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Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback

Neuroprosthetics offer great hope for motor-impaired patients. One obstacle is that fine motor control requires near-instantaneous, rich somatosensory feedback. Such distributed feedback may be recreated in a brain-machine interface using distributed artificial stimulation across the cortical surfac...

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Autores principales: Abbasi, Aamir, Lassagne, Henri, Estebanez, Luc, Goueytes, Dorian, Shulz, Daniel E., Ego-Stengel, Valerie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516504/
https://www.ncbi.nlm.nih.gov/pubmed/37738340
http://dx.doi.org/10.1126/sciadv.adh1328
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author Abbasi, Aamir
Lassagne, Henri
Estebanez, Luc
Goueytes, Dorian
Shulz, Daniel E.
Ego-Stengel, Valerie
author_facet Abbasi, Aamir
Lassagne, Henri
Estebanez, Luc
Goueytes, Dorian
Shulz, Daniel E.
Ego-Stengel, Valerie
author_sort Abbasi, Aamir
collection PubMed
description Neuroprosthetics offer great hope for motor-impaired patients. One obstacle is that fine motor control requires near-instantaneous, rich somatosensory feedback. Such distributed feedback may be recreated in a brain-machine interface using distributed artificial stimulation across the cortical surface. Here, we hypothesized that neuronal stimulation must be contiguous in its spatiotemporal dynamics to be efficiently integrated by sensorimotor circuits. Using a closed-loop brain-machine interface, we trained head-fixed mice to control a virtual cursor by modulating the activity of motor cortex neurons. We provided artificial feedback in real time with distributed optogenetic stimulation patterns in the primary somatosensory cortex. Mice developed a specific motor strategy and succeeded to learn the task only when the optogenetic feedback pattern was spatially and temporally contiguous while it moved across the topography of the somatosensory cortex. These results reveal spatiotemporal properties of the sensorimotor cortical integration that set constraints on the design of neuroprosthetics.
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spelling pubmed-105165042023-09-23 Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback Abbasi, Aamir Lassagne, Henri Estebanez, Luc Goueytes, Dorian Shulz, Daniel E. Ego-Stengel, Valerie Sci Adv Neuroscience Neuroprosthetics offer great hope for motor-impaired patients. One obstacle is that fine motor control requires near-instantaneous, rich somatosensory feedback. Such distributed feedback may be recreated in a brain-machine interface using distributed artificial stimulation across the cortical surface. Here, we hypothesized that neuronal stimulation must be contiguous in its spatiotemporal dynamics to be efficiently integrated by sensorimotor circuits. Using a closed-loop brain-machine interface, we trained head-fixed mice to control a virtual cursor by modulating the activity of motor cortex neurons. We provided artificial feedback in real time with distributed optogenetic stimulation patterns in the primary somatosensory cortex. Mice developed a specific motor strategy and succeeded to learn the task only when the optogenetic feedback pattern was spatially and temporally contiguous while it moved across the topography of the somatosensory cortex. These results reveal spatiotemporal properties of the sensorimotor cortical integration that set constraints on the design of neuroprosthetics. American Association for the Advancement of Science 2023-09-22 /pmc/articles/PMC10516504/ /pubmed/37738340 http://dx.doi.org/10.1126/sciadv.adh1328 Text en Copyright © 2023 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution License 4.0 (CC BY). https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution license (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Neuroscience
Abbasi, Aamir
Lassagne, Henri
Estebanez, Luc
Goueytes, Dorian
Shulz, Daniel E.
Ego-Stengel, Valerie
Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title_full Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title_fullStr Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title_full_unstemmed Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title_short Brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
title_sort brain-machine interface learning is facilitated by specific patterning of distributed cortical feedback
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10516504/
https://www.ncbi.nlm.nih.gov/pubmed/37738340
http://dx.doi.org/10.1126/sciadv.adh1328
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