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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
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.
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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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