Cargando…
The Bcm rule allows a spinal cord model to learn rhythmic movements
Currently, it is accepted that animal locomotion is controlled by a central pattern generator in the spinal cord. Experiments and models show that rhythm generating neurons and genetically determined network properties could sustain oscillatory output activity suitable for locomotion. However, curre...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600281/ https://www.ncbi.nlm.nih.gov/pubmed/37594531 http://dx.doi.org/10.1007/s00422-023-00970-z |
_version_ | 1785125957523210240 |
---|---|
author | Kohler, Matthias Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik |
author_facet | Kohler, Matthias Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik |
author_sort | Kohler, Matthias |
collection | PubMed |
description | Currently, it is accepted that animal locomotion is controlled by a central pattern generator in the spinal cord. Experiments and models show that rhythm generating neurons and genetically determined network properties could sustain oscillatory output activity suitable for locomotion. However, current central pattern generator models do not explain how a spinal cord circuitry, which has the same basic genetic plan across species, can adapt to control the different biomechanical properties and locomotion patterns existing in these species. Here we demonstrate that rhythmic and alternating movements in pendulum models can be learned by a monolayer spinal cord circuitry model using the Bienenstock–Cooper–Munro learning rule, which has been previously proposed to explain learning in the visual cortex. These results provide an alternative theory to central pattern generator models, because rhythm generating neurons and genetically defined connectivity are not required in our model. Though our results are not in contradiction to current models, as existing neural mechanism and structures, not used in our model, can be expected to facilitate the kind of learning demonstrated here. Therefore, our model could be used to augment existing models. |
format | Online Article Text |
id | pubmed-10600281 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-106002812023-10-27 The Bcm rule allows a spinal cord model to learn rhythmic movements Kohler, Matthias Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik Biol Cybern Original Article Currently, it is accepted that animal locomotion is controlled by a central pattern generator in the spinal cord. Experiments and models show that rhythm generating neurons and genetically determined network properties could sustain oscillatory output activity suitable for locomotion. However, current central pattern generator models do not explain how a spinal cord circuitry, which has the same basic genetic plan across species, can adapt to control the different biomechanical properties and locomotion patterns existing in these species. Here we demonstrate that rhythmic and alternating movements in pendulum models can be learned by a monolayer spinal cord circuitry model using the Bienenstock–Cooper–Munro learning rule, which has been previously proposed to explain learning in the visual cortex. These results provide an alternative theory to central pattern generator models, because rhythm generating neurons and genetically defined connectivity are not required in our model. Though our results are not in contradiction to current models, as existing neural mechanism and structures, not used in our model, can be expected to facilitate the kind of learning demonstrated here. Therefore, our model could be used to augment existing models. Springer Berlin Heidelberg 2023-08-18 2023 /pmc/articles/PMC10600281/ /pubmed/37594531 http://dx.doi.org/10.1007/s00422-023-00970-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Kohler, Matthias Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik The Bcm rule allows a spinal cord model to learn rhythmic movements |
title | The Bcm rule allows a spinal cord model to learn rhythmic movements |
title_full | The Bcm rule allows a spinal cord model to learn rhythmic movements |
title_fullStr | The Bcm rule allows a spinal cord model to learn rhythmic movements |
title_full_unstemmed | The Bcm rule allows a spinal cord model to learn rhythmic movements |
title_short | The Bcm rule allows a spinal cord model to learn rhythmic movements |
title_sort | bcm rule allows a spinal cord model to learn rhythmic movements |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10600281/ https://www.ncbi.nlm.nih.gov/pubmed/37594531 http://dx.doi.org/10.1007/s00422-023-00970-z |
work_keys_str_mv | AT kohlermatthias thebcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT rohrbeinflorian thebcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT knollalois thebcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT albuschafferalin thebcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT jorntellhenrik thebcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT kohlermatthias bcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT rohrbeinflorian bcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT knollalois bcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT albuschafferalin bcmruleallowsaspinalcordmodeltolearnrhythmicmovements AT jorntellhenrik bcmruleallowsaspinalcordmodeltolearnrhythmicmovements |