Cargando…
De novo motor learning creates structure in neural activity space that shapes adaptation
Animals can quickly adapt learned movements in response to external perturbations. Motor adaptation is likely influenced by an animal’s existing movement repertoire, but the nature of this influence is unclear. Long-term learning causes lasting changes in neural connectivity which determine the acti...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245862/ https://www.ncbi.nlm.nih.gov/pubmed/37293081 http://dx.doi.org/10.1101/2023.05.23.541925 |
_version_ | 1785054937112117248 |
---|---|
author | Chang, Joanna C. Perich, Matthew G. Miller, Lee E. Gallego, Juan A. Clopath, Claudia |
author_facet | Chang, Joanna C. Perich, Matthew G. Miller, Lee E. Gallego, Juan A. Clopath, Claudia |
author_sort | Chang, Joanna C. |
collection | PubMed |
description | Animals can quickly adapt learned movements in response to external perturbations. Motor adaptation is likely influenced by an animal’s existing movement repertoire, but the nature of this influence is unclear. Long-term learning causes lasting changes in neural connectivity which determine the activity patterns that can be produced. Here, we sought to understand how a neural population’s activity repertoire, acquired through long-term learning, affects short-term adaptation by modeling motor cortical neural population dynamics during de novo learning and subsequent adaptation using recurrent neural networks. We trained these networks on different motor repertoires comprising varying numbers of movements. Networks with multiple movements had more constrained and robust dynamics, which were associated with more defined neural ‘structure’—organization created by the neural population activity patterns corresponding to each movement. This structure facilitated adaptation, but only when small changes in motor output were required, and when the structure of the network inputs, the neural activity space, and the perturbation were congruent. These results highlight trade-offs in skill acquisition and demonstrate how prior experience and external cues during learning can shape the geometrical properties of neural population activity as well as subsequent adaptation. |
format | Online Article Text |
id | pubmed-10245862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-102458622023-06-08 De novo motor learning creates structure in neural activity space that shapes adaptation Chang, Joanna C. Perich, Matthew G. Miller, Lee E. Gallego, Juan A. Clopath, Claudia bioRxiv Article Animals can quickly adapt learned movements in response to external perturbations. Motor adaptation is likely influenced by an animal’s existing movement repertoire, but the nature of this influence is unclear. Long-term learning causes lasting changes in neural connectivity which determine the activity patterns that can be produced. Here, we sought to understand how a neural population’s activity repertoire, acquired through long-term learning, affects short-term adaptation by modeling motor cortical neural population dynamics during de novo learning and subsequent adaptation using recurrent neural networks. We trained these networks on different motor repertoires comprising varying numbers of movements. Networks with multiple movements had more constrained and robust dynamics, which were associated with more defined neural ‘structure’—organization created by the neural population activity patterns corresponding to each movement. This structure facilitated adaptation, but only when small changes in motor output were required, and when the structure of the network inputs, the neural activity space, and the perturbation were congruent. These results highlight trade-offs in skill acquisition and demonstrate how prior experience and external cues during learning can shape the geometrical properties of neural population activity as well as subsequent adaptation. Cold Spring Harbor Laboratory 2023-05-24 /pmc/articles/PMC10245862/ /pubmed/37293081 http://dx.doi.org/10.1101/2023.05.23.541925 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Chang, Joanna C. Perich, Matthew G. Miller, Lee E. Gallego, Juan A. Clopath, Claudia De novo motor learning creates structure in neural activity space that shapes adaptation |
title | De novo motor learning creates structure in neural activity space that shapes adaptation |
title_full | De novo motor learning creates structure in neural activity space that shapes adaptation |
title_fullStr | De novo motor learning creates structure in neural activity space that shapes adaptation |
title_full_unstemmed | De novo motor learning creates structure in neural activity space that shapes adaptation |
title_short | De novo motor learning creates structure in neural activity space that shapes adaptation |
title_sort | de novo motor learning creates structure in neural activity space that shapes adaptation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10245862/ https://www.ncbi.nlm.nih.gov/pubmed/37293081 http://dx.doi.org/10.1101/2023.05.23.541925 |
work_keys_str_mv | AT changjoannac denovomotorlearningcreatesstructureinneuralactivityspacethatshapesadaptation AT perichmatthewg denovomotorlearningcreatesstructureinneuralactivityspacethatshapesadaptation AT millerleee denovomotorlearningcreatesstructureinneuralactivityspacethatshapesadaptation AT gallegojuana denovomotorlearningcreatesstructureinneuralactivityspacethatshapesadaptation AT clopathclaudia denovomotorlearningcreatesstructureinneuralactivityspacethatshapesadaptation |