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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2023
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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. |
format | Online Article Text |
id | pubmed-10516504 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
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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