Subpopulations of neurons in lOFC encode previous and current rewards at time of choice

Studies of neural dynamics in lateral orbitofrontal cortex (lOFC) have shown that subsets of neurons that encode distinct aspects of behavior, such as value, may project to common downstream targets. However, it is unclear whether reward history, which may subserve lOFC’s well-documented role in lea...

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Autores principales: David L Hocker, Carlos D Brody, Cristina Savin, Christine M Constantinople
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Publicado: eLife Sciences Publications Ltd 2021
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Acceso en línea:https://doaj.org/article/b1fd5776733d4c0286576c239586eb0e
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spelling oai:doaj.org-article:b1fd5776733d4c0286576c239586eb0e2021-11-25T09:13:59ZSubpopulations of neurons in lOFC encode previous and current rewards at time of choice10.7554/eLife.701292050-084Xe70129https://doaj.org/article/b1fd5776733d4c0286576c239586eb0e2021-10-01T00:00:00Zhttps://elifesciences.org/articles/70129https://doaj.org/toc/2050-084XStudies of neural dynamics in lateral orbitofrontal cortex (lOFC) have shown that subsets of neurons that encode distinct aspects of behavior, such as value, may project to common downstream targets. However, it is unclear whether reward history, which may subserve lOFC’s well-documented role in learning, is represented by functional subpopulations in lOFC. Previously, we analyzed neural recordings from rats performing a value-based decision-making task, and we documented trial-by-trial learning that required lOFC (Constantinople et al., 2019). Here, we characterize functional subpopulations of lOFC neurons during behavior, including their encoding of task variables. We found five distinct clusters of lOFC neurons, either based on clustering of their trial-averaged peristimulus time histograms (PSTHs), or a feature space defined by their average conditional firing rates aligned to different task variables. We observed weak encoding of reward attributes, but stronger encoding of reward history, the animal’s left or right choice, and reward receipt across all clusters. Only one cluster, however, encoded the animal’s reward history at the time shortly preceding the choice, suggesting a possible role in integrating previous and current trial outcomes at the time of choice. This cluster also exhibits qualitatively similar responses to identified corticostriatal projection neurons in a recent study (Hirokawa et al., 2019), and suggests a possible role for subpopulations of lOFC neurons in mediating trial-by-trial learning.David L HockerCarlos D BrodyCristina SavinChristine M ConstantinopleeLife Sciences Publications Ltdarticleorbitofrontal cortexdecision-makingsequential biasclusteringgeneralized linear modellearningMedicineRScienceQBiology (General)QH301-705.5ENeLife, Vol 10 (2021)
institution DOAJ
collection DOAJ
language EN
topic orbitofrontal cortex
decision-making
sequential bias
clustering
generalized linear model
learning
Medicine
R
Science
Q
Biology (General)
QH301-705.5
spellingShingle orbitofrontal cortex
decision-making
sequential bias
clustering
generalized linear model
learning
Medicine
R
Science
Q
Biology (General)
QH301-705.5
David L Hocker
Carlos D Brody
Cristina Savin
Christine M Constantinople
Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
description Studies of neural dynamics in lateral orbitofrontal cortex (lOFC) have shown that subsets of neurons that encode distinct aspects of behavior, such as value, may project to common downstream targets. However, it is unclear whether reward history, which may subserve lOFC’s well-documented role in learning, is represented by functional subpopulations in lOFC. Previously, we analyzed neural recordings from rats performing a value-based decision-making task, and we documented trial-by-trial learning that required lOFC (Constantinople et al., 2019). Here, we characterize functional subpopulations of lOFC neurons during behavior, including their encoding of task variables. We found five distinct clusters of lOFC neurons, either based on clustering of their trial-averaged peristimulus time histograms (PSTHs), or a feature space defined by their average conditional firing rates aligned to different task variables. We observed weak encoding of reward attributes, but stronger encoding of reward history, the animal’s left or right choice, and reward receipt across all clusters. Only one cluster, however, encoded the animal’s reward history at the time shortly preceding the choice, suggesting a possible role in integrating previous and current trial outcomes at the time of choice. This cluster also exhibits qualitatively similar responses to identified corticostriatal projection neurons in a recent study (Hirokawa et al., 2019), and suggests a possible role for subpopulations of lOFC neurons in mediating trial-by-trial learning.
format article
author David L Hocker
Carlos D Brody
Cristina Savin
Christine M Constantinople
author_facet David L Hocker
Carlos D Brody
Cristina Savin
Christine M Constantinople
author_sort David L Hocker
title Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
title_short Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
title_full Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
title_fullStr Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
title_full_unstemmed Subpopulations of neurons in lOFC encode previous and current rewards at time of choice
title_sort subpopulations of neurons in lofc encode previous and current rewards at time of choice
publisher eLife Sciences Publications Ltd
publishDate 2021
url https://doaj.org/article/b1fd5776733d4c0286576c239586eb0e
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AT carlosdbrody subpopulationsofneuronsinlofcencodepreviousandcurrentrewardsattimeofchoice
AT cristinasavin subpopulationsofneuronsinlofcencodepreviousandcurrentrewardsattimeofchoice
AT christinemconstantinople subpopulationsofneuronsinlofcencodepreviousandcurrentrewardsattimeofchoice
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