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Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement
Correlations between inherent, task-free low-frequency fluctuations in the blood oxygenation level-dependent (BOLD) signals of the brain provide a potent tool to delineate its functional architecture in terms of intrinsic functional connectivity (iFC). Still, it remains unclear how iFC is modulated...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688375/ https://www.ncbi.nlm.nih.gov/pubmed/29230329 http://dx.doi.org/10.1155/2017/5270532 |
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author | Heba, Stefanie Lenz, Melanie Kalisch, Tobias Höffken, Oliver Schweizer, Lauren M. Glaubitz, Benjamin Puts, Nicolaas A. J. Tegenthoff, Martin Dinse, Hubert R. Schmidt-Wilcke, Tobias |
author_facet | Heba, Stefanie Lenz, Melanie Kalisch, Tobias Höffken, Oliver Schweizer, Lauren M. Glaubitz, Benjamin Puts, Nicolaas A. J. Tegenthoff, Martin Dinse, Hubert R. Schmidt-Wilcke, Tobias |
author_sort | Heba, Stefanie |
collection | PubMed |
description | Correlations between inherent, task-free low-frequency fluctuations in the blood oxygenation level-dependent (BOLD) signals of the brain provide a potent tool to delineate its functional architecture in terms of intrinsic functional connectivity (iFC). Still, it remains unclear how iFC is modulated during learning. We employed whole-brain resting-state magnetic resonance imaging prior to and after training-independent repetitive sensory stimulation (rSS), which is known to induce somatosensory cortical reorganization. We investigated which areas in the sensorimotor network are susceptible to neural plasticity (i.e., where changes in functional connectivity occurred) and where iFC might be indicative of enhanced tactile performance. We hypothesized iFC to increase in those brain regions primarily receiving the afferent tactile input. Strengthened intrinsic connectivity within the sensorimotor network after rSS was found not only in the postcentral gyrus contralateral to the stimulated hand, but also in associative brain regions, where iFC correlated positively with tactile performance or learning. We also observed that rSS led to attenuation of the network at higher cortical levels, which possibly promotes facilitation of tactile discrimination. We found that resting-state BOLD fluctuations are linked to behavioral performance and sensory learning, indicating that network fluctuations at rest are predictive of behavioral changes and neuroplasticity. |
format | Online Article Text |
id | pubmed-5688375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-56883752017-12-11 Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement Heba, Stefanie Lenz, Melanie Kalisch, Tobias Höffken, Oliver Schweizer, Lauren M. Glaubitz, Benjamin Puts, Nicolaas A. J. Tegenthoff, Martin Dinse, Hubert R. Schmidt-Wilcke, Tobias Neural Plast Research Article Correlations between inherent, task-free low-frequency fluctuations in the blood oxygenation level-dependent (BOLD) signals of the brain provide a potent tool to delineate its functional architecture in terms of intrinsic functional connectivity (iFC). Still, it remains unclear how iFC is modulated during learning. We employed whole-brain resting-state magnetic resonance imaging prior to and after training-independent repetitive sensory stimulation (rSS), which is known to induce somatosensory cortical reorganization. We investigated which areas in the sensorimotor network are susceptible to neural plasticity (i.e., where changes in functional connectivity occurred) and where iFC might be indicative of enhanced tactile performance. We hypothesized iFC to increase in those brain regions primarily receiving the afferent tactile input. Strengthened intrinsic connectivity within the sensorimotor network after rSS was found not only in the postcentral gyrus contralateral to the stimulated hand, but also in associative brain regions, where iFC correlated positively with tactile performance or learning. We also observed that rSS led to attenuation of the network at higher cortical levels, which possibly promotes facilitation of tactile discrimination. We found that resting-state BOLD fluctuations are linked to behavioral performance and sensory learning, indicating that network fluctuations at rest are predictive of behavioral changes and neuroplasticity. Hindawi 2017 2017-11-02 /pmc/articles/PMC5688375/ /pubmed/29230329 http://dx.doi.org/10.1155/2017/5270532 Text en Copyright © 2017 Stefanie Heba et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Heba, Stefanie Lenz, Melanie Kalisch, Tobias Höffken, Oliver Schweizer, Lauren M. Glaubitz, Benjamin Puts, Nicolaas A. J. Tegenthoff, Martin Dinse, Hubert R. Schmidt-Wilcke, Tobias Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title | Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title_full | Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title_fullStr | Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title_full_unstemmed | Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title_short | Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement |
title_sort | regionally specific regulation of sensorimotor network connectivity following tactile improvement |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688375/ https://www.ncbi.nlm.nih.gov/pubmed/29230329 http://dx.doi.org/10.1155/2017/5270532 |
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