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Asymmetry of the temporal code for space by hippocampal place cells

Hippocampal place cells convey spatial information through spike frequency (“rate coding”) and spike timing relative to the theta phase (“temporal coding”). Whether rate and temporal coding are due to independent or related mechanisms has been the subject of wide debate. Here we show that the spike...

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Detalles Bibliográficos
Autores principales: Souza, Bryan C., Tort, Adriano B. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561149/
https://www.ncbi.nlm.nih.gov/pubmed/28819301
http://dx.doi.org/10.1038/s41598-017-08609-3
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author Souza, Bryan C.
Tort, Adriano B. L.
author_facet Souza, Bryan C.
Tort, Adriano B. L.
author_sort Souza, Bryan C.
collection PubMed
description Hippocampal place cells convey spatial information through spike frequency (“rate coding”) and spike timing relative to the theta phase (“temporal coding”). Whether rate and temporal coding are due to independent or related mechanisms has been the subject of wide debate. Here we show that the spike timing of place cells couples to theta phase before major increases in firing rate, anticipating the animal’s entrance into the classical, rate-based place field. In contrast, spikes rapidly decouple from theta as the animal leaves the place field and firing rate decreases. Therefore, temporal coding has strong asymmetry around the place field center. We further show that the dynamics of temporal coding along space evolves in three stages as the animal traverses the place field: phase coupling, sharp precession and phase decoupling. These results suggest that independent mechanisms may govern rate and temporal coding.
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spelling pubmed-55611492017-08-18 Asymmetry of the temporal code for space by hippocampal place cells Souza, Bryan C. Tort, Adriano B. L. Sci Rep Article Hippocampal place cells convey spatial information through spike frequency (“rate coding”) and spike timing relative to the theta phase (“temporal coding”). Whether rate and temporal coding are due to independent or related mechanisms has been the subject of wide debate. Here we show that the spike timing of place cells couples to theta phase before major increases in firing rate, anticipating the animal’s entrance into the classical, rate-based place field. In contrast, spikes rapidly decouple from theta as the animal leaves the place field and firing rate decreases. Therefore, temporal coding has strong asymmetry around the place field center. We further show that the dynamics of temporal coding along space evolves in three stages as the animal traverses the place field: phase coupling, sharp precession and phase decoupling. These results suggest that independent mechanisms may govern rate and temporal coding. Nature Publishing Group UK 2017-08-17 /pmc/articles/PMC5561149/ /pubmed/28819301 http://dx.doi.org/10.1038/s41598-017-08609-3 Text en © The Author(s) 2017 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/.
spellingShingle Article
Souza, Bryan C.
Tort, Adriano B. L.
Asymmetry of the temporal code for space by hippocampal place cells
title Asymmetry of the temporal code for space by hippocampal place cells
title_full Asymmetry of the temporal code for space by hippocampal place cells
title_fullStr Asymmetry of the temporal code for space by hippocampal place cells
title_full_unstemmed Asymmetry of the temporal code for space by hippocampal place cells
title_short Asymmetry of the temporal code for space by hippocampal place cells
title_sort asymmetry of the temporal code for space by hippocampal place cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5561149/
https://www.ncbi.nlm.nih.gov/pubmed/28819301
http://dx.doi.org/10.1038/s41598-017-08609-3
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