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Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales
Cholinergic neurotransmission throughout the neocortex and hippocampus regulates arousal, learning, and attention. However, owing to the poorly characterized timing and location of acetylcholine release, its detailed behavioral functions remain unclear. Using electrochemical biosensors chronically i...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289927/ https://www.ncbi.nlm.nih.gov/pubmed/28122241 http://dx.doi.org/10.1016/j.celrep.2016.12.085 |
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author | Teles-Grilo Ruivo, Leonor M. Baker, Keeley L. Conway, Michael W. Kinsley, Peter J. Gilmour, Gary Phillips, Keith G. Isaac, John T.R. Lowry, John P. Mellor, Jack R. |
author_facet | Teles-Grilo Ruivo, Leonor M. Baker, Keeley L. Conway, Michael W. Kinsley, Peter J. Gilmour, Gary Phillips, Keith G. Isaac, John T.R. Lowry, John P. Mellor, Jack R. |
author_sort | Teles-Grilo Ruivo, Leonor M. |
collection | PubMed |
description | Cholinergic neurotransmission throughout the neocortex and hippocampus regulates arousal, learning, and attention. However, owing to the poorly characterized timing and location of acetylcholine release, its detailed behavioral functions remain unclear. Using electrochemical biosensors chronically implanted in mice, we made continuous measurements of the spatiotemporal dynamics of acetylcholine release across multiple behavioral states. We found that tonic levels of acetylcholine release were coordinated between the prefrontal cortex and hippocampus and maximal during training on a rewarded working memory task. Tonic release also increased during REM sleep but was contingent on subsequent wakefulness. In contrast, coordinated phasic acetylcholine release occurred only during the memory task and was strongly localized to reward delivery areas without being contingent on trial outcome. These results show that coordinated acetylcholine release between the prefrontal cortex and hippocampus is associated with reward and arousal on distinct timescales, providing dual mechanisms to support learned behavior acquisition during cognitive task performance. |
format | Online Article Text |
id | pubmed-5289927 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-52899272017-02-13 Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales Teles-Grilo Ruivo, Leonor M. Baker, Keeley L. Conway, Michael W. Kinsley, Peter J. Gilmour, Gary Phillips, Keith G. Isaac, John T.R. Lowry, John P. Mellor, Jack R. Cell Rep Article Cholinergic neurotransmission throughout the neocortex and hippocampus regulates arousal, learning, and attention. However, owing to the poorly characterized timing and location of acetylcholine release, its detailed behavioral functions remain unclear. Using electrochemical biosensors chronically implanted in mice, we made continuous measurements of the spatiotemporal dynamics of acetylcholine release across multiple behavioral states. We found that tonic levels of acetylcholine release were coordinated between the prefrontal cortex and hippocampus and maximal during training on a rewarded working memory task. Tonic release also increased during REM sleep but was contingent on subsequent wakefulness. In contrast, coordinated phasic acetylcholine release occurred only during the memory task and was strongly localized to reward delivery areas without being contingent on trial outcome. These results show that coordinated acetylcholine release between the prefrontal cortex and hippocampus is associated with reward and arousal on distinct timescales, providing dual mechanisms to support learned behavior acquisition during cognitive task performance. Cell Press 2017-01-24 /pmc/articles/PMC5289927/ /pubmed/28122241 http://dx.doi.org/10.1016/j.celrep.2016.12.085 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Teles-Grilo Ruivo, Leonor M. Baker, Keeley L. Conway, Michael W. Kinsley, Peter J. Gilmour, Gary Phillips, Keith G. Isaac, John T.R. Lowry, John P. Mellor, Jack R. Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title_full | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title_fullStr | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title_full_unstemmed | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title_short | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
title_sort | coordinated acetylcholine release in prefrontal cortex and hippocampus is associated with arousal and reward on distinct timescales |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5289927/ https://www.ncbi.nlm.nih.gov/pubmed/28122241 http://dx.doi.org/10.1016/j.celrep.2016.12.085 |
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