Adam Fry
Modulation of post-movement beta rebound by contraction force and rate of force development
Fry, Adam; Mullinger, Karen J.; O'Neill, George C.; Barratt, Eleanor L.; Morris, Peter G.; Bauer, Markus; Folland, Jonathan P.; Brookes, Matthew J.
Authors
Dr KAREN MULLINGER KAREN.MULLINGER@NOTTINGHAM.AC.UK
ASSOCIATE PROFESSOR
George C. O'Neill
Eleanor L. Barratt
Peter G. Morris
Dr MARKUS BAUER MARKUS.BAUER@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR
Jonathan P. Folland
Professor MATTHEW BROOKES MATTHEW.BROOKES@NOTTINGHAM.AC.UK
PROFESSOR OF PHYSICS
Abstract
Movement induced modulation of the beta rhythm is one of the most robust neural oscillatory phenomena in the brain. In the preparation and execution phases of movement, a loss in beta amplitude is observed (movement related beta decrease (MRBD)). This is followed by a rebound above baseline on movement cessation (post movement beta rebound (PMBR)). These effects have been measured widely, and recent
work suggests that they may have significant importance. Specifically, they have potential to form the basis of biomarkers for disease, and have been used in neuroscience applications ranging from brain computer interfaces to markers of neural plasticity. However, despite the robust nature of both MRBD and PMBR, the phenomena themselves are poorly understood. In this study, we characterise MRBD and PMBR during a carefully controlled isometric wrist flexion paradigm, isolating two fundamental movement parameters;
force output, and the rate of force development (RFD). Our results show that neither altered force output nor RFD has a significant effect on MRBD. In contrast, PMBR was altered by both parameters. Higher force output results in greater PMBR amplitude, and greater RFD results in a PMBR which is higher in amplitude and shorter in duration. These findings demonstrate that careful control of movement parameters can
systematically change PMBR. Further, for temporally protracted movements, the PMBR can be over 7 s in duration. This means accurate control of movement and judicious selection of paradigm parameters are critical in future clinical and basic neuroscientific studies of sensorimotor beta oscillations.
Citation
Fry, A., Mullinger, K. J., O'Neill, G. C., Barratt, E. L., Morris, P. G., Bauer, M., Folland, J. P., & Brookes, M. J. (2016). Modulation of post-movement beta rebound by contraction force and rate of force development. Human Brain Mapping, 37(7), https://doi.org/10.1002/hbm.23189
Journal Article Type | Article |
---|---|
Acceptance Date | Mar 9, 2016 |
Publication Date | Apr 8, 2016 |
Deposit Date | Jan 4, 2017 |
Publicly Available Date | Jan 4, 2017 |
Journal | Human Brain Mapping |
Print ISSN | 1065-9471 |
Electronic ISSN | 1097-0193 |
Publisher | Wiley |
Peer Reviewed | Peer Reviewed |
Volume | 37 |
Issue | 7 |
DOI | https://doi.org/10.1002/hbm.23189 |
Keywords | Neural oscillations; Sensorimotor cortex; Event-related synchronization; Event-related desynchronization; Movement-related beta decrease; Post movement beta rebound; Magnetoencephalography; MEG |
Public URL | https://nottingham-repository.worktribe.com/output/785873 |
Publisher URL | http://onlinelibrary.wiley.com/doi/10.1002/hbm.23189/full |
Contract Date | Jan 4, 2017 |
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Copyright Statement
Copyright information regarding this work can be found at the following address: http://creativecommons.org/licenses/by/4.0
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