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Beta resting-state functional connectivity predicts tactile spatial acuity

Tactile perception is a complex phenomenon that is processed by multiple cortical regions via the primary somatosensory cortex (S1). Although somatosensory gating in the S1 using paired-pulse stimulation can predict tactile performance, the functional relevance of cortico-cortical connections to tac...

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Autores principales: Sasaki, Ryoki, Kojima, Sho, Otsuru, Naofumi, Yokota, Hirotake, Saito, Kei, Shirozu, Hiroshi, Onishi, Hideaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431746/
https://www.ncbi.nlm.nih.gov/pubmed/37344255
http://dx.doi.org/10.1093/cercor/bhad221
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author Sasaki, Ryoki
Kojima, Sho
Otsuru, Naofumi
Yokota, Hirotake
Saito, Kei
Shirozu, Hiroshi
Onishi, Hideaki
author_facet Sasaki, Ryoki
Kojima, Sho
Otsuru, Naofumi
Yokota, Hirotake
Saito, Kei
Shirozu, Hiroshi
Onishi, Hideaki
author_sort Sasaki, Ryoki
collection PubMed
description Tactile perception is a complex phenomenon that is processed by multiple cortical regions via the primary somatosensory cortex (S1). Although somatosensory gating in the S1 using paired-pulse stimulation can predict tactile performance, the functional relevance of cortico-cortical connections to tactile perception remains unclear. We investigated the mechanisms by which corticocortical and local networks predict tactile spatial acuity in 42 adults using magnetoencephalography (MEG). Resting-state MEG was recorded with the eyes open, whereas evoked responses were assessed using single- and paired-pulse electrical stimulation. Source data were used to estimate the S1-seed resting-state functional connectivity (rs-FC) in the whole brain and the evoked response in the S1. Two-point discrimination threshold was assessed using a custom-made device. The beta rs-FC revealed a negative correlation between the discrimination threshold and S1–superior parietal lobule, S1–inferior parietal lobule, and S1–superior temporal gyrus connection (all P < 0.049); strong connectivity was associated with better performance. Somatosensory gating of N20m was also negatively correlated with the discrimination threshold (P = 0.015), with weak gating associated with better performance. This is the first study to demonstrate that specific beta corticocortical networks functionally support tactile spatial acuity as well as the local inhibitory network.
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spelling pubmed-104317462023-08-17 Beta resting-state functional connectivity predicts tactile spatial acuity Sasaki, Ryoki Kojima, Sho Otsuru, Naofumi Yokota, Hirotake Saito, Kei Shirozu, Hiroshi Onishi, Hideaki Cereb Cortex Original Article Tactile perception is a complex phenomenon that is processed by multiple cortical regions via the primary somatosensory cortex (S1). Although somatosensory gating in the S1 using paired-pulse stimulation can predict tactile performance, the functional relevance of cortico-cortical connections to tactile perception remains unclear. We investigated the mechanisms by which corticocortical and local networks predict tactile spatial acuity in 42 adults using magnetoencephalography (MEG). Resting-state MEG was recorded with the eyes open, whereas evoked responses were assessed using single- and paired-pulse electrical stimulation. Source data were used to estimate the S1-seed resting-state functional connectivity (rs-FC) in the whole brain and the evoked response in the S1. Two-point discrimination threshold was assessed using a custom-made device. The beta rs-FC revealed a negative correlation between the discrimination threshold and S1–superior parietal lobule, S1–inferior parietal lobule, and S1–superior temporal gyrus connection (all P < 0.049); strong connectivity was associated with better performance. Somatosensory gating of N20m was also negatively correlated with the discrimination threshold (P = 0.015), with weak gating associated with better performance. This is the first study to demonstrate that specific beta corticocortical networks functionally support tactile spatial acuity as well as the local inhibitory network. Oxford University Press 2023-06-21 /pmc/articles/PMC10431746/ /pubmed/37344255 http://dx.doi.org/10.1093/cercor/bhad221 Text en © The Author(s) 2023. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Sasaki, Ryoki
Kojima, Sho
Otsuru, Naofumi
Yokota, Hirotake
Saito, Kei
Shirozu, Hiroshi
Onishi, Hideaki
Beta resting-state functional connectivity predicts tactile spatial acuity
title Beta resting-state functional connectivity predicts tactile spatial acuity
title_full Beta resting-state functional connectivity predicts tactile spatial acuity
title_fullStr Beta resting-state functional connectivity predicts tactile spatial acuity
title_full_unstemmed Beta resting-state functional connectivity predicts tactile spatial acuity
title_short Beta resting-state functional connectivity predicts tactile spatial acuity
title_sort beta resting-state functional connectivity predicts tactile spatial acuity
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10431746/
https://www.ncbi.nlm.nih.gov/pubmed/37344255
http://dx.doi.org/10.1093/cercor/bhad221
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