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Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning
Our understanding of how value-related information is encoded in the ventral tegmental area (VTA) is based mainly on the responses of individual putative dopamine neurons. In contrast to cortical areas, the nature of coordinated interactions between groups of VTA neurons during motivated behavior is...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253108/ https://www.ncbi.nlm.nih.gov/pubmed/22238652 http://dx.doi.org/10.1371/journal.pone.0029766 |
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author | Kim, Yunbok Wood, Jesse Moghaddam, Bita |
author_facet | Kim, Yunbok Wood, Jesse Moghaddam, Bita |
author_sort | Kim, Yunbok |
collection | PubMed |
description | Our understanding of how value-related information is encoded in the ventral tegmental area (VTA) is based mainly on the responses of individual putative dopamine neurons. In contrast to cortical areas, the nature of coordinated interactions between groups of VTA neurons during motivated behavior is largely unknown. These interactions can strongly affect information processing, highlighting the importance of investigating network level activity. We recorded the activity of multiple single units and local field potentials (LFP) in the VTA during a task in which rats learned to associate novel stimuli with different outcomes. We found that coordinated activity of VTA units with either putative dopamine or GABA waveforms was influenced differently by rewarding versus aversive outcomes. Specifically, after learning, stimuli paired with a rewarding outcome increased the correlation in activity levels between unit pairs whereas stimuli paired with an aversive outcome decreased the correlation. Paired single unit responses also became more redundant after learning. These response patterns flexibly tracked the reversal of contingencies, suggesting that learning is associated with changing correlations and enhanced functional connectivity between VTA neurons. Analysis of LFP recorded simultaneously with unit activity showed an increase in the power of theta oscillations when stimuli predicted reward but not an aversive outcome. With learning, a higher proportion of putative GABA units were phase locked to the theta oscillations than putative dopamine units. These patterns also adapted when task contingencies were changed. Taken together, these data demonstrate that VTA neurons organize flexibly as functional networks to support appetitive and aversive learning. |
format | Online Article Text |
id | pubmed-3253108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-32531082012-01-11 Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning Kim, Yunbok Wood, Jesse Moghaddam, Bita PLoS One Research Article Our understanding of how value-related information is encoded in the ventral tegmental area (VTA) is based mainly on the responses of individual putative dopamine neurons. In contrast to cortical areas, the nature of coordinated interactions between groups of VTA neurons during motivated behavior is largely unknown. These interactions can strongly affect information processing, highlighting the importance of investigating network level activity. We recorded the activity of multiple single units and local field potentials (LFP) in the VTA during a task in which rats learned to associate novel stimuli with different outcomes. We found that coordinated activity of VTA units with either putative dopamine or GABA waveforms was influenced differently by rewarding versus aversive outcomes. Specifically, after learning, stimuli paired with a rewarding outcome increased the correlation in activity levels between unit pairs whereas stimuli paired with an aversive outcome decreased the correlation. Paired single unit responses also became more redundant after learning. These response patterns flexibly tracked the reversal of contingencies, suggesting that learning is associated with changing correlations and enhanced functional connectivity between VTA neurons. Analysis of LFP recorded simultaneously with unit activity showed an increase in the power of theta oscillations when stimuli predicted reward but not an aversive outcome. With learning, a higher proportion of putative GABA units were phase locked to the theta oscillations than putative dopamine units. These patterns also adapted when task contingencies were changed. Taken together, these data demonstrate that VTA neurons organize flexibly as functional networks to support appetitive and aversive learning. Public Library of Science 2012-01-06 /pmc/articles/PMC3253108/ /pubmed/22238652 http://dx.doi.org/10.1371/journal.pone.0029766 Text en Kim et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kim, Yunbok Wood, Jesse Moghaddam, Bita Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title | Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title_full | Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title_fullStr | Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title_full_unstemmed | Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title_short | Coordinated Activity of Ventral Tegmental Neurons Adapts to Appetitive and Aversive Learning |
title_sort | coordinated activity of ventral tegmental neurons adapts to appetitive and aversive learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3253108/ https://www.ncbi.nlm.nih.gov/pubmed/22238652 http://dx.doi.org/10.1371/journal.pone.0029766 |
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