Asymmetry of the temporal code for space by hippocampal place cells
Abstract 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 t...
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Nature Portfolio
2017
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oai:doaj.org-article:96f7696c70f34aa2ba418a46bd4d97e02021-12-02T12:32:45ZAsymmetry of the temporal code for space by hippocampal place cells10.1038/s41598-017-08609-32045-2322https://doaj.org/article/96f7696c70f34aa2ba418a46bd4d97e02017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-08609-3https://doaj.org/toc/2045-2322Abstract 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.Bryan C. SouzaAdriano B. L. TortNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-9 (2017) |
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Medicine R Science Q Bryan C. Souza Adriano B. L. Tort Asymmetry of the temporal code for space by hippocampal place cells |
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Abstract 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. |
format |
article |
author |
Bryan C. Souza Adriano B. L. Tort |
author_facet |
Bryan C. Souza Adriano B. L. Tort |
author_sort |
Bryan C. Souza |
title |
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_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_sort |
asymmetry of the temporal code for space by hippocampal place cells |
publisher |
Nature Portfolio |
publishDate |
2017 |
url |
https://doaj.org/article/96f7696c70f34aa2ba418a46bd4d97e0 |
work_keys_str_mv |
AT bryancsouza asymmetryofthetemporalcodeforspacebyhippocampalplacecells AT adrianobltort asymmetryofthetemporalcodeforspacebyhippocampalplacecells |
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1718393993122807808 |