Together with the facilitatory effects of subthreshold 5-Hz rPAS (Quartarone et al., J Physiol 2006;575:657-670), the results show that sub-motor threshold 5-Hz rPAS induces STDP-like bidirectional plasticity in the motor cortex.
The results of the present study provide a new short-time paradigm of long term depression (LTD) induction in human sensory-motor cortex.
阈下5赫兹重复配对联想刺激(5Hz-rPAS)可使皮质脊髓兴奋性产生持久增强。假设存在一种依赖于动作电位发放时间的类可塑性机制(类STDP机制),我们推测,在15毫秒的较短刺激间隔(ISI)下进行5Hz-rPAS(5Hz-rPAS15ms)会对皮质脊髓兴奋性产生持久抑制作用。
20名健康志愿者接受了两分钟的5Hz-rPAS。在右侧拇短展肌运动热点处以90%的主动运动阈值施加经颅磁刺激(TMS)。在每次TMS脉冲前15毫秒,对左侧正中神经给予阈下外周电刺激。我们评估了在5Hz-rPAS之前及之后60分钟内,非条件运动诱发电位(MEP)的平均波幅、短潜伏期皮质内抑制(SICI)、皮质内易化(ICF)、短潜伏期传入抑制(SAI)、长潜伏期传入抑制(LAI)以及皮质静息期(CSP)的变化。
阈下5Hz-rPAS使MEP平均波幅降低了20%至40%,同时SAI减弱,且至少持续60分钟。一项后续实验表明,MEP易化在空间上局限于目标肌肉。
阈下5Hz-rPAS可有效抑制皮质脊髓兴奋性。结合阈下5Hz-rPAS的易化作用(Quartarone等人,《生理学杂志》2006年;575:657 - 670),结果表明阈下5Hz-rPAS在运动皮层诱导了类STDP双向可塑性。
本研究结果为人类感觉运动皮层中长时程抑制(LTD)诱导提供了一种新的短时程模式。