Shulga Anastasia, Lioumis Pantelis, Kirveskari Erika, Savolainen Sarianna, Mäkelä Jyrki P, Ylinen Aarne
Clinical Neurosciences, Neurology, University of Helsinki and Helsinki University Hospital, P.O. Box 372, FI-00029 Helsinki, Finland; BioMag Laboratory, HUS Medical Imaging Center, University of Helsinki and Helsinki University Hospital, P.O. Box 340, FI-00029 Helsinki, Finland.
BioMag Laboratory, HUS Medical Imaging Center, University of Helsinki and Helsinki University Hospital, P.O. Box 340, FI-00029 Helsinki, Finland; Neuroscience Center, University of Helsinki, P.O. Box 56, FI-00014, Finland.
J Neurosci Methods. 2015 Mar 15;242:112-7. doi: 10.1016/j.jneumeth.2015.01.012. Epub 2015 Jan 15.
In spinal paired associative stimulation (PAS), orthodromic volleys are induced by transcranial magnetic stimulation (TMS) in upper motor neurons, and antidromic volleys by peripheral nerve stimulation (PNS) in lower motor neurons of human corticospinal tract. The volleys arriving synchronously to the corticomotoneuronal synapses induce spike time-dependent plasticity in the spinal cord. For clinical use of spinal PAS, it is important to develop protocols that reliably induce facilitation of corticospinal transmission. Due to variability in conductivity of neuronal tracts in neurological patients, it is beneficial to estimate interstimulus interval (ISI) between TMS and PNS on individual basis. Spinal root magnetic stimulation has previously been used for this purpose in spinal PAS targeting upper limbs. However, at lumbar level this method does not take into account the conduction time of spinal nerves of the cauda equina in the spinal canal.
For lower limbs spinal PAS, we propose estimating appropriate ISIs on the basis of F-response and motor-evoked potential (MEP) latencies. The use of navigation in TMS and ensuring correct PNS electrode placement with F-response recording enhances the precision of the method.
Our protocol induced 186±17% (mean±STE) MEP amplitude facilitation in healthy subjects, being effective in all subjects and nerves tested.
We report for the first time the individual estimation of ISIs in spinal PAS for lower limbs.
Estimation of ISI on the basis of F and MEP latencies is sufficient to effectively enhance corticospinal transmission by lower limb spinal PAS in healthy subjects.
在脊髓配对联想刺激(PAS)中,经颅磁刺激(TMS)在上运动神经元中诱发顺行性冲动,而外周神经刺激(PNS)在人类皮质脊髓束的下运动神经元中诱发逆行性冲动。同步到达皮质运动神经元突触的冲动在脊髓中诱导与峰电位时间相关的可塑性。对于脊髓PAS的临床应用,开发能够可靠诱导皮质脊髓传导促进的方案很重要。由于神经疾病患者神经传导束电导率存在变异性,基于个体估计TMS和PNS之间的刺激间隔(ISI)是有益的。脊髓神经根磁刺激此前已用于针对上肢的脊髓PAS。然而,在腰椎水平,这种方法没有考虑马尾神经在椎管内的传导时间。
对于下肢脊髓PAS,我们建议基于F波反应和运动诱发电位(MEP)潜伏期估计合适的ISI。在TMS中使用导航并通过F波反应记录确保PNS电极正确放置可提高该方法的精度。
我们的方案在健康受试者中诱导MEP波幅促进186±17%(平均值±标准误),对所有测试的受试者和神经均有效。
我们首次报告了下肢脊髓PAS中ISI的个体估计。
基于F波反应和MEP潜伏期估计ISI足以通过下肢脊髓PAS有效增强健康受试者的皮质脊髓传导。