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人类运动皮层具有高保真时依赖突触可塑性的证据。

Evidence for high-fidelity timing-dependent synaptic plasticity of human motor cortex.

机构信息

Australian Neuro-Muscular Research Institute and Centre for Neuromuscular and Neurological Disorders, University of Western Australia, Nedlands, Australia.

出版信息

J Neurophysiol. 2013 Jan;109(1):106-12. doi: 10.1152/jn.00584.2011. Epub 2012 Oct 17.

Abstract

A single transcranial magnetic stimulation (TMS) pulse typically evokes a short series of spikes in corticospinal neurons [known as indirect (I)-waves] which are thought to arise from transynaptic input. Delivering a second pulse at inter-pulse intervals (IPIs) corresponding to the timing of these I-waves leads to a facilitation of the response, and if stimulus pairs are delivered repeatedly, a persistent LTP-like increase in excitability can occur. This has been demonstrated at an IPI of 1.5 ms, which corresponds to the first I-wave interval, in an intervention referred to as ITMS (I-wave TMS), and it has been argued that this may have similarities with timing-dependent plasticity models. Consequently, we hypothesized that if the second stimulus is delivered so as not to coincide with I-wave timing, it should lead to LTD. We performed a crossover study in 10 subjects in which TMS doublets were timed to coincide (1.5-ms IPI, ITMS(1.5)) or not coincide (2-ms IPI, ITMS(2)) with I-wave firing. Single pulse motor-evoked potential (MEP) amplitude, resting motor threshold (RMT), and short-interval cortical inhibition (SICI) were measured from the first dorsal interosseous (FDI) muscle. After ITMS(1.5) corticomotor excitability was increased by 60% for 15 min (P < 0.05) and returned to baseline by 20 min. Increasing the IPI by just 500 μs to 2 ms reversed the aftereffect, and MEP amplitude was significantly reduced (35%, P < 0.05) for 15 min before returning to baseline. This reduction was not associated with an increase in SICI, suggesting a reduction in excitatory transmission rather than an increase in inhibitory efficacy. RMT also remained unchanged, suggesting that these changes were not due to changes in membrane excitability. Amplitude-matching ITMS(2) did not modulate excitability. The results are consistent with timing-dependent synaptic LTP/D-like effects and suggest that there are plasticity mechanisms operating in the human motor cortex with a temporal resolution of the order of a few hundreds of microseconds.

摘要

单个经颅磁刺激 (TMS) 脉冲通常会在皮质脊髓神经元中引发一系列短的尖峰(称为间接 (I)-波),这些尖峰被认为是由突触间输入引起的。在与这些 I-波的时间相对应的脉冲间间隔 (IPI) 下施加第二个脉冲会导致反应的易化,如果重复施加刺激对,则会发生兴奋性的持续长时程增强 (LTP) 样增加。在干预措施中,在 1.5 毫秒的 IPI 下已经证明了这一点,该 IPI 对应于第一个 I-波间隔,称为 ITMS(I-波 TMS),并且有人认为这可能与时间依赖性可塑性模型具有相似性。因此,我们假设如果第二个刺激施加的时间不与 I-波时间相对应,则应该导致 LTD。我们在 10 名受试者中进行了一项交叉研究,其中 TMS 双脉冲的时间与 I-波发射(1.5 毫秒 IPI,ITMS(1.5))或不重合(2 毫秒 IPI,ITMS(2))。从第一背侧骨间肌 (FDI) 测量单脉冲运动诱发电位 (MEP) 幅度、静息运动阈值 (RMT) 和短间隔皮质抑制 (SICI)。在 ITMS(1.5)后,皮质运动兴奋性增加了约 60%,持续 15 分钟(P < 0.05),并在 20 分钟内恢复到基线。将 IPI 仅增加 500 μs 至 2 ms 即可逆转后效,MEP 幅度在 15 分钟内显着降低(约 35%,P < 0.05),然后恢复到基线。这种减少与 SICI 的增加无关,表明兴奋性传递减少,而不是抑制效能增加。RMT 也保持不变,表明这些变化不是由于膜兴奋性的变化引起的。幅度匹配的 ITMS(2) 不会调节兴奋性。结果与时间依赖性突触 LTP/D 样效应一致,并表明在人类运动皮层中存在具有数百微秒左右时间分辨率的可塑性机制。

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