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Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks

The neurobiological basis of learning is reflected in adaptations of brain structure, network organization and energy metabolism. However, it is still unknown how different neuroplastic mechanisms act together and if cognitive advancements relate to general or task-specific changes. Therefore, we te...

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Autores principales: Klug, Sebastian, Godbersen, Godber M., Rischka, Lucas, Wadsak, Wolfgang, Pichler, Verena, Klöbl, Manfred, Hacker, Marcus, Lanzenberger, Rupert, Hahn, Andreas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085889/
https://www.ncbi.nlm.nih.gov/pubmed/35534605
http://dx.doi.org/10.1038/s42003-022-03362-4
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author Klug, Sebastian
Godbersen, Godber M.
Rischka, Lucas
Wadsak, Wolfgang
Pichler, Verena
Klöbl, Manfred
Hacker, Marcus
Lanzenberger, Rupert
Hahn, Andreas
author_facet Klug, Sebastian
Godbersen, Godber M.
Rischka, Lucas
Wadsak, Wolfgang
Pichler, Verena
Klöbl, Manfred
Hacker, Marcus
Lanzenberger, Rupert
Hahn, Andreas
author_sort Klug, Sebastian
collection PubMed
description The neurobiological basis of learning is reflected in adaptations of brain structure, network organization and energy metabolism. However, it is still unknown how different neuroplastic mechanisms act together and if cognitive advancements relate to general or task-specific changes. Therefore, we tested how hierarchical network interactions contribute to improvements in the performance of a visuo-spatial processing task by employing simultaneous PET/MR neuroimaging before and after a 4-week learning period. We combined functional PET and metabolic connectivity mapping (MCM) to infer directional interactions across brain regions. Learning altered the top-down regulation of the salience network onto the occipital cortex, with increases in MCM at resting-state and decreases during task execution. Accordingly, a higher divergence between resting-state and task-specific effects was associated with better cognitive performance, indicating that these adaptations are complementary and both required for successful visuo-spatial skill learning. Simulations further showed that changes at resting-state were dependent on glucose metabolism, whereas those during task performance were driven by functional connectivity between salience and visual networks. Referring to previous work, we suggest that learning establishes a metabolically expensive skill engram at rest, whose retrieval serves for efficient task execution by minimizing prediction errors between neuronal representations of brain regions on different hierarchical levels.
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spelling pubmed-90858892022-05-11 Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks Klug, Sebastian Godbersen, Godber M. Rischka, Lucas Wadsak, Wolfgang Pichler, Verena Klöbl, Manfred Hacker, Marcus Lanzenberger, Rupert Hahn, Andreas Commun Biol Article The neurobiological basis of learning is reflected in adaptations of brain structure, network organization and energy metabolism. However, it is still unknown how different neuroplastic mechanisms act together and if cognitive advancements relate to general or task-specific changes. Therefore, we tested how hierarchical network interactions contribute to improvements in the performance of a visuo-spatial processing task by employing simultaneous PET/MR neuroimaging before and after a 4-week learning period. We combined functional PET and metabolic connectivity mapping (MCM) to infer directional interactions across brain regions. Learning altered the top-down regulation of the salience network onto the occipital cortex, with increases in MCM at resting-state and decreases during task execution. Accordingly, a higher divergence between resting-state and task-specific effects was associated with better cognitive performance, indicating that these adaptations are complementary and both required for successful visuo-spatial skill learning. Simulations further showed that changes at resting-state were dependent on glucose metabolism, whereas those during task performance were driven by functional connectivity between salience and visual networks. Referring to previous work, we suggest that learning establishes a metabolically expensive skill engram at rest, whose retrieval serves for efficient task execution by minimizing prediction errors between neuronal representations of brain regions on different hierarchical levels. Nature Publishing Group UK 2022-05-09 /pmc/articles/PMC9085889/ /pubmed/35534605 http://dx.doi.org/10.1038/s42003-022-03362-4 Text en © The Author(s) 2022 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Klug, Sebastian
Godbersen, Godber M.
Rischka, Lucas
Wadsak, Wolfgang
Pichler, Verena
Klöbl, Manfred
Hacker, Marcus
Lanzenberger, Rupert
Hahn, Andreas
Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title_full Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title_fullStr Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title_full_unstemmed Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title_short Learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
title_sort learning induces coordinated neuronal plasticity of metabolic demands and functional brain networks
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9085889/
https://www.ncbi.nlm.nih.gov/pubmed/35534605
http://dx.doi.org/10.1038/s42003-022-03362-4
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