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Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation

BACKGROUND: Anodal transcranial direct current stimulation (tDCS) of the somatosensory cortex causes cerebral hyperexcitability and a significant enhancement in pain thresholds and tactile spatial acuity. Sensory gating is a brain mechanism to suppress irrelevant incoming inputs, which is elicited b...

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Autores principales: Montoro, Casandra I., Winterholler, Christine, Terrasa, Juan L., Montoya, Pedro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452934/
https://www.ncbi.nlm.nih.gov/pubmed/34557064
http://dx.doi.org/10.3389/fnins.2021.651253
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author Montoro, Casandra I.
Winterholler, Christine
Terrasa, Juan L.
Montoya, Pedro
author_facet Montoro, Casandra I.
Winterholler, Christine
Terrasa, Juan L.
Montoya, Pedro
author_sort Montoro, Casandra I.
collection PubMed
description BACKGROUND: Anodal transcranial direct current stimulation (tDCS) of the somatosensory cortex causes cerebral hyperexcitability and a significant enhancement in pain thresholds and tactile spatial acuity. Sensory gating is a brain mechanism to suppress irrelevant incoming inputs, which is elicited by presenting pairs of identical stimuli (S1 and S2) within short time intervals between stimuli (e.g., 500 ms). OBJECTIVES/HYPOTHESIS: The present study addressed the question of whether tDCS could modulate the brain correlates of this inhibitory mechanism. METHODS: Forty-one healthy individuals aged 18–26 years participated in the study and were randomly assigned to tDCS (n = 21) or SHAM (n = 20). Somatosensory evoked potentials (SEP) elicited by S1 and S2 pneumatic stimuli (duration of 100 ms, ISI 550 ± 50 ms) and applied to the index finger of the dominant hand were recorded before and after tDCS. RESULTS: Before the intervention, the second tactile stimuli significantly attenuated the amplitudes of P50, N100, and the late positive complex (LPC, mean amplitude in the time window 150–350) compared to the first stimuli. This confirmed that sensory gating is a widespread brain inhibitory mechanism that can affect early- and middle-latency components of SEPs. Furthermore, our data revealed that this response attenuation or sensory gating (computed as S1 minus S2) was improved after tDCS for LPC, while no changes were found in participants who received SHAM. CONCLUSION: All these findings suggested that anodal tDCS might modulate brain excitability leading to an enhancement of inhibitory mechanisms elicited in response to repetitive somatosensory stimuli during late stages of information processing.
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spelling pubmed-84529342021-09-22 Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation Montoro, Casandra I. Winterholler, Christine Terrasa, Juan L. Montoya, Pedro Front Neurosci Neuroscience BACKGROUND: Anodal transcranial direct current stimulation (tDCS) of the somatosensory cortex causes cerebral hyperexcitability and a significant enhancement in pain thresholds and tactile spatial acuity. Sensory gating is a brain mechanism to suppress irrelevant incoming inputs, which is elicited by presenting pairs of identical stimuli (S1 and S2) within short time intervals between stimuli (e.g., 500 ms). OBJECTIVES/HYPOTHESIS: The present study addressed the question of whether tDCS could modulate the brain correlates of this inhibitory mechanism. METHODS: Forty-one healthy individuals aged 18–26 years participated in the study and were randomly assigned to tDCS (n = 21) or SHAM (n = 20). Somatosensory evoked potentials (SEP) elicited by S1 and S2 pneumatic stimuli (duration of 100 ms, ISI 550 ± 50 ms) and applied to the index finger of the dominant hand were recorded before and after tDCS. RESULTS: Before the intervention, the second tactile stimuli significantly attenuated the amplitudes of P50, N100, and the late positive complex (LPC, mean amplitude in the time window 150–350) compared to the first stimuli. This confirmed that sensory gating is a widespread brain inhibitory mechanism that can affect early- and middle-latency components of SEPs. Furthermore, our data revealed that this response attenuation or sensory gating (computed as S1 minus S2) was improved after tDCS for LPC, while no changes were found in participants who received SHAM. CONCLUSION: All these findings suggested that anodal tDCS might modulate brain excitability leading to an enhancement of inhibitory mechanisms elicited in response to repetitive somatosensory stimuli during late stages of information processing. Frontiers Media S.A. 2021-09-07 /pmc/articles/PMC8452934/ /pubmed/34557064 http://dx.doi.org/10.3389/fnins.2021.651253 Text en Copyright © 2021 Montoro, Winterholler, Terrasa and Montoya. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Montoro, Casandra I.
Winterholler, Christine
Terrasa, Juan L.
Montoya, Pedro
Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title_full Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title_fullStr Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title_full_unstemmed Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title_short Somatosensory Gating Is Modulated by Anodal Transcranial Direct Current Stimulation
title_sort somatosensory gating is modulated by anodal transcranial direct current stimulation
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8452934/
https://www.ncbi.nlm.nih.gov/pubmed/34557064
http://dx.doi.org/10.3389/fnins.2021.651253
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