Kukaswadia Sadiya, Wagle-Shukla Aparna, Morgante Francesca, Gunraj Carolyn, Chen Robert
Division of Neurology, Krembil Neuroscience Centre and Toronto Western Research Institute, University Health Network, University of Toronto, Ontario, Canada.
J Physiol. 2005 Mar 15;563(Pt 3):915-24. doi: 10.1113/jphysiol.2004.080010. Epub 2005 Jan 13.
Various inhibitory pathways exist in the human brain which are crucial in modulating motor cortex output and they can be investigated non-invasively using transcranial magnetic stimulation. Interhemispheric inhibition (IHI) is one form of cortical inhibition. It can be elicited by stimulation of the opposite motor cortex at interstimulus intervals (ISIs) of 10 ms (IHI10) or 40 ms (IHI40) and inhibitions at these intervals are probably mediated by different mechanisms. Peripheral sensory stimulation can also inhibit the motor cortex. Median nerve stimulation produces long latency afferent inhibition (LAI) at ISI 200 ms. LAI inhibits another form of cortical inhibition known as long interval intracortical inhibition (LICI) and a study that examined the interaction between IHI10 and LICI hypothesized that they are mediated by an overlapping population of inhibitory neurones. We tested this hypothesis by examining the interaction between IHI10, IHI40 and LAI. With increasing test MEP amplitude LAI, IHI10 and IHI40 all decreased. There was no correlation between the strength of LAI, IHI10 and IHI40. In the presence of LAI, IHI10 was slightly but significantly reduced compared to IHI10 alone. There was no correlation between the reduction in IHI10 in the presence of LAI and the strength of LAI or IHI10. In the presence of LAI, IHI40 was significantly reduced compared to IHI40 alone. LAI produced a greater decrease in IHI40 than in IHI10. The decrease in IHI40 in the presence of LAI strongly correlated with the strength of LAI but not with the strength of IHI40. Reducing the strength of LAI, IHI10 and IHI40 still resulted in similar interaction between IHI10 and LAI but markedly decreased the effect of LAI on IHI40. We conclude that LAI and IHI10 do not directly inhibit each other but LAI probably inhibits IHI40. LICI is more likely to be related to IHI40 than to IHI10.
人类大脑中存在多种抑制通路,这些通路对于调节运动皮层输出至关重要,并且可以使用经颅磁刺激进行非侵入性研究。半球间抑制(IHI)是皮层抑制的一种形式。它可以通过在10毫秒(IHI10)或40毫秒(IHI40)的刺激间隔(ISI)刺激对侧运动皮层来诱发,并且在这些间隔的抑制可能由不同机制介导。外周感觉刺激也可以抑制运动皮层。正中神经刺激在ISI 200毫秒时产生长潜伏期传入抑制(LAI)。LAI抑制另一种形式的皮层抑制,即长间隔皮层内抑制(LICI),一项研究IHI10和LICI之间相互作用的研究假设它们由重叠的抑制性神经元群体介导。我们通过研究IHI10、IHI40和LAI之间的相互作用来检验这一假设。随着测试运动诱发电位(MEP)幅度的增加,LAI、IHI10和IHI40均降低。LAI、IHI10和IHI40的强度之间没有相关性。在存在LAI的情况下,与单独的IHI10相比,IHI10略有但显著降低。在存在LAI的情况下IHI10的降低与LAI或IHI10的强度之间没有相关性。在存在LAI的情况下,与单独的IHI40相比,IHI40显著降低。LAI使IHI40的降低幅度大于IHI10。在存在LAI的情况下IHI40的降低与LAI的强度密切相关,但与IHI40的强度无关。降低LAI、IHI10和IHI40的强度仍然导致IHI10和LAI之间存在类似的相互作用,但显著降低了LAI对IHI40的影响。我们得出结论,LAI和IHI10不会直接相互抑制,但LAI可能抑制IHI40。LICI更可能与IHI40相关而不是与IHI10相关。