Abstract

The late indirect (I)-waves recruited by transcranial magnetic stimulation (TMS) over primary motor cortex (M1) can be modulated using I-wave periodicity repetitive TMS (iTMS). The purpose of this study was to determine if the response to iTMS is influenced by different interstimulus intervals (ISIs) targeting late I-waves, and whether these responses were associated with individual variations in intracortical excitability. Seventeen young (27.2 ± 6.4 years, 12 females) healthy adults received iTMS at late I-wave intervals (4.0, 4.5, and 5.0 ms) in three separate sessions. Changes due to each intervention were examined with motor evoked potential (MEP) amplitudes and short-interval intracortical facilitation (SICF) using both posterior-anterior (PA) and anterior-posterior (AP) TMS current directions. Changes in MEP amplitude and SICF were influenced by iTMS ISI, with the greatest facilitation for ISIs at 4 and 5 ms with PA TMS, and 4 ms with AP TMS. Maximum SICF at baseline (irrespective of ISI) was associated with increased iTMS response, but only for PA stimulation. These results suggest that modifying iTMS parameters targeting late I-waves can influence M1 plasticity. They also suggest that maximum SICF may be a means by which responders to iTMS targeting the late I-waves could be identified.

Highlights

  • For PA stimulation, facilitation differed between interstimulus intervals (ISIs) (p = 0.04), no significant post hoc differences were found

  • There was no difference between I-wave periodicity repetitive TMS (iTMS) sessions (p = 0.2) or interaction between iTMS sessions and short-interval intracortical facilitation (SICF) ISI (p = 0.9)

  • PA and AP stimulation, the changes observed with each current direction demonstrated differential temporal specificity, with the greatest effects observed for ISIs at 4 and 5 ms with

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Summary

Introduction

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. Transcranial magnetic stimulation (TMS) is a non-invasive brain stimulation technique that has significantly facilitated our ability to investigate human neurophysiology in vivo. TMS remains the only technique able to both induce and measure neuroplastic changes within the brain [1,2]. Neuroplasticity refers to the brains ability to modify its intrinsic structural and functional connectivity and is a process that is heavily implicated in core neurological functions such as generating memories, learning new skills, and recovering from brain damage [3,4,5]. The application of TMS for understanding neuroplasticity is, critical for research in both healthy individuals and clinical populations alike

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