Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Manohar, Anitha, Flint, Robert D., Knudsen, Eric, Moxon, Karen A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531410/
https://www.ncbi.nlm.nih.gov/pubmed/23300606
http://dx.doi.org/10.1371/journal.pone.0052173
_version_ 1782254172852191232
author Manohar, Anitha
Flint, Robert D.
Knudsen, Eric
Moxon, Karen A.
author_facet Manohar, Anitha
Flint, Robert D.
Knudsen, Eric
Moxon, Karen A.
author_sort Manohar, Anitha
collection PubMed
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.
format Online
Article
Text
id pubmed-3531410
institution National Center for Biotechnology Information
language English
publishDate 2012
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-35314102013-01-08 Decoding Hindlimb Movement for a Brain Machine Interface after a Complete Spinal Transection Manohar, Anitha Flint, Robert D. Knudsen, Eric Moxon, Karen A. PLoS One Research Article 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. Public Library of Science 2012-12-27 /pmc/articles/PMC3531410/ /pubmed/23300606 http://dx.doi.org/10.1371/journal.pone.0052173 Text en © 2012 Manohar et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Manohar, Anitha
Flint, Robert D.
Knudsen, Eric
Moxon, Karen A.
Decoding Hindlimb Movement for a Brain Machine Interface after a Complete Spinal Transection
title 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_short 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
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3531410/
https://www.ncbi.nlm.nih.gov/pubmed/23300606
http://dx.doi.org/10.1371/journal.pone.0052173
work_keys_str_mv AT manoharanitha decodinghindlimbmovementforabrainmachineinterfaceafteracompletespinaltransection
AT flintrobertd decodinghindlimbmovementforabrainmachineinterfaceafteracompletespinaltransection
AT knudseneric decodinghindlimbmovementforabrainmachineinterfaceafteracompletespinaltransection
AT moxonkarena decodinghindlimbmovementforabrainmachineinterfaceafteracompletespinaltransection