Cargando…
Coupling between motor cortex and striatum increases during sleep over long-term skill learning
The strength of cortical connectivity to the striatum influences the balance between behavioral variability and stability. Learning to consistently produce a skilled action requires plasticity in corticostriatal connectivity associated with repeated training of the action. However, it remains unknow...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439654/ https://www.ncbi.nlm.nih.gov/pubmed/34505576 http://dx.doi.org/10.7554/eLife.64303 |
_version_ | 1783752551503495168 |
---|---|
author | Lemke, Stefan M Ramanathan, Dhakshin S Darevksy, David Egert, Daniel Berke, Joshua D Ganguly, Karunesh |
author_facet | Lemke, Stefan M Ramanathan, Dhakshin S Darevksy, David Egert, Daniel Berke, Joshua D Ganguly, Karunesh |
author_sort | Lemke, Stefan M |
collection | PubMed |
description | The strength of cortical connectivity to the striatum influences the balance between behavioral variability and stability. Learning to consistently produce a skilled action requires plasticity in corticostriatal connectivity associated with repeated training of the action. However, it remains unknown whether such corticostriatal plasticity occurs during training itself or ‘offline’ during time away from training, such as sleep. Here, we monitor the corticostriatal network throughout long-term skill learning in rats and find that non-rapid-eye-movement (NREM) sleep is a relevant period for corticostriatal plasticity. We first show that the offline activation of striatal NMDA receptors is required for skill learning. We then show that corticostriatal functional connectivity increases offline, coupled to emerging consistent skilled movements, and coupled cross-area neural dynamics. We then identify NREM sleep spindles as uniquely poised to mediate corticostriatal plasticity, through interactions with slow oscillations. Our results provide evidence that sleep shapes cross-area coupling required for skill learning. |
format | Online Article Text |
id | pubmed-8439654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-84396542021-09-15 Coupling between motor cortex and striatum increases during sleep over long-term skill learning Lemke, Stefan M Ramanathan, Dhakshin S Darevksy, David Egert, Daniel Berke, Joshua D Ganguly, Karunesh eLife Neuroscience The strength of cortical connectivity to the striatum influences the balance between behavioral variability and stability. Learning to consistently produce a skilled action requires plasticity in corticostriatal connectivity associated with repeated training of the action. However, it remains unknown whether such corticostriatal plasticity occurs during training itself or ‘offline’ during time away from training, such as sleep. Here, we monitor the corticostriatal network throughout long-term skill learning in rats and find that non-rapid-eye-movement (NREM) sleep is a relevant period for corticostriatal plasticity. We first show that the offline activation of striatal NMDA receptors is required for skill learning. We then show that corticostriatal functional connectivity increases offline, coupled to emerging consistent skilled movements, and coupled cross-area neural dynamics. We then identify NREM sleep spindles as uniquely poised to mediate corticostriatal plasticity, through interactions with slow oscillations. Our results provide evidence that sleep shapes cross-area coupling required for skill learning. eLife Sciences Publications, Ltd 2021-09-10 /pmc/articles/PMC8439654/ /pubmed/34505576 http://dx.doi.org/10.7554/eLife.64303 Text en © 2021, Lemke et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Lemke, Stefan M Ramanathan, Dhakshin S Darevksy, David Egert, Daniel Berke, Joshua D Ganguly, Karunesh Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title | Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title_full | Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title_fullStr | Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title_full_unstemmed | Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title_short | Coupling between motor cortex and striatum increases during sleep over long-term skill learning |
title_sort | coupling between motor cortex and striatum increases during sleep over long-term skill learning |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8439654/ https://www.ncbi.nlm.nih.gov/pubmed/34505576 http://dx.doi.org/10.7554/eLife.64303 |
work_keys_str_mv | AT lemkestefanm couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning AT ramanathandhakshins couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning AT darevksydavid couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning AT egertdaniel couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning AT berkejoshuad couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning AT gangulykarunesh couplingbetweenmotorcortexandstriatumincreasesduringsleepoverlongtermskilllearning |