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...
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Published in | Cell reports (Cambridge) Vol. 18; no. 4; pp. 905 - 917 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
24.01.2017
Cell Press Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 2211-1247 2211-1247 |
DOI | 10.1016/j.celrep.2016.12.085 |
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Abstract | 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.
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•Acetylcholine release is coordinated in prefrontal cortex and hippocampus•Tonic and phasic release are maximal during training on a cognitive task•Tonic acetylcholine release during REM sleep predicts subsequent wakefulness•Phasic acetylcholine release is preferentially associated with reward
In this study, Teles-Grilo Ruivo et al. use biosensors to simultaneously measure the release profiles of the neuromodulator acetylcholine in the prefrontal cortex and hippocampus of mice. They find that release on both tonic and phasic timescales is remarkably coordinated between brain regions and dependent on behavioral state. |
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AbstractList | 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.
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Acetylcholine release is coordinated in prefrontal cortex and hippocampus
•
Tonic and phasic release are maximal during training on a cognitive task
•
Tonic acetylcholine release during REM sleep predicts subsequent wakefulness
•
Phasic acetylcholine release is preferentially associated with reward
In this study, Teles-Grilo Ruivo et al. use biosensors to simultaneously measure the release profiles of the neuromodulator acetylcholine in the prefrontal cortex and hippocampus of mice. They find that release on both tonic and phasic timescales is remarkably coordinated between brain regions and dependent on behavioral state. 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. 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. 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. [Display omitted] •Acetylcholine release is coordinated in prefrontal cortex and hippocampus•Tonic and phasic release are maximal during training on a cognitive task•Tonic acetylcholine release during REM sleep predicts subsequent wakefulness•Phasic acetylcholine release is preferentially associated with reward In this study, Teles-Grilo Ruivo et al. use biosensors to simultaneously measure the release profiles of the neuromodulator acetylcholine in the prefrontal cortex and hippocampus of mice. They find that release on both tonic and phasic timescales is remarkably coordinated between brain regions and dependent on behavioral state. |
Author | Lowry, John P. Conway, Michael W. Kinsley, Peter J. Gilmour, Gary Baker, Keeley L. Isaac, John T.R. Phillips, Keith G. Mellor, Jack R. Teles-Grilo Ruivo, Leonor M. |
AuthorAffiliation | 3 Department of Chemistry, Maynooth University, Co. Kildare, Ireland 1 Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK 2 Centre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol BS8 1TD, UK |
AuthorAffiliation_xml | – name: 1 Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – name: 2 Centre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol BS8 1TD, UK – name: 3 Department of Chemistry, Maynooth University, Co. Kildare, Ireland |
Author_xml | – sequence: 1 givenname: Leonor M. surname: Teles-Grilo Ruivo fullname: Teles-Grilo Ruivo, Leonor M. organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 2 givenname: Keeley L. surname: Baker fullname: Baker, Keeley L. organization: Department of Chemistry, Maynooth University, Co. Kildare, Ireland – sequence: 3 givenname: Michael W. surname: Conway fullname: Conway, Michael W. organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 4 givenname: Peter J. surname: Kinsley fullname: Kinsley, Peter J. organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 5 givenname: Gary surname: Gilmour fullname: Gilmour, Gary organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 6 givenname: Keith G. surname: Phillips fullname: Phillips, Keith G. organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 7 givenname: John T.R. surname: Isaac fullname: Isaac, John T.R. organization: Lilly Centre for Cognitive Neuroscience, Eli Lilly and Company Ltd., Erl Wood Manor, Windlesham, Surrey GU20 6PH, UK – sequence: 8 givenname: John P. surname: Lowry fullname: Lowry, John P. email: john.lowry@nuim.ie organization: Department of Chemistry, Maynooth University, Co. Kildare, Ireland – sequence: 9 givenname: Jack R. surname: Mellor fullname: Mellor, Jack R. email: jack.mellor@bristol.ac.uk organization: Centre for Synaptic Plasticity, School of Physiology, Pharmacology and Neuroscience, University of Bristol, Bristol BS8 1TD, UK |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28122241$$D View this record in MEDLINE/PubMed |
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SubjectTerms | acetylcholine Acetylcholine - analysis Acetylcholine - metabolism Animals Arousal Behavior, Animal Biosensing Techniques biosensor Electrochemical Techniques Electrodes, Implanted hippocampus Hippocampus - metabolism Hippocampus - pathology Locomotion Male Maze Learning Memory, Short-Term Mice Mice, Inbred C57BL prefrontal cortex Prefrontal Cortex - metabolism Prefrontal Cortex - pathology Reward Sleep, REM Wakefulness |
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Title | Coordinated Acetylcholine Release in Prefrontal Cortex and Hippocampus Is Associated with Arousal and Reward on Distinct Timescales |
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