{"title":"Stable Enhancement of Corticospinal Excitability by the Combination of Paired Associative Stimulation and Interlimb Cortical Network","authors":"Tatsuya Kato, Naotsugu Kaneko, Kimitaka Nakazawa","doi":"10.1111/ejn.70072","DOIUrl":null,"url":null,"abstract":"<p>Inter-individual variability is a common issue of noninvasive brain stimulation. This study aimed to augment neuroplasticity induced by paired associative stimulation (PAS) through leveraging interlimb neural interactions. Specifically, we assessed lower-limb corticospinal excitability when voluntary ipsilateral upper-limb muscle contraction (UMC) was integrated into lower-limb PAS in 19 able-bodied young adults. PAS targeted the right soleus muscle (i.e., a lower-limb muscle), pairing peripheral nerve stimulation (PNS) with transcranial magnetic stimulation (TMS) to modulate cortical excitability. Experiment 1 evaluated motor-evoked potentials (MEPs) and Hoffmann reflex (H-reflex) after PAS + UMC, PAS, and UMC interventions. Experiment 2 investigated the modulation of MEP and short-interval intracortical inhibition (SICI) following PAS + UMC and PAS interventions, with focused attention on PNS. During PAS + UMC intervention, participants performed right wrist flexion at 30% maximum voluntary contraction coinciding with stimulation. Results showed a significant increase in MEPs 30 min after PAS + UMC intervention, with enhanced increase under controlled attention. The H-reflex slightly increased 15 and 30 min after PAS + UMC intervention. SICI increased 30 min after PAS + UMC intervention, though the correlation between MEP and SICI observed in PAS intervention was absent in PAS + UMC intervention. Our findings suggest that combining lower-limb PAS with UMC can facilitate lower-limb corticospinal excitability more effectively than conventional PAS, despite the complex neural mechanism underlying PAS.</p>","PeriodicalId":11993,"journal":{"name":"European Journal of Neuroscience","volume":"61 7","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ejn.70072","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ejn.70072","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Inter-individual variability is a common issue of noninvasive brain stimulation. This study aimed to augment neuroplasticity induced by paired associative stimulation (PAS) through leveraging interlimb neural interactions. Specifically, we assessed lower-limb corticospinal excitability when voluntary ipsilateral upper-limb muscle contraction (UMC) was integrated into lower-limb PAS in 19 able-bodied young adults. PAS targeted the right soleus muscle (i.e., a lower-limb muscle), pairing peripheral nerve stimulation (PNS) with transcranial magnetic stimulation (TMS) to modulate cortical excitability. Experiment 1 evaluated motor-evoked potentials (MEPs) and Hoffmann reflex (H-reflex) after PAS + UMC, PAS, and UMC interventions. Experiment 2 investigated the modulation of MEP and short-interval intracortical inhibition (SICI) following PAS + UMC and PAS interventions, with focused attention on PNS. During PAS + UMC intervention, participants performed right wrist flexion at 30% maximum voluntary contraction coinciding with stimulation. Results showed a significant increase in MEPs 30 min after PAS + UMC intervention, with enhanced increase under controlled attention. The H-reflex slightly increased 15 and 30 min after PAS + UMC intervention. SICI increased 30 min after PAS + UMC intervention, though the correlation between MEP and SICI observed in PAS intervention was absent in PAS + UMC intervention. Our findings suggest that combining lower-limb PAS with UMC can facilitate lower-limb corticospinal excitability more effectively than conventional PAS, despite the complex neural mechanism underlying PAS.
期刊介绍:
EJN is the journal of FENS and supports the international neuroscientific community by publishing original high quality research articles and reviews in all fields of neuroscience. In addition, to engage with issues that are of interest to the science community, we also publish Editorials, Meetings Reports and Neuro-Opinions on topics that are of current interest in the fields of neuroscience research and training in science. We have recently established a series of ‘Profiles of Women in Neuroscience’. Our goal is to provide a vehicle for publications that further the understanding of the structure and function of the nervous system in both health and disease and to provide a vehicle to engage the neuroscience community. As the official journal of FENS, profits from the journal are re-invested in the neuroscientific community through the activities of FENS.