Cargando…

Bidirectional propagation of low frequency oscillations over the human hippocampal surface

The hippocampus is diversely interconnected with other brain systems along its axis. Cycles of theta-frequency activity are believed to propagate from the septal to temporal pole, yet it is unclear how this one-way route supports the flexible cognitive capacities of this structure. We leveraged nove...

Descripción completa

Detalles Bibliográficos
Autores principales: Kleen, Jonathan K., Chung, Jason E., Sellers, Kristin K., Zhou, Jenny, Triplett, Michael, Lee, Kye, Tooker, Angela, Haque, Razi, Chang, Edward F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115072/
https://www.ncbi.nlm.nih.gov/pubmed/33980852
http://dx.doi.org/10.1038/s41467-021-22850-5
_version_ 1783691168856408064
author Kleen, Jonathan K.
Chung, Jason E.
Sellers, Kristin K.
Zhou, Jenny
Triplett, Michael
Lee, Kye
Tooker, Angela
Haque, Razi
Chang, Edward F.
author_facet Kleen, Jonathan K.
Chung, Jason E.
Sellers, Kristin K.
Zhou, Jenny
Triplett, Michael
Lee, Kye
Tooker, Angela
Haque, Razi
Chang, Edward F.
author_sort Kleen, Jonathan K.
collection PubMed
description The hippocampus is diversely interconnected with other brain systems along its axis. Cycles of theta-frequency activity are believed to propagate from the septal to temporal pole, yet it is unclear how this one-way route supports the flexible cognitive capacities of this structure. We leveraged novel thin-film microgrid arrays conformed to the human hippocampal surface to track neural activity two-dimensionally in vivo. All oscillation frequencies identified between 1–15 Hz propagated across the tissue. Moreover, they dynamically shifted between two roughly opposite directions oblique to the long axis. This predominant propagation axis was mirrored across participants, hemispheres, and consciousness states. Directionality was modulated in a participant who performed a behavioral task, and it could be predicted by wave amplitude topography over the hippocampal surface. Our results show that propagation directions may thus represent distinct meso-scale network computations, operating along versatile spatiotemporal processing routes across the hippocampal body.
format Online
Article
Text
id pubmed-8115072
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-81150722021-05-14 Bidirectional propagation of low frequency oscillations over the human hippocampal surface Kleen, Jonathan K. Chung, Jason E. Sellers, Kristin K. Zhou, Jenny Triplett, Michael Lee, Kye Tooker, Angela Haque, Razi Chang, Edward F. Nat Commun Article The hippocampus is diversely interconnected with other brain systems along its axis. Cycles of theta-frequency activity are believed to propagate from the septal to temporal pole, yet it is unclear how this one-way route supports the flexible cognitive capacities of this structure. We leveraged novel thin-film microgrid arrays conformed to the human hippocampal surface to track neural activity two-dimensionally in vivo. All oscillation frequencies identified between 1–15 Hz propagated across the tissue. Moreover, they dynamically shifted between two roughly opposite directions oblique to the long axis. This predominant propagation axis was mirrored across participants, hemispheres, and consciousness states. Directionality was modulated in a participant who performed a behavioral task, and it could be predicted by wave amplitude topography over the hippocampal surface. Our results show that propagation directions may thus represent distinct meso-scale network computations, operating along versatile spatiotemporal processing routes across the hippocampal body. Nature Publishing Group UK 2021-05-12 /pmc/articles/PMC8115072/ /pubmed/33980852 http://dx.doi.org/10.1038/s41467-021-22850-5 Text en © The Author(s) 2021 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
Kleen, Jonathan K.
Chung, Jason E.
Sellers, Kristin K.
Zhou, Jenny
Triplett, Michael
Lee, Kye
Tooker, Angela
Haque, Razi
Chang, Edward F.
Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title_full Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title_fullStr Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title_full_unstemmed Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title_short Bidirectional propagation of low frequency oscillations over the human hippocampal surface
title_sort bidirectional propagation of low frequency oscillations over the human hippocampal surface
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115072/
https://www.ncbi.nlm.nih.gov/pubmed/33980852
http://dx.doi.org/10.1038/s41467-021-22850-5
work_keys_str_mv AT kleenjonathank bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT chungjasone bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT sellerskristink bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT zhoujenny bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT triplettmichael bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT leekye bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT tookerangela bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT haquerazi bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface
AT changedwardf bidirectionalpropagationoflowfrequencyoscillationsoverthehumanhippocampalsurface