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Lamina-specific cortical dynamics in human visual and sensorimotor cortices
Distinct anatomical and spectral channels are thought to play specialized roles in the communication within cortical networks. While activity in the alpha and beta frequency range (7 – 40 Hz) is thought to predominantly originate from infragranular cortical layers conveying feedback-related informat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197856/ https://www.ncbi.nlm.nih.gov/pubmed/30346274 http://dx.doi.org/10.7554/eLife.33977 |
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author | Bonaiuto, James J Meyer, Sofie S Little, Simon Rossiter, Holly Callaghan, Martina F Dick, Frederic Barnes, Gareth R Bestmann, Sven |
author_facet | Bonaiuto, James J Meyer, Sofie S Little, Simon Rossiter, Holly Callaghan, Martina F Dick, Frederic Barnes, Gareth R Bestmann, Sven |
author_sort | Bonaiuto, James J |
collection | PubMed |
description | Distinct anatomical and spectral channels are thought to play specialized roles in the communication within cortical networks. While activity in the alpha and beta frequency range (7 – 40 Hz) is thought to predominantly originate from infragranular cortical layers conveying feedback-related information, activity in the gamma range (>40 Hz) dominates in supragranular layers communicating feedforward signals. We leveraged high precision MEG to test this proposal, directly and non-invasively, in human participants performing visually cued actions. We found that visual alpha mapped onto deep cortical laminae, whereas visual gamma predominantly occurred more superficially. This lamina-specificity was echoed in movement-related sensorimotor beta and gamma activity. These lamina-specific pre- and post- movement changes in sensorimotor beta and gamma activity suggest a more complex functional role than the proposed feedback and feedforward communication in sensory cortex. Distinct frequency channels thus operate in a lamina-specific manner across cortex, but may fulfill distinct functional roles in sensory and motor processes. |
format | Online Article Text |
id | pubmed-6197856 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-61978562018-10-24 Lamina-specific cortical dynamics in human visual and sensorimotor cortices Bonaiuto, James J Meyer, Sofie S Little, Simon Rossiter, Holly Callaghan, Martina F Dick, Frederic Barnes, Gareth R Bestmann, Sven eLife Neuroscience Distinct anatomical and spectral channels are thought to play specialized roles in the communication within cortical networks. While activity in the alpha and beta frequency range (7 – 40 Hz) is thought to predominantly originate from infragranular cortical layers conveying feedback-related information, activity in the gamma range (>40 Hz) dominates in supragranular layers communicating feedforward signals. We leveraged high precision MEG to test this proposal, directly and non-invasively, in human participants performing visually cued actions. We found that visual alpha mapped onto deep cortical laminae, whereas visual gamma predominantly occurred more superficially. This lamina-specificity was echoed in movement-related sensorimotor beta and gamma activity. These lamina-specific pre- and post- movement changes in sensorimotor beta and gamma activity suggest a more complex functional role than the proposed feedback and feedforward communication in sensory cortex. Distinct frequency channels thus operate in a lamina-specific manner across cortex, but may fulfill distinct functional roles in sensory and motor processes. eLife Sciences Publications, Ltd 2018-10-22 /pmc/articles/PMC6197856/ /pubmed/30346274 http://dx.doi.org/10.7554/eLife.33977 Text en © 2018, Bonaiuto et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Bonaiuto, James J Meyer, Sofie S Little, Simon Rossiter, Holly Callaghan, Martina F Dick, Frederic Barnes, Gareth R Bestmann, Sven Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title | Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title_full | Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title_fullStr | Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title_full_unstemmed | Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title_short | Lamina-specific cortical dynamics in human visual and sensorimotor cortices |
title_sort | lamina-specific cortical dynamics in human visual and sensorimotor cortices |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6197856/ https://www.ncbi.nlm.nih.gov/pubmed/30346274 http://dx.doi.org/10.7554/eLife.33977 |
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