Optogenetic activation of mesencephalic projections to the nucleus accumbens shell impairs probabilistic reversal learning by disrupting learning from negative reinforcement

Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and Parkinson's disease. Putative neural substrates of cognitive flexibility include mesencephalic pathways to the ventral striatum (VS) and d...

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Published inThe European journal of neuroscience Vol. 60; no. 11; pp. 6765 - 6778
Main Authors Zühlsdorff, Katharina, Sala‐Bayo, Júlia, Piller, Sammy, Zhukovsky, Peter, Lamla, Thorsten, Nissen, Wiebke, Heimendahl, Moritz, Deiana, Serena, Nicholson, Janet R., Robbins, Trevor W., Alsiö, Johan, Dalley, Jeffrey W.
Format Journal Article
LanguageEnglish
Published France Wiley Subscription Services, Inc 01.12.2024
John Wiley and Sons Inc
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Abstract Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and Parkinson's disease. Putative neural substrates of cognitive flexibility include mesencephalic pathways to the ventral striatum (VS) and dorsomedial striatum (DMS), hypothesized to encode learning signals needed to maximize rewarded outcomes during decision‐making. However, it is unclear whether mesencephalic projections to the ventral and dorsal striatum are distinct in their contribution to flexible reward‐related learning. Here, rats acquired a two‐choice spatial probabilistic reversal learning (PRL) task, reinforced on an 80%|20% basis (correct|incorrect responses) that assessed the flexibility of behaviour to repeated reversals of response‐outcome contingencies. We report that optogenetic stimulation of projections from the ventral tegmental area (VTA) to the nucleus accumbens shell (NAcS) in the VS significantly impaired reversal learning when optical stimulation was temporally aligned with negative feedback (i.e., reward omission). VTA → NAcS stimulation during other phases of the behavioural task was without significant effect. Optogenetic stimulation of projection neurons from the substantia nigra (SN) to the DMS, aligned either with reward receipt or omission or prior to making a choice, had no significant effect on reversal learning. These findings are consistent with the notion that increased activity in the VTA → NAcS pathway disrupts behavioural flexibility by impairing learning from negative reinforcement.
AbstractList Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and Parkinson's disease. Putative neural substrates of cognitive flexibility include mesencephalic pathways to the ventral striatum (VS) and dorsomedial striatum (DMS), hypothesized to encode learning signals needed to maximize rewarded outcomes during decision-making. However, it is unclear whether mesencephalic projections to the ventral and dorsal striatum are distinct in their contribution to flexible reward-related learning. Here, rats acquired a two-choice spatial probabilistic reversal learning (PRL) task, reinforced on an 80%|20% basis (correct|incorrect responses) that assessed the flexibility of behaviour to repeated reversals of response-outcome contingencies. We report that optogenetic stimulation of projections from the ventral tegmental area (VTA) to the nucleus accumbens shell (NAcS) in the VS significantly impaired reversal learning when optical stimulation was temporally aligned with negative feedback (i.e., reward omission). VTA → NAcS stimulation during other phases of the behavioural task was without significant effect. Optogenetic stimulation of projection neurons from the substantia nigra (SN) to the DMS, aligned either with reward receipt or omission or prior to making a choice, had no significant effect on reversal learning. These findings are consistent with the notion that increased activity in the VTA → NAcS pathway disrupts behavioural flexibility by impairing learning from negative reinforcement.
Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and Parkinson's disease. Putative neural substrates of cognitive flexibility include mesencephalic pathways to the ventral striatum (VS) and dorsomedial striatum (DMS), hypothesized to encode learning signals needed to maximize rewarded outcomes during decision-making. However, it is unclear whether mesencephalic projections to the ventral and dorsal striatum are distinct in their contribution to flexible reward-related learning. Here, rats acquired a two-choice spatial probabilistic reversal learning (PRL) task, reinforced on an 80%|20% basis (correct|incorrect responses) that assessed the flexibility of behaviour to repeated reversals of response-outcome contingencies. We report that optogenetic stimulation of projections from the ventral tegmental area (VTA) to the nucleus accumbens shell (NAcS) in the VS significantly impaired reversal learning when optical stimulation was temporally aligned with negative feedback (i.e., reward omission). VTA → NAcS stimulation during other phases of the behavioural task was without significant effect. Optogenetic stimulation of projection neurons from the substantia nigra (SN) to the DMS, aligned either with reward receipt or omission or prior to making a choice, had no significant effect on reversal learning. These findings are consistent with the notion that increased activity in the VTA → NAcS pathway disrupts behavioural flexibility by impairing learning from negative reinforcement.Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and Parkinson's disease. Putative neural substrates of cognitive flexibility include mesencephalic pathways to the ventral striatum (VS) and dorsomedial striatum (DMS), hypothesized to encode learning signals needed to maximize rewarded outcomes during decision-making. However, it is unclear whether mesencephalic projections to the ventral and dorsal striatum are distinct in their contribution to flexible reward-related learning. Here, rats acquired a two-choice spatial probabilistic reversal learning (PRL) task, reinforced on an 80%|20% basis (correct|incorrect responses) that assessed the flexibility of behaviour to repeated reversals of response-outcome contingencies. We report that optogenetic stimulation of projections from the ventral tegmental area (VTA) to the nucleus accumbens shell (NAcS) in the VS significantly impaired reversal learning when optical stimulation was temporally aligned with negative feedback (i.e., reward omission). VTA → NAcS stimulation during other phases of the behavioural task was without significant effect. Optogenetic stimulation of projection neurons from the substantia nigra (SN) to the DMS, aligned either with reward receipt or omission or prior to making a choice, had no significant effect on reversal learning. These findings are consistent with the notion that increased activity in the VTA → NAcS pathway disrupts behavioural flexibility by impairing learning from negative reinforcement.
