Decoding hindlimb movement for a brain machine interface after a complete spinal transection.

Stereotypical locomotor movements can be made without input from the brain after a complete spinal transection. However, the restoration of functional gait requires descending modulation of spinal circuits to independently control the movement of each limb. To evaluate whether a brain-machine interf...

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Main Authors: Anitha Manohar, Robert D Flint, Eric Knudsen, Karen A Moxon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3531410?pdf=render
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spelling doaj-9f9d2ed1dde740a8a72433614e550b8d2020-11-25T02:33:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01712e5217310.1371/journal.pone.0052173Decoding hindlimb movement for a brain machine interface after a complete spinal transection.Anitha ManoharRobert D FlintEric KnudsenKaren A MoxonStereotypical locomotor movements can be made without input from the brain after a complete spinal transection. However, the restoration of functional gait requires descending modulation of spinal circuits to independently control the movement of each limb. To evaluate whether a brain-machine interface (BMI) could be used to regain conscious control over the hindlimb, rats were trained to press a pedal and the encoding of hindlimb movement was assessed using a BMI paradigm. Off-line, information encoded by neurons in the hindlimb sensorimotor cortex was assessed. Next neural population functions, or weighted representations of the neuronal activity, were used to replace the hindlimb movement as a trigger for reward in real-time (on-line decoding) in three conditions: while the animal could still press the pedal, after the pedal was removed and after a complete spinal transection. A novel representation of the motor program was learned when the animals used neural control to achieve water reward (e.g. more information was conveyed faster). After complete spinal transection, the ability of these neurons to convey information was reduced by more than 40%. However, this BMI representation was relearned over time despite a persistent reduction in the neuronal firing rate during the task. Therefore, neural control is a general feature of the motor cortex, not restricted to forelimb movements, and can be regained after spinal injury.http://europepmc.org/articles/PMC3531410?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Anitha Manohar
Robert D Flint
Eric Knudsen
Karen A Moxon
spellingShingle Anitha Manohar
Robert D Flint
Eric Knudsen
Karen A Moxon
Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
PLoS ONE
author_facet Anitha Manohar
Robert D Flint
Eric Knudsen
Karen A Moxon
author_sort Anitha Manohar
title Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
title_short Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
title_full Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
title_fullStr Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
title_full_unstemmed Decoding hindlimb movement for a brain machine interface after a complete spinal transection.
title_sort decoding hindlimb movement for a brain machine interface after a complete spinal transection.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Stereotypical locomotor movements can be made without input from the brain after a complete spinal transection. However, the restoration of functional gait requires descending modulation of spinal circuits to independently control the movement of each limb. To evaluate whether a brain-machine interface (BMI) could be used to regain conscious control over the hindlimb, rats were trained to press a pedal and the encoding of hindlimb movement was assessed using a BMI paradigm. Off-line, information encoded by neurons in the hindlimb sensorimotor cortex was assessed. Next neural population functions, or weighted representations of the neuronal activity, were used to replace the hindlimb movement as a trigger for reward in real-time (on-line decoding) in three conditions: while the animal could still press the pedal, after the pedal was removed and after a complete spinal transection. A novel representation of the motor program was learned when the animals used neural control to achieve water reward (e.g. more information was conveyed faster). After complete spinal transection, the ability of these neurons to convey information was reduced by more than 40%. However, this BMI representation was relearned over time despite a persistent reduction in the neuronal firing rate during the task. Therefore, neural control is a general feature of the motor cortex, not restricted to forelimb movements, and can be regained after spinal injury.
url http://europepmc.org/articles/PMC3531410?pdf=render
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