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Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate
Spiking activity of place cells in the hippocampus encodes the animal’s position as it moves through an environment. Within a cell’s place field, both the firing rate and the phase of spiking in the local theta oscillation contain spatial information. We propose a position–theta-phase (PTP) model th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936353/ https://www.ncbi.nlm.nih.gov/pubmed/31843934 http://dx.doi.org/10.1073/pnas.1912792116 |
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author | McClain, Kathryn Tingley, David Heeger, David J. Buzsáki, György |
author_facet | McClain, Kathryn Tingley, David Heeger, David J. Buzsáki, György |
author_sort | McClain, Kathryn |
collection | PubMed |
description | Spiking activity of place cells in the hippocampus encodes the animal’s position as it moves through an environment. Within a cell’s place field, both the firing rate and the phase of spiking in the local theta oscillation contain spatial information. We propose a position–theta-phase (PTP) model that captures the simultaneous expression of the firing-rate code and theta-phase code in place cell spiking. This model parametrically characterizes place fields to compare across cells, time, and conditions; generates realistic place cell simulation data; and conceptualizes a framework for principled hypothesis testing to identify additional features of place cell activity. We use the PTP model to assess the effect of running speed in place cell data recorded from rats running on linear tracks. For the majority of place fields, we do not find evidence for speed modulation of the firing rate. For a small subset of place fields, we find firing rates significantly increase or decrease with speed. We use the PTP model to compare candidate mechanisms of speed modulation in significantly modulated fields and determine that speed acts as a gain control on the magnitude of firing rate. Our model provides a tool that connects rigorous analysis with a computational framework for understanding place cell activity. |
format | Online Article Text |
id | pubmed-6936353 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-69363532019-12-31 Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate McClain, Kathryn Tingley, David Heeger, David J. Buzsáki, György Proc Natl Acad Sci U S A Biological Sciences Spiking activity of place cells in the hippocampus encodes the animal’s position as it moves through an environment. Within a cell’s place field, both the firing rate and the phase of spiking in the local theta oscillation contain spatial information. We propose a position–theta-phase (PTP) model that captures the simultaneous expression of the firing-rate code and theta-phase code in place cell spiking. This model parametrically characterizes place fields to compare across cells, time, and conditions; generates realistic place cell simulation data; and conceptualizes a framework for principled hypothesis testing to identify additional features of place cell activity. We use the PTP model to assess the effect of running speed in place cell data recorded from rats running on linear tracks. For the majority of place fields, we do not find evidence for speed modulation of the firing rate. For a small subset of place fields, we find firing rates significantly increase or decrease with speed. We use the PTP model to compare candidate mechanisms of speed modulation in significantly modulated fields and determine that speed acts as a gain control on the magnitude of firing rate. Our model provides a tool that connects rigorous analysis with a computational framework for understanding place cell activity. National Academy of Sciences 2019-12-26 2019-12-16 /pmc/articles/PMC6936353/ /pubmed/31843934 http://dx.doi.org/10.1073/pnas.1912792116 Text en Copyright © 2019 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences McClain, Kathryn Tingley, David Heeger, David J. Buzsáki, György Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title | Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title_full | Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title_fullStr | Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title_full_unstemmed | Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title_short | Position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
title_sort | position–theta-phase model of hippocampal place cell activity applied to quantification of running speed modulation of firing rate |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6936353/ https://www.ncbi.nlm.nih.gov/pubmed/31843934 http://dx.doi.org/10.1073/pnas.1912792116 |
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