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运动皮层 I 波易化的抑制和去抑制效应。

Inhibitory and disinhibitory effects on I-wave facilitation in motor cortex.

机构信息

Centre for Neuromuscular and Neurological Disorders, M518, University of Western Australia, 35 Stirling Highway, Crawley WA 6009, Perth, Australia.

出版信息

J Neurophysiol. 2011 Jan;105(1):100-6. doi: 10.1152/jn.00650.2010. Epub 2010 Oct 13.

Abstract

A suprathreshold pulse of transcranial magnetic stimulation (TMS) delivered to human motor cortex results in a period of long-interval intracortical inhibition (LICI) followed by a briefer period of disinhibition (late cortical disinhibition [LCD]). Short-interval intracortical facilitation (SICF) is mediated by excitatory networks in the motor cortex responsible for the generation of the indirect (I-) wave volleys that are evoked by TMS at a periodicity of about 1.5 ms. Because the excitatory synaptic network responsible for SICF undergoes inhibitory regulation, we hypothesized that SICF will be modulated during periods of inhibition and disinhibition. In particular we were interested to know whether SICF was up-regulated during disinhibition, implying an increase in excitatory synaptic efficacy. We measured SICF, at a paired-pulse interval of 1.5 ms, at various times (100-300 ms) after a suprathreshold priming stimulus (PS) of sufficient strength to evoke LICI and LCD. We found that the strength of SICF was normal during LICI, but was increased during LCD by an average of 64%. SICF onset latency was reduced by one I-wave interval during LCD and was delayed by one I-wave interval during LICI. We conclude that disinhibition, rather than inhibition, modulates the excitatory neuronal networks that underlie SICF, whereas the I-wave targeted is modified by the presence of both inhibition and disinhibition and that there is therefore a dissociation between the strength and site of SICF interaction. The increase in SICF during disinhibition further indicates that this is a promising period to investigate or modulate excitatory synaptic networks while they are less constrained by ongoing levels of inhibition.

摘要

经颅磁刺激(TMS)施加于人运动皮层的阈上脉冲会导致长时程皮质内抑制(LICI),随后是短暂的去抑制(晚期皮质去抑制[LCD])。短程皮质内易化(SICF)由运动皮层中的兴奋性网络介导,这些网络负责产生 TMS 在约 1.5 ms 的周期性下引发的间接(I-)波。由于负责 SICF 的兴奋性突触网络受到抑制性调节,我们假设 SICF 将在抑制和去抑制期间被调节。特别是,我们感兴趣的是 SICF 是否在去抑制期间上调,这意味着兴奋性突触效能增加。我们在足以引发 LICI 和 LCD 的阈上启动刺激(PS)后,在各种时间(100-300 ms)测量了 1.5 ms 时的 SICF。我们发现 SICF 在 LICI 期间强度正常,但在 LCD 期间平均增加了 64%。在 LCD 期间,SICF 的起始潜伏期减少了一个 I 波间隔,在 LICI 期间延迟了一个 I 波间隔。我们得出结论,去抑制而不是抑制调节了基础 SICF 的兴奋性神经元网络,而被靶向的 I 波则受抑制和去抑制的共同影响而改变,因此 SICF 相互作用的强度和部位存在分离。在去抑制期间 SICF 的增加进一步表明,这是一个有希望的时期,可以在兴奋性突触网络受到抑制的限制较少时研究或调节它们。

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