TY - JOUR
T1 - Regionally Specific Regulation of Sensorimotor Network Connectivity Following Tactile Improvement
AU - Heba, Stefanie
AU - Lenz, Melanie
AU - Kalisch, Tobias
AU - Höffken, Oliver
AU - Schweizer, Lauren M.
AU - Glaubitz, Benjamin
AU - Puts, Nicolaas A.J.
AU - Tegenthoff, Martin
AU - Dinse, Hubert R.
AU - Schmidt-Wilcke, Tobias
N1 - Funding Information:
This work was funded by the Deutsche Forschungsge-meinschaft (SFB874-A1 to Martin Tegenthoff, Melanie Lenz, and Oliver Höffken, SFB874-A5 to Hubert R. Dinse, and SFB874-A8 to Tobias Schmidt-Wilcke; DFG Research Unit 1581 to Benjamin Glaubitz and Martin Tegenthoff); the Ruhr-University Bochum (BoNeuroMed to Lauren M. Schweizer; FORUM-F767-12 to Tobias Kalisch); the Mercator Research Center Ruhr (MERCURE; Pr-2010-0017 to Martin Tegenthoff, Hubert R. Dinse, and Melanie Lenz); and the National Institutes of Health (P41 EB015909, R01 EB016089, R21 MH098228, and K99 MH107719 to Nicolaas A. J. Puts). The authors appreciate the continuous scientific support of PHILIPS Germany.
Publisher Copyright:
© 2017 Stefanie Heba et al.
PY - 2017
Y1 - 2017
N2 - 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.
AB - 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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U2 - 10.1155/2017/5270532
DO - 10.1155/2017/5270532
M3 - Article
C2 - 29230329
AN - SCOPUS:85042444226
SN - 2090-5904
VL - 2017
JO - Neural Plasticity
JF - Neural Plasticity
M1 - 5270532
ER -