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Sampling motion trajectories during hippocampal theta sequences

Efficient planning in complex environments requires that uncertainty associated with current inferences and possible consequences of forthcoming actions is represented. Representation of uncertainty has been established in sensory systems during simple perceptual decision making tasks but it remains...

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Detalles Bibliográficos
Autores principales: Ujfalussy, Balazs B, Orbán, Gergő
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643003/
https://www.ncbi.nlm.nih.gov/pubmed/36346218
http://dx.doi.org/10.7554/eLife.74058
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author Ujfalussy, Balazs B
Orbán, Gergő
author_facet Ujfalussy, Balazs B
Orbán, Gergő
author_sort Ujfalussy, Balazs B
collection PubMed
description Efficient planning in complex environments requires that uncertainty associated with current inferences and possible consequences of forthcoming actions is represented. Representation of uncertainty has been established in sensory systems during simple perceptual decision making tasks but it remains unclear if complex cognitive computations such as planning and navigation are also supported by probabilistic neural representations. Here, we capitalized on gradually changing uncertainty along planned motion trajectories during hippocampal theta sequences to capture signatures of uncertainty representation in population responses. In contrast with prominent theories, we found no evidence of encoding parameters of probability distributions in the momentary population activity recorded in an open-field navigation task in rats. Instead, uncertainty was encoded sequentially by sampling motion trajectories randomly and efficiently in subsequent theta cycles from the distribution of potential trajectories. Our analysis is the first to demonstrate that the hippocampus is well equipped to contribute to optimal planning by representing uncertainty.
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spelling pubmed-96430032022-11-15 Sampling motion trajectories during hippocampal theta sequences Ujfalussy, Balazs B Orbán, Gergő eLife Neuroscience Efficient planning in complex environments requires that uncertainty associated with current inferences and possible consequences of forthcoming actions is represented. Representation of uncertainty has been established in sensory systems during simple perceptual decision making tasks but it remains unclear if complex cognitive computations such as planning and navigation are also supported by probabilistic neural representations. Here, we capitalized on gradually changing uncertainty along planned motion trajectories during hippocampal theta sequences to capture signatures of uncertainty representation in population responses. In contrast with prominent theories, we found no evidence of encoding parameters of probability distributions in the momentary population activity recorded in an open-field navigation task in rats. Instead, uncertainty was encoded sequentially by sampling motion trajectories randomly and efficiently in subsequent theta cycles from the distribution of potential trajectories. Our analysis is the first to demonstrate that the hippocampus is well equipped to contribute to optimal planning by representing uncertainty. eLife Sciences Publications, Ltd 2022-11-08 /pmc/articles/PMC9643003/ /pubmed/36346218 http://dx.doi.org/10.7554/eLife.74058 Text en © 2022, Ujfalussy and Orbán 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
Ujfalussy, Balazs B
Orbán, Gergő
Sampling motion trajectories during hippocampal theta sequences
title Sampling motion trajectories during hippocampal theta sequences
title_full Sampling motion trajectories during hippocampal theta sequences
title_fullStr Sampling motion trajectories during hippocampal theta sequences
title_full_unstemmed Sampling motion trajectories during hippocampal theta sequences
title_short Sampling motion trajectories during hippocampal theta sequences
title_sort sampling motion trajectories during hippocampal theta sequences
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643003/
https://www.ncbi.nlm.nih.gov/pubmed/36346218
http://dx.doi.org/10.7554/eLife.74058
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