Author Nissen, Wiebke
Heimendahl, Moritz
Robbins, Trevor W.
Dalley, Jeffrey W.
Zühlsdorff, Katharina
Zhukovsky, Peter
Deiana, Serena
Nicholson, Janet R.
Piller, Sammy
Lamla, Thorsten
Sala‐Bayo, Júlia
Alsiö, Johan
AuthorAffiliation 4 Present address: School of Physiology, Pharmacology and Neuroscience University of Bristol Bristol UK
1 Department of Psychology University of Cambridge Cambridge UK
3 Department of Psychiatry, Herchel Smith Building for Brain & Mind Sciences University of Cambridge Cambridge UK
2 Boehringer Ingelheim Pharma GmbH & Co. KG, Div. Research Germany Biberach an der Riß Germany
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Issue 11
Keywords striatum
cognitive flexibility
dopamine
negative feedback
optogenetics
Language English
License Attribution
2024 The Author(s). European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd.
This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
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Notes Funding information
Katharina Zühlsdorff and Júlia Sala‐Bayo, Joint first authors.
This research was funded by an award from Boehringer Ingelheim to JWD and by a Wellcome Trust Senior Investigator grant 104631/Z/14/Z to TWR. For the purpose of open access, the author has applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission. All experiments were conducted at Boehringer Ingelheim, Germany. This work was also supported by the La Caixa Foundation, Spain, and a studentship from Boehringer Ingelheim Pharma GmbH, Germany. KZ was funded by the Angharad Dodds John Bursary, Downing College, Cambridge. SP was funded by a student internship from Boehringer Ingelheim Pharma GmbH & Co. KG, Germany. SD, WN, MvH and JRN are full‐time employees at Boehringer Ingelheim Pharma GmbH, Germany. JWD has received funding from GlaxoSmithKline and editorial honoraria from the British Neuroscience Association and Springer Verlag. TWR is a consultant for Cambridge Cognition; had recent research grants with Shionogi and GlaxoSmithKline and receives editorial honoraria from Springer Nature and Elsevier.
Edited by: Serge Schiffmann
Johan Alsiö and Jeffrey W. Dalley, Joint last authors.
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Funding information This research was funded by an award from Boehringer Ingelheim to JWD and by a Wellcome Trust Senior Investigator grant 104631/Z/14/Z to TWR. For the purpose of open access, the author has applied a CC BY public copyright licence to any Author Accepted Manuscript version arising from this submission. All experiments were conducted at Boehringer Ingelheim, Germany. This work was also supported by the La Caixa Foundation, Spain, and a studentship from Boehringer Ingelheim Pharma GmbH, Germany. KZ was funded by the Angharad Dodds John Bursary, Downing College, Cambridge. SP was funded by a student internship from Boehringer Ingelheim Pharma GmbH & Co. KG, Germany. SD, WN, MvH and JRN are full‐time employees at Boehringer Ingelheim Pharma GmbH, Germany. JWD has received funding from GlaxoSmithKline and editorial honoraria from the British Neuroscience Association and Springer Verlag. TWR is a consultant for Cambridge Cognition; had recent research grants with Shionogi and GlaxoSmithKline and receives editorial honoraria from Springer Nature and Elsevier.
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Snippet Cognitive flexibility, the capacity to adapt behaviour to changes in the environment, is impaired in a range of brain disorders, including schizophrenia and...
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StartPage 6765
SubjectTerms Animals
Caudate-putamen
Choice learning
cognitive flexibility
Decision making
dopamine
Flexibility
Male
Mental disorders
Mesencephalon - physiology
Movement disorders
negative feedback
Neostriatum
Neural Pathways - physiology
Neurodegenerative diseases
Nucleus accumbens
Nucleus Accumbens - physiology
optogenetics
Optogenetics - methods
Parkinson's disease
Rats
Rats, Long-Evans
Reinforcement
Reinforcement, Psychology
Reversal learning
Reversal Learning - physiology
Reward
Schizophrenia
Short Communication
Spatial discrimination learning
striatum
Substantia nigra
Substantia Nigra - physiology
Ventral Tegmental Area - physiology
Ventral tegmentum
Title Optogenetic activation of mesencephalic projections to the nucleus accumbens shell impairs probabilistic reversal learning by disrupting learning from negative reinforcement
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fejn.16584
https://www.ncbi.nlm.nih.gov/pubmed/39479888
https://www.proquest.com/docview/3135037657
https://www.proquest.com/docview/3122644681
https://pubmed.ncbi.nlm.nih.gov/PMC11612850
Volume 60
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