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Internally generated time in the rodent hippocampus is logarithmically compressed

The Weber-Fechner law proposes that our perceived sensory input increases with physical input on a logarithmic scale. Hippocampal ‘time cells’ carry a record of recent experience by firing sequentially during a circumscribed period of time after a triggering stimulus. Different cells have ‘time fiel...

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Autores principales: Cao, Rui, Bladon, John H, Charczynski, Stephen J, Hasselmo, Michael E, Howard, Marc W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651951/
https://www.ncbi.nlm.nih.gov/pubmed/36250631
http://dx.doi.org/10.7554/eLife.75353
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author Cao, Rui
Bladon, John H
Charczynski, Stephen J
Hasselmo, Michael E
Howard, Marc W
author_facet Cao, Rui
Bladon, John H
Charczynski, Stephen J
Hasselmo, Michael E
Howard, Marc W
author_sort Cao, Rui
collection PubMed
description The Weber-Fechner law proposes that our perceived sensory input increases with physical input on a logarithmic scale. Hippocampal ‘time cells’ carry a record of recent experience by firing sequentially during a circumscribed period of time after a triggering stimulus. Different cells have ‘time fields’ at different delays up to at least tens of seconds. Past studies suggest that time cells represent a compressed timeline by demonstrating that fewer time cells fire late in the delay and their time fields are wider. This paper asks whether the compression of time cells obeys the Weber-Fechner Law. Time cells were studied with a hierarchical Bayesian model that simultaneously accounts for the firing pattern at the trial level, cell level, and population level. This procedure allows separate estimates of the within-trial receptive field width and the across-trial variability. After isolating across-trial variability, time field width increased linearly with delay. Further, the time cell population was distributed evenly along a logarithmic time axis. These findings provide strong quantitative evidence that the neural temporal representation in rodent hippocampus is logarithmically compressed and obeys a neural Weber-Fechner Law.
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spelling pubmed-96519512022-11-15 Internally generated time in the rodent hippocampus is logarithmically compressed Cao, Rui Bladon, John H Charczynski, Stephen J Hasselmo, Michael E Howard, Marc W eLife Neuroscience The Weber-Fechner law proposes that our perceived sensory input increases with physical input on a logarithmic scale. Hippocampal ‘time cells’ carry a record of recent experience by firing sequentially during a circumscribed period of time after a triggering stimulus. Different cells have ‘time fields’ at different delays up to at least tens of seconds. Past studies suggest that time cells represent a compressed timeline by demonstrating that fewer time cells fire late in the delay and their time fields are wider. This paper asks whether the compression of time cells obeys the Weber-Fechner Law. Time cells were studied with a hierarchical Bayesian model that simultaneously accounts for the firing pattern at the trial level, cell level, and population level. This procedure allows separate estimates of the within-trial receptive field width and the across-trial variability. After isolating across-trial variability, time field width increased linearly with delay. Further, the time cell population was distributed evenly along a logarithmic time axis. These findings provide strong quantitative evidence that the neural temporal representation in rodent hippocampus is logarithmically compressed and obeys a neural Weber-Fechner Law. eLife Sciences Publications, Ltd 2022-10-17 /pmc/articles/PMC9651951/ /pubmed/36250631 http://dx.doi.org/10.7554/eLife.75353 Text en © 2022, Cao, Bladon et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Cao, Rui
Bladon, John H
Charczynski, Stephen J
Hasselmo, Michael E
Howard, Marc W
Internally generated time in the rodent hippocampus is logarithmically compressed
title Internally generated time in the rodent hippocampus is logarithmically compressed
title_full Internally generated time in the rodent hippocampus is logarithmically compressed
title_fullStr Internally generated time in the rodent hippocampus is logarithmically compressed
title_full_unstemmed Internally generated time in the rodent hippocampus is logarithmically compressed
title_short Internally generated time in the rodent hippocampus is logarithmically compressed
title_sort internally generated time in the rodent hippocampus is logarithmically compressed
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9651951/
https://www.ncbi.nlm.nih.gov/pubmed/36250631
http://dx.doi.org/10.7554/eLife.75353
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