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Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain

BACKGROUND: In mammals, the slow-oscillations of neuronal membrane potentials (reflected in the electroencephalogram as high-amplitude, slow-waves), which occur during non-rapid eye movement sleep and anesthesia, propagate across the neocortex largely as two-dimensional traveling waves. However, it...

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Autores principales: Beckers, Gabriël JL, van der Meij, Jacqueline, Lesku, John A, Rattenborg, Niels C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015294/
https://www.ncbi.nlm.nih.gov/pubmed/24580797
http://dx.doi.org/10.1186/1741-7007-12-16
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author Beckers, Gabriël JL
van der Meij, Jacqueline
Lesku, John A
Rattenborg, Niels C
author_facet Beckers, Gabriël JL
van der Meij, Jacqueline
Lesku, John A
Rattenborg, Niels C
author_sort Beckers, Gabriël JL
collection PubMed
description BACKGROUND: In mammals, the slow-oscillations of neuronal membrane potentials (reflected in the electroencephalogram as high-amplitude, slow-waves), which occur during non-rapid eye movement sleep and anesthesia, propagate across the neocortex largely as two-dimensional traveling waves. However, it remains unknown if the traveling nature of slow-waves is unique to the laminar cytoarchitecture and associated computational properties of the neocortex. RESULTS: We demonstrate that local field potential slow-waves and correlated multiunit activity propagate as complex three-dimensional plumes of neuronal activity through the avian brain, owing to its non-laminar, nuclear neuronal cytoarchitecture. CONCLUSIONS: The traveling nature of slow-waves is not dependent upon the laminar organization of the neocortex, and is unlikely to subserve functions unique to this pattern of neuronal organization. Finally, the three-dimensional geometry of propagating plumes may reflect computational properties not found in mammals that contributed to the evolution of nuclear neuronal organization and complex cognition in birds.
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spelling pubmed-40152942014-05-10 Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain Beckers, Gabriël JL van der Meij, Jacqueline Lesku, John A Rattenborg, Niels C BMC Biol Research Article BACKGROUND: In mammals, the slow-oscillations of neuronal membrane potentials (reflected in the electroencephalogram as high-amplitude, slow-waves), which occur during non-rapid eye movement sleep and anesthesia, propagate across the neocortex largely as two-dimensional traveling waves. However, it remains unknown if the traveling nature of slow-waves is unique to the laminar cytoarchitecture and associated computational properties of the neocortex. RESULTS: We demonstrate that local field potential slow-waves and correlated multiunit activity propagate as complex three-dimensional plumes of neuronal activity through the avian brain, owing to its non-laminar, nuclear neuronal cytoarchitecture. CONCLUSIONS: The traveling nature of slow-waves is not dependent upon the laminar organization of the neocortex, and is unlikely to subserve functions unique to this pattern of neuronal organization. Finally, the three-dimensional geometry of propagating plumes may reflect computational properties not found in mammals that contributed to the evolution of nuclear neuronal organization and complex cognition in birds. BioMed Central 2014-02-28 /pmc/articles/PMC4015294/ /pubmed/24580797 http://dx.doi.org/10.1186/1741-7007-12-16 Text en Copyright © 2014 Beckers et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Beckers, Gabriël JL
van der Meij, Jacqueline
Lesku, John A
Rattenborg, Niels C
Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title_full Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title_fullStr Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title_full_unstemmed Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title_short Plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
title_sort plumes of neuronal activity propagate in three dimensions through the nuclear avian brain
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4015294/
https://www.ncbi.nlm.nih.gov/pubmed/24580797
http://dx.doi.org/10.1186/1741-7007-12-16
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