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Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex
Transcranial direct current stimulation (tDCS) is a novel intervention that can modulate brain excitability in health and disease; however, little is known about its effects on bilaterally innervated systems such as pharyngeal motor cortex. Here, we assess the effects of differing doses of tDCS on t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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American Physiological Society
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850087/ https://www.ncbi.nlm.nih.gov/pubmed/19815630 http://dx.doi.org/10.1152/ajpgi.00294.2009 |
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author | Jefferson, Samantha Mistry, Satish Singh, Salil Rothwell, John Hamdy, Shaheen |
author_facet | Jefferson, Samantha Mistry, Satish Singh, Salil Rothwell, John Hamdy, Shaheen |
author_sort | Jefferson, Samantha |
collection | PubMed |
description | Transcranial direct current stimulation (tDCS) is a novel intervention that can modulate brain excitability in health and disease; however, little is known about its effects on bilaterally innervated systems such as pharyngeal motor cortex. Here, we assess the effects of differing doses of tDCS on the physiology of healthy human pharyngeal motor cortex as a prelude to designing a therapeutic intervention in dysphagic patients. Healthy subjects (n = 17) underwent seven regimens of tDCS (anodal 10 min 1 mA, cathodal 10 min 1 mA, anodal 10 min 1.5 mA, cathodal 10 min 1.5 mA, anodal 20 min 1 mA, cathodal 20 min 1 mA, Sham) on separate days, in a double blind randomized order. Bihemispheric motor evoked potential (MEP) responses to single-pulse transcranial magnetic stimulation (TMS) as well as intracortical facilitation (ICF) and inhibition (ICI) were recorded using a swallowed pharyngeal catheter before and up to 60 min following the tDCS. Compared with sham, both 10 min 1.5 mA and 20 min 1 mA anodal stimulation induced increases in cortical excitability in the stimulated hemisphere (+44 ± 17% and +59 ± 16%, respectively; P < 0.005) whereas only 10 min 1.5 mA cathodal stimulation induced inhibition (−26 ± 4%, P = 0.02). There were neither contralateral hemisphere changes nor any evidence for ICI or ICF in driving the ipsilateral effects. In conclusion, anodal tDCS can alter pharyngeal motor cortex excitability in an intensity-dependent manner, with little evidence for transcallosal spread. Anodal stimulation may therefore provide a useful means of stimulating pharyngeal cortex and promoting recovery in dysphagic patients. |
format | Text |
id | pubmed-2850087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Physiological Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-28500872010-12-01 Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex Jefferson, Samantha Mistry, Satish Singh, Salil Rothwell, John Hamdy, Shaheen Am J Physiol Gastrointest Liver Physiol Translational Physiology Transcranial direct current stimulation (tDCS) is a novel intervention that can modulate brain excitability in health and disease; however, little is known about its effects on bilaterally innervated systems such as pharyngeal motor cortex. Here, we assess the effects of differing doses of tDCS on the physiology of healthy human pharyngeal motor cortex as a prelude to designing a therapeutic intervention in dysphagic patients. Healthy subjects (n = 17) underwent seven regimens of tDCS (anodal 10 min 1 mA, cathodal 10 min 1 mA, anodal 10 min 1.5 mA, cathodal 10 min 1.5 mA, anodal 20 min 1 mA, cathodal 20 min 1 mA, Sham) on separate days, in a double blind randomized order. Bihemispheric motor evoked potential (MEP) responses to single-pulse transcranial magnetic stimulation (TMS) as well as intracortical facilitation (ICF) and inhibition (ICI) were recorded using a swallowed pharyngeal catheter before and up to 60 min following the tDCS. Compared with sham, both 10 min 1.5 mA and 20 min 1 mA anodal stimulation induced increases in cortical excitability in the stimulated hemisphere (+44 ± 17% and +59 ± 16%, respectively; P < 0.005) whereas only 10 min 1.5 mA cathodal stimulation induced inhibition (−26 ± 4%, P = 0.02). There were neither contralateral hemisphere changes nor any evidence for ICI or ICF in driving the ipsilateral effects. In conclusion, anodal tDCS can alter pharyngeal motor cortex excitability in an intensity-dependent manner, with little evidence for transcallosal spread. Anodal stimulation may therefore provide a useful means of stimulating pharyngeal cortex and promoting recovery in dysphagic patients. American Physiological Society 2009-12 2009-10-01 /pmc/articles/PMC2850087/ /pubmed/19815630 http://dx.doi.org/10.1152/ajpgi.00294.2009 Text en Copyright © 2009 the American Physiological Society This document may be redistributed and reused, subject to www.the-aps.org/publications/journals/funding_addendum_policy.htm (http://www.the-aps.org/publications/journals/funding_addendum_policy.htm) . |
spellingShingle | Translational Physiology Jefferson, Samantha Mistry, Satish Singh, Salil Rothwell, John Hamdy, Shaheen Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title | Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title_full | Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title_fullStr | Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title_full_unstemmed | Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title_short | Characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
title_sort | characterizing the application of transcranial direct current stimulation in human pharyngeal motor cortex |
topic | Translational Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2850087/ https://www.ncbi.nlm.nih.gov/pubmed/19815630 http://dx.doi.org/10.1152/ajpgi.00294.2009 |
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