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Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task
We introduce a computational model describing rat behavior and the interactions of neural populations processing spatial and mnemonic information during a maze-based, decision-making task. The model integrates sensory input and implements working memory to inform decisions at a choice point, reprodu...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939443/ https://www.ncbi.nlm.nih.gov/pubmed/24624066 http://dx.doi.org/10.3389/fnbeh.2014.00062 |
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author | Jahans-Price, Thomas Gorochowski, Thomas E. Wilson, Matthew A. Jones, Matthew W. Bogacz, Rafal |
author_facet | Jahans-Price, Thomas Gorochowski, Thomas E. Wilson, Matthew A. Jones, Matthew W. Bogacz, Rafal |
author_sort | Jahans-Price, Thomas |
collection | PubMed |
description | We introduce a computational model describing rat behavior and the interactions of neural populations processing spatial and mnemonic information during a maze-based, decision-making task. The model integrates sensory input and implements working memory to inform decisions at a choice point, reproducing rat behavioral data and predicting the occurrence of turn- and memory-dependent activity in neuronal networks subserving task performance. We tested these model predictions using a new software toolbox (Maze Query Language, MQL) to analyse activity of medial prefrontal cortical (mPFC) and dorsal hippocampal (dCA1) neurons recorded from six adult rats during task performance. The firing rates of dCA1 neurons discriminated context (i.e., the direction of the previous turn), whilst a subset of mPFC neurons was selective for current turn direction or context, with some conjunctively encoding both. mPFC turn-selective neurons displayed a ramping of activity on approach to the decision turn and turn-selectivity in mPFC was significantly reduced during error trials. These analyses complement data from neurophysiological recordings in non-human primates indicating that firing rates of cortical neurons correlate with integration of sensory evidence used to inform decision-making. |
format | Online Article Text |
id | pubmed-3939443 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-39394432014-03-12 Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task Jahans-Price, Thomas Gorochowski, Thomas E. Wilson, Matthew A. Jones, Matthew W. Bogacz, Rafal Front Behav Neurosci Neuroscience We introduce a computational model describing rat behavior and the interactions of neural populations processing spatial and mnemonic information during a maze-based, decision-making task. The model integrates sensory input and implements working memory to inform decisions at a choice point, reproducing rat behavioral data and predicting the occurrence of turn- and memory-dependent activity in neuronal networks subserving task performance. We tested these model predictions using a new software toolbox (Maze Query Language, MQL) to analyse activity of medial prefrontal cortical (mPFC) and dorsal hippocampal (dCA1) neurons recorded from six adult rats during task performance. The firing rates of dCA1 neurons discriminated context (i.e., the direction of the previous turn), whilst a subset of mPFC neurons was selective for current turn direction or context, with some conjunctively encoding both. mPFC turn-selective neurons displayed a ramping of activity on approach to the decision turn and turn-selectivity in mPFC was significantly reduced during error trials. These analyses complement data from neurophysiological recordings in non-human primates indicating that firing rates of cortical neurons correlate with integration of sensory evidence used to inform decision-making. Frontiers Media S.A. 2014-03-03 /pmc/articles/PMC3939443/ /pubmed/24624066 http://dx.doi.org/10.3389/fnbeh.2014.00062 Text en Copyright © 2014 Jahans-Price, Gorochowski, Wilson, Jones and Bogacz. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Jahans-Price, Thomas Gorochowski, Thomas E. Wilson, Matthew A. Jones, Matthew W. Bogacz, Rafal Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title | Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title_full | Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title_fullStr | Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title_full_unstemmed | Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title_short | Computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
title_sort | computational modeling and analysis of hippocampal-prefrontal information coding during a spatial decision-making task |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3939443/ https://www.ncbi.nlm.nih.gov/pubmed/24624066 http://dx.doi.org/10.3389/fnbeh.2014.00062 |
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