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Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation
Learning to predict rewards based on environmental cues is essential for survival. The orbitofrontal cortex (OFC) contributes to such learning, by conveying reward-related information to brain areas such as the ventral tegmental area (VTA). Despite this, how cue-reward memory representations form in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002110/ https://www.ncbi.nlm.nih.gov/pubmed/31160741 http://dx.doi.org/10.1038/s41593-019-0408-1 |
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author | Namboodiri, Vijay Mohan K. Otis, James M. van Heeswijk, Kay Voets, Elisa S. Alghorazi, Rizk A. Rodriguez-Romaguera, Jose Mihalas, Stefan Stuber, Garret D. |
author_facet | Namboodiri, Vijay Mohan K. Otis, James M. van Heeswijk, Kay Voets, Elisa S. Alghorazi, Rizk A. Rodriguez-Romaguera, Jose Mihalas, Stefan Stuber, Garret D. |
author_sort | Namboodiri, Vijay Mohan K. |
collection | PubMed |
description | Learning to predict rewards based on environmental cues is essential for survival. The orbitofrontal cortex (OFC) contributes to such learning, by conveying reward-related information to brain areas such as the ventral tegmental area (VTA). Despite this, how cue-reward memory representations form in individual OFC neurons and are modified based on new information is unknown. To address this, using in vivo 2-photon calcium imaging in mice, we tracked the response evolution of thousands of OFC output neurons, including those projecting to VTA, through multiple days and stages of cue-reward learning. Collectively, we show that OFC contains several functional clusters of neurons distinctly encoding cue-reward memory representations, with only select responses routed downstream to VTA. Surprisingly, these representations were stably maintained by the same neurons even after extinction of the cue-reward pairing, and supported behavioral learning and memory. Thus, OFC neuronal activity represents a long-term cue-reward associative memory to support behavioral adaptation. |
format | Online Article Text |
id | pubmed-7002110 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
record_format | MEDLINE/PubMed |
spelling | pubmed-70021102020-02-05 Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation Namboodiri, Vijay Mohan K. Otis, James M. van Heeswijk, Kay Voets, Elisa S. Alghorazi, Rizk A. Rodriguez-Romaguera, Jose Mihalas, Stefan Stuber, Garret D. Nat Neurosci Article Learning to predict rewards based on environmental cues is essential for survival. The orbitofrontal cortex (OFC) contributes to such learning, by conveying reward-related information to brain areas such as the ventral tegmental area (VTA). Despite this, how cue-reward memory representations form in individual OFC neurons and are modified based on new information is unknown. To address this, using in vivo 2-photon calcium imaging in mice, we tracked the response evolution of thousands of OFC output neurons, including those projecting to VTA, through multiple days and stages of cue-reward learning. Collectively, we show that OFC contains several functional clusters of neurons distinctly encoding cue-reward memory representations, with only select responses routed downstream to VTA. Surprisingly, these representations were stably maintained by the same neurons even after extinction of the cue-reward pairing, and supported behavioral learning and memory. Thus, OFC neuronal activity represents a long-term cue-reward associative memory to support behavioral adaptation. 2019-06-03 2019-07 /pmc/articles/PMC7002110/ /pubmed/31160741 http://dx.doi.org/10.1038/s41593-019-0408-1 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Namboodiri, Vijay Mohan K. Otis, James M. van Heeswijk, Kay Voets, Elisa S. Alghorazi, Rizk A. Rodriguez-Romaguera, Jose Mihalas, Stefan Stuber, Garret D. Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title | Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title_full | Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title_fullStr | Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title_full_unstemmed | Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title_short | Single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
title_sort | single-cell activity tracking reveals that orbitofrontal neurons acquire and maintain a long-term memory to guide behavioral adaptation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7002110/ https://www.ncbi.nlm.nih.gov/pubmed/31160741 http://dx.doi.org/10.1038/s41593-019-0408-1 |
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