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Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making

Experience and training are known to boost our skills and mold the brain’s organization and function. Yet, structural plasticity and functional neurotransmission are typically studied at different scales (large-scale networks, local circuits), limiting our understanding of the adaptive interactions...

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Autores principales: Ziminski, Joseph J., Frangou, Polytimi, Karlaftis, Vasilis M., Emir, Uzay, Kourtzi, Zoe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032544/
https://www.ncbi.nlm.nih.gov/pubmed/36897881
http://dx.doi.org/10.1371/journal.pbio.3002029
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author Ziminski, Joseph J.
Frangou, Polytimi
Karlaftis, Vasilis M.
Emir, Uzay
Kourtzi, Zoe
author_facet Ziminski, Joseph J.
Frangou, Polytimi
Karlaftis, Vasilis M.
Emir, Uzay
Kourtzi, Zoe
author_sort Ziminski, Joseph J.
collection PubMed
description Experience and training are known to boost our skills and mold the brain’s organization and function. Yet, structural plasticity and functional neurotransmission are typically studied at different scales (large-scale networks, local circuits), limiting our understanding of the adaptive interactions that support learning of complex cognitive skills in the adult brain. Here, we employ multimodal brain imaging to investigate the link between microstructural (myelination) and neurochemical (GABAergic) plasticity for decision-making. We test (in males, due to potential confounding menstrual cycle effects on GABA measurements in females) for changes in MRI-measured myelin, GABA, and functional connectivity before versus after training on a perceptual decision task that involves identifying targets in clutter. We demonstrate that training alters subcortical (pulvinar, hippocampus) myelination and its functional connectivity to visual cortex and relates to decreased visual cortex GABAergic inhibition. Modeling interactions between MRI measures of myelin, GABA, and functional connectivity indicates that pulvinar myelin plasticity interacts—through thalamocortical connectivity—with GABAergic inhibition in visual cortex to support learning. Our findings propose a dynamic interplay of adaptive microstructural and neurochemical plasticity in subcortico-cortical circuits that supports learning for optimized decision-making in the adult human brain.
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spelling pubmed-100325442023-03-23 Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making Ziminski, Joseph J. Frangou, Polytimi Karlaftis, Vasilis M. Emir, Uzay Kourtzi, Zoe PLoS Biol Research Article Experience and training are known to boost our skills and mold the brain’s organization and function. Yet, structural plasticity and functional neurotransmission are typically studied at different scales (large-scale networks, local circuits), limiting our understanding of the adaptive interactions that support learning of complex cognitive skills in the adult brain. Here, we employ multimodal brain imaging to investigate the link between microstructural (myelination) and neurochemical (GABAergic) plasticity for decision-making. We test (in males, due to potential confounding menstrual cycle effects on GABA measurements in females) for changes in MRI-measured myelin, GABA, and functional connectivity before versus after training on a perceptual decision task that involves identifying targets in clutter. We demonstrate that training alters subcortical (pulvinar, hippocampus) myelination and its functional connectivity to visual cortex and relates to decreased visual cortex GABAergic inhibition. Modeling interactions between MRI measures of myelin, GABA, and functional connectivity indicates that pulvinar myelin plasticity interacts—through thalamocortical connectivity—with GABAergic inhibition in visual cortex to support learning. Our findings propose a dynamic interplay of adaptive microstructural and neurochemical plasticity in subcortico-cortical circuits that supports learning for optimized decision-making in the adult human brain. Public Library of Science 2023-03-10 /pmc/articles/PMC10032544/ /pubmed/36897881 http://dx.doi.org/10.1371/journal.pbio.3002029 Text en © 2023 Ziminski et al 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 author and source are credited.
spellingShingle Research Article
Ziminski, Joseph J.
Frangou, Polytimi
Karlaftis, Vasilis M.
Emir, Uzay
Kourtzi, Zoe
Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title_full Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title_fullStr Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title_full_unstemmed Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title_short Microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
title_sort microstructural and neurochemical plasticity mechanisms interact to enhance human perceptual decision-making
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032544/
https://www.ncbi.nlm.nih.gov/pubmed/36897881
http://dx.doi.org/10.1371/journal.pbio.3002029
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