Nonlinear coupling between cortical oscillations and muscle activity during isotonic wrist flexion

Nonlinear coupling between cortical oscillations and muscle activity during isotonic wrist flexion

Yang, Y. (TU Delft Biomechatronics & Human-Machine Control)
Solis Escalante, T. (TU Delft Biomechatronics & Human-Machine Control)
van de Ruit, M.L. (TU Delft Biomechatronics & Human-Machine Control)
van der Helm, F.C.T. (TU Delft Biomechatronics & Human-Machine Control)
Schouten, A.C. (TU Delft Biomechatronics & Human-Machine Control)

2016

Coupling between cortical oscillations and muscle activity facilitates neuronal communication during motor control. The linear part of this coupling, known as corticomuscular coherence, has received substantial attention, even though neuronal communication underlying motor control has been demonstrated to be highly nonlinear. A full assessment of corticomuscular coupling, including the nonlinear part, is essential to understand the neuronal communication within the sensorimotor system. In this study, we applied the recently developed n:m coherence method to assess nonlinear corticomuscular coupling during isotonic wrist flexion. The n:m coherence is a generalized metric for quantifying nonlinear cross-frequency coupling as well as linear iso-frequency coupling. By using independent component analysis (ICA) and equivalent current dipole source localization, we identify four sensorimotor related brain areas based on the locations of the dipoles, i.e., the contralateral primary sensorimotor areas, supplementary motor area (SMA), prefrontal area (PFA) and posterior parietal cortex (PPC). For all these areas, linear coupling between electroencephalogram (EEG) and electromyogram (EMG) is present with peaks in the beta band (15–35 Hz), while nonlinear coupling is detected with both integer (1:2, 1:3, 1:4) and non-integer (2:3) harmonics. Significant differences between brain areas is shown in linear coupling with stronger coherence for the primary sensorimotor areas and motor association cortices (SMA, PFA) compared to the sensory association area (PPC); but not for the nonlinear coupling. Moreover, the detected nonlinear coupling is similar to previously reported nonlinear coupling of cortical activity to somatosensory stimuli. We suggest that the descending motor pathways mainly contribute to linear corticomuscular coupling, while nonlinear coupling likely originates from sensory feedback.

corticomuscular coupling
nonlinear coherence
sensorimotor system
EEG
EMG
OA-Fund TU Delft

http://resolver.tudelft.nl/uuid:37498245-e243-4d13-9334-e691628f86ea

https://doi.org/10.3389/fncom.2016.00126

1662-5188

Frontiers in Computational Neuroscience, 10

Institutional Repository

journal article

© 2016 Y. Yang, T. Solis Escalante, M.L. van de Ruit, F.C.T. van der Helm, A.C. Schouten