An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals

Detalhes bibliográficos
Autor(a) principal: Iigaya, Kiyohito
Data de Publicação: 2018
Outros Autores: Fonseca, Madalena S., Murakami, Masayoshi, Mainen, Zachary F., Dayan, Peter
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.26/39184
Resumo: Serotonin has widespread, but computationally obscure, modulatory effects on learning and cognition. Here, we studied the impact of optogenetic stimulation of dorsal raphe serotonin neurons in mice performing a non-stationary, reward-driven decision-making task. Animals showed two distinct choice strategies. Choices after short inter-trial-intervals (ITIs) depended only on the last trial outcome and followed a win-stay-lose-switch pattern. In contrast, choices after long ITIs reflected outcome history over multiple trials, as described by reinforcement learning models. We found that optogenetic stimulation during a trial significantly boosted the rate of learning that occurred due to the outcome of that trial, but these effects were only exhibited on choices after long ITIs. This suggests that serotonin neurons modulate reinforcement learning rates, and that this influence is masked by alternate, unaffected, decision mechanisms. These results provide insight into the role of serotonin in treating psychiatric disorders, particularly its modulation of neural plasticity and learning.
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spelling An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervalsSerotonin has widespread, but computationally obscure, modulatory effects on learning and cognition. Here, we studied the impact of optogenetic stimulation of dorsal raphe serotonin neurons in mice performing a non-stationary, reward-driven decision-making task. Animals showed two distinct choice strategies. Choices after short inter-trial-intervals (ITIs) depended only on the last trial outcome and followed a win-stay-lose-switch pattern. In contrast, choices after long ITIs reflected outcome history over multiple trials, as described by reinforcement learning models. We found that optogenetic stimulation during a trial significantly boosted the rate of learning that occurred due to the outcome of that trial, but these effects were only exhibited on choices after long ITIs. This suggests that serotonin neurons modulate reinforcement learning rates, and that this influence is masked by alternate, unaffected, decision mechanisms. These results provide insight into the role of serotonin in treating psychiatric disorders, particularly its modulation of neural plasticity and learning.ERC (250334 and 671251)Springer NatureRepositório ComumIigaya, KiyohitoFonseca, Madalena S.Murakami, MasayoshiMainen, Zachary F.Dayan, Peter2022-02-04T13:11:49Z2018-06-262018-06-26T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.26/39184enghttps://doi.org/10.1038/s41467-018-04840-2info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-04-26T17:15:15Zoai:comum.rcaap.pt:10400.26/39184Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T15:49:01.815753Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
title An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
spellingShingle An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
Iigaya, Kiyohito
title_short An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
title_full An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
title_fullStr An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
title_full_unstemmed An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
title_sort An effect of serotonergic stimulation on learning rates for rewards apparent after long intertrial intervals
author Iigaya, Kiyohito
author_facet Iigaya, Kiyohito
Fonseca, Madalena S.
Murakami, Masayoshi
Mainen, Zachary F.
Dayan, Peter
author_role author
author2 Fonseca, Madalena S.
Murakami, Masayoshi
Mainen, Zachary F.
Dayan, Peter
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Repositório Comum
dc.contributor.author.fl_str_mv Iigaya, Kiyohito
Fonseca, Madalena S.
Murakami, Masayoshi
Mainen, Zachary F.
Dayan, Peter
description Serotonin has widespread, but computationally obscure, modulatory effects on learning and cognition. Here, we studied the impact of optogenetic stimulation of dorsal raphe serotonin neurons in mice performing a non-stationary, reward-driven decision-making task. Animals showed two distinct choice strategies. Choices after short inter-trial-intervals (ITIs) depended only on the last trial outcome and followed a win-stay-lose-switch pattern. In contrast, choices after long ITIs reflected outcome history over multiple trials, as described by reinforcement learning models. We found that optogenetic stimulation during a trial significantly boosted the rate of learning that occurred due to the outcome of that trial, but these effects were only exhibited on choices after long ITIs. This suggests that serotonin neurons modulate reinforcement learning rates, and that this influence is masked by alternate, unaffected, decision mechanisms. These results provide insight into the role of serotonin in treating psychiatric disorders, particularly its modulation of neural plasticity and learning.
publishDate 2018
dc.date.none.fl_str_mv 2018-06-26
2018-06-26T00:00:00Z
2022-02-04T13:11:49Z
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