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Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb
BACKGROUND: Continuous theta burst stimulation (cTBS) is a form of repetitive transcranial magnetic stimulation which has been shown to alter cortical excitability in the upper limb representation of primary somatosensory cortex (SI). However, it is unknown whether cTBS modulates cortical excitabili...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504565/ https://www.ncbi.nlm.nih.gov/pubmed/23113936 http://dx.doi.org/10.1186/1471-2202-13-133 |
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author | Zapallow, Christopher M Asmussen, Michael J Bolton, David A E Lee, Kevin G H Jacobs, Mark F Nelson, Aimee J |
author_facet | Zapallow, Christopher M Asmussen, Michael J Bolton, David A E Lee, Kevin G H Jacobs, Mark F Nelson, Aimee J |
author_sort | Zapallow, Christopher M |
collection | PubMed |
description | BACKGROUND: Continuous theta burst stimulation (cTBS) is a form of repetitive transcranial magnetic stimulation which has been shown to alter cortical excitability in the upper limb representation of primary somatosensory cortex (SI). However, it is unknown whether cTBS modulates cortical excitability within the lower limb representation in SI. The present study investigates the effects of cTBS over the SI lower limb representation on cortical somatosensory evoked potentials (SEPs) and Hoffmann reflex (H-reflex) following tibial nerve stimulation at the knee. SEPs and H-reflex were recorded before and in four time blocks up to 30 minutes following cTBS targeting the lower limb representation within SI. RESULTS: Following cTBS, the P1-N1 first cortical potential was significantly decreased at 12–16 minutes. CTBS also suppressed the P2-N2 second cortical potential for up to 30 minutes following stimulation. The H-reflex remained statistically unchanged following cTBS although there was a modest suppression observed. CONCLUSION: We conclude that cTBS decreases cortical excitability of the lower limb representation of SI as evidenced by suppressed SEP amplitude. The duration and magnitude of the cTBS after effects are similar to those observed in upper limb studies. |
format | Online Article Text |
id | pubmed-3504565 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35045652012-11-23 Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb Zapallow, Christopher M Asmussen, Michael J Bolton, David A E Lee, Kevin G H Jacobs, Mark F Nelson, Aimee J BMC Neurosci Research Article BACKGROUND: Continuous theta burst stimulation (cTBS) is a form of repetitive transcranial magnetic stimulation which has been shown to alter cortical excitability in the upper limb representation of primary somatosensory cortex (SI). However, it is unknown whether cTBS modulates cortical excitability within the lower limb representation in SI. The present study investigates the effects of cTBS over the SI lower limb representation on cortical somatosensory evoked potentials (SEPs) and Hoffmann reflex (H-reflex) following tibial nerve stimulation at the knee. SEPs and H-reflex were recorded before and in four time blocks up to 30 minutes following cTBS targeting the lower limb representation within SI. RESULTS: Following cTBS, the P1-N1 first cortical potential was significantly decreased at 12–16 minutes. CTBS also suppressed the P2-N2 second cortical potential for up to 30 minutes following stimulation. The H-reflex remained statistically unchanged following cTBS although there was a modest suppression observed. CONCLUSION: We conclude that cTBS decreases cortical excitability of the lower limb representation of SI as evidenced by suppressed SEP amplitude. The duration and magnitude of the cTBS after effects are similar to those observed in upper limb studies. BioMed Central 2012-10-31 /pmc/articles/PMC3504565/ /pubmed/23113936 http://dx.doi.org/10.1186/1471-2202-13-133 Text en Copyright ©2012 Zapallow et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Zapallow, Christopher M Asmussen, Michael J Bolton, David A E Lee, Kevin G H Jacobs, Mark F Nelson, Aimee J Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title | Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title_full | Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title_fullStr | Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title_full_unstemmed | Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title_short | Theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
title_sort | theta burst repetitive transcranial magnetic stimulation attenuates somatosensory evoked potentials from the lower limb |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3504565/ https://www.ncbi.nlm.nih.gov/pubmed/23113936 http://dx.doi.org/10.1186/1471-2202-13-133 |
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