TY - JOUR
T1 - The functional role of post-movement beta oscillations in motor termination
AU - Heinrichs-Graham, Elizabeth
AU - Kurz, Max J.
AU - Gehringer, James E.
AU - Wilson, Tony W.
N1 - Funding Information:
Acknowledgements This work was supported by NIH grant R01 MH103220 (TWW), NSF Grant #1539067 (TWW), a Kinman-Old-field Award for Neurodegenerative Research from the University of Nebraska Medical Center (TWW), and funding from the Nebraska Banker’s Association. The Center for Magnetoencephalography at the University of Nebraska Medical Center was founded through an endowment from an anonymous donor. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors declare no conflicts of interest.
Funding Information:
This work was supported by NIH grant R01 MH103220 (TWW), NSF Grant #1539067 (TWW), a Kinman-Oldfield Award for Neurodegenerative Research from the University of Nebraska Medical Center (TWW), and funding from the Nebraska Banker?s Association. The Center for Magnetoencephalography at the University of Nebraska Medical Center was founded through an endowment from an anonymous donor. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors declare no conflicts of interest.
Publisher Copyright:
© 2017, Springer-Verlag Berlin Heidelberg.
PY - 2017/9/1
Y1 - 2017/9/1
N2 - Shortly after movement termination, there is a strong increase or resynchronization of the beta rhythm (15–30 Hz) across the sensorimotor network of humans, known as the post-movement beta rebound (PMBR). This response has been associated with active inhibition of the motor network following the completion of a movement, sensory afferentation of the sensorimotor cortices, and other functions. However, studies that have directly probed the role of the PMBR in movement execution have reported mixed results, possibly due to differences in the amount of total motor output and/or movement complexity. Herein, we used magnetoencephalography during an isometric-force control task to examine whether alterations in the timing of motor termination demands modulate the PMBR, independent of differences in the motor output itself. Briefly, we manipulated the amount of time between the cue to initiate the force and the cue to terminate the force, such that participants were either forced to terminate quickly or slowly. We also performed a control experiment to test for temporal predictability effects. Our results indicated that the PMBR was stronger immediately following movement termination in the prefrontal cortices, supplementary motor area, left postcentral gyrus, paracentral lobule, and parietal cortex when participants were forced to terminate more quickly. These results were not attributable to the temporal predictability of each condition. These findings support the notion that the PMBR response at least partially serves motor inhibition, independent of the parameters within the motor output itself, and that particular nodes of the motor network may be differentially modulated by motor termination.
AB - Shortly after movement termination, there is a strong increase or resynchronization of the beta rhythm (15–30 Hz) across the sensorimotor network of humans, known as the post-movement beta rebound (PMBR). This response has been associated with active inhibition of the motor network following the completion of a movement, sensory afferentation of the sensorimotor cortices, and other functions. However, studies that have directly probed the role of the PMBR in movement execution have reported mixed results, possibly due to differences in the amount of total motor output and/or movement complexity. Herein, we used magnetoencephalography during an isometric-force control task to examine whether alterations in the timing of motor termination demands modulate the PMBR, independent of differences in the motor output itself. Briefly, we manipulated the amount of time between the cue to initiate the force and the cue to terminate the force, such that participants were either forced to terminate quickly or slowly. We also performed a control experiment to test for temporal predictability effects. Our results indicated that the PMBR was stronger immediately following movement termination in the prefrontal cortices, supplementary motor area, left postcentral gyrus, paracentral lobule, and parietal cortex when participants were forced to terminate more quickly. These results were not attributable to the temporal predictability of each condition. These findings support the notion that the PMBR response at least partially serves motor inhibition, independent of the parameters within the motor output itself, and that particular nodes of the motor network may be differentially modulated by motor termination.
KW - Cortex
KW - MEG
KW - Magnetoencephalography
KW - Movement
KW - PMBR
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U2 - 10.1007/s00429-017-1387-1
DO - 10.1007/s00429-017-1387-1
M3 - Article
C2 - 28337597
AN - SCOPUS:85015904358
SN - 1863-2653
VL - 222
SP - 3075
EP - 3086
JO - Brain Structure and Function
JF - Brain Structure and Function
IS - 7
ER -