Department of Neurology, Goethe-University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany.
J Physiol. 2009 Nov 1;587(Pt 21):5163-76. doi: 10.1113/jphysiol.2009.179820. Epub 2009 Sep 14.
Transcranial magnetic stimulation (TMS) allows the testing of various inhibitory processes in human motor cortex. Here we aimed at gaining more insight into the underlying physiology by studying the interactions between short-interval intracortical inhibition (SICI) and short-latency afferent inhibition (SAI). SICI and SAI were examined in a slightly contracting hand muscle of healthy subjects by measuring inhibition of a test motor-evoked potential conditioned by a sub-threshold motor cortical magnetic pulse (S1) or an electrical pulse (P) applied to the ulnar nerve at the wrist, respectively. SICI alone and SAI alone had similar magnitude when S1 intensity was set to 90% active motor threshold and P intensity to three times the perceptual sensory threshold. SICI was reduced or even disinhibited when P was co-applied, and SAI was reduced or disinhibited when S1 was co-applied. These interactions did not depend on the exact timing of arrival of P and S1 in motor cortex. A control experiment with a S1 intensity lowered to 70% active motor threshold excluded a contribution by short-interval intracortical facilitation. Finally, SICI with co-applied P correlated linearly with SICI alone with a slope of the regression line close to 1 whereas SAI did not correlate with SAI when S1 was co-applied with a slope of the regression line close to zero. Data indicate that S1 largely eliminates the effects of P when applied together, suggesting dominance of S1 over P. Findings strongly support the idea that SICI and SAI are mediated through two distinct and reciprocally connected subtypes of GABAergic inhibitory interneurons with convergent projections onto the corticospinal neurons. Furthermore, dominance of S1 over P is compatible with the notion that the SICI interneurons target the corticospinal neurons closer to their axon initial segment than the SAI interneurons.
经颅磁刺激(TMS)允许在人类运动皮层中测试各种抑制过程。在这里,我们通过研究短程抑制(SICI)和短潜伏期传入抑制(SAI)之间的相互作用,旨在深入了解其潜在的生理学机制。我们通过测量在手腕处施加到尺神经的阈下运动皮质磁脉冲(S1)或电脉冲(P)条件下测试运动诱发电位的抑制,在手的轻度收缩肌肉中检查 SICI 和 SAI。当 S1 强度设置为 90%主动运动阈值,P 强度设置为感知感觉阈值的三倍时,SICI 单独和 SAI 单独的幅度相似。当共同施加 P 时,SICI 减少甚至失抑制,当共同施加 S1 时,SAI 减少或失抑制。这些相互作用不依赖于 P 和 S1 在运动皮层中的到达的确切时间。当 S1 强度降低到 70%主动运动阈值的对照实验排除了短程皮层内易化的贡献。最后,与单独施加 P 的 SICI 呈线性相关,回归线的斜率接近于 1,而当 S1 与 S1 共同施加时,SAI 与 SAI 不相关,回归线的斜率接近于 0。数据表明,当一起施加时,S1 大大消除了 P 的影响,表明 S1 对 P 的主导作用。这些发现强烈支持这样的观点,即 SICI 和 SAI 通过两种不同的、相互连接的 GABA 能抑制性中间神经元亚型介导,它们的投射在皮质脊髓神经元上会聚。此外,S1 对 P 的主导作用与 SICI 中间神经元的靶标更接近皮质脊髓神经元的轴突起始段而不是 SAI 中间神经元的靶标相一致。