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Dopamine and serotonin interplay for valence-based spatial learning
Dopamine (DA) and serotonin (5-HT) are important neuromodulators of synaptic plasticity that have been linked to learning from positive or negative outcomes or valence-based learning. In the hippocampus, both affect long-term plasticity but play different roles in encoding uncertainty or predicted r...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620746/ https://www.ncbi.nlm.nih.gov/pubmed/35417691 http://dx.doi.org/10.1016/j.celrep.2022.110645 |
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author | Wert-Carvajal, Carlos Reneaux, Melissa Tchumatchenko, Tatjana Clopath, Claudia |
author_facet | Wert-Carvajal, Carlos Reneaux, Melissa Tchumatchenko, Tatjana Clopath, Claudia |
author_sort | Wert-Carvajal, Carlos |
collection | PubMed |
description | Dopamine (DA) and serotonin (5-HT) are important neuromodulators of synaptic plasticity that have been linked to learning from positive or negative outcomes or valence-based learning. In the hippocampus, both affect long-term plasticity but play different roles in encoding uncertainty or predicted reward. DA has been related to positive valence, from reward consumption or avoidance behavior, and 5-HT to aversive encoding. We propose DA produces overall LTP while 5-HT elicits LTD. Here, we compare two reward-modulated spike timing-dependent plasticity (R-STDP) rules to describe the action of these neuromodulators. We examined their role in cognitive performance and flexibility for computational models of the Morris water maze task and reversal learning. Our results show that the interplay of DA and 5-HT improves learning performance and can explain experimental evidence. This study reinforces the importance of neuromodulation in determining the direction of plasticity. |
format | Online Article Text |
id | pubmed-9620746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-96207462022-11-02 Dopamine and serotonin interplay for valence-based spatial learning Wert-Carvajal, Carlos Reneaux, Melissa Tchumatchenko, Tatjana Clopath, Claudia Cell Rep Report Dopamine (DA) and serotonin (5-HT) are important neuromodulators of synaptic plasticity that have been linked to learning from positive or negative outcomes or valence-based learning. In the hippocampus, both affect long-term plasticity but play different roles in encoding uncertainty or predicted reward. DA has been related to positive valence, from reward consumption or avoidance behavior, and 5-HT to aversive encoding. We propose DA produces overall LTP while 5-HT elicits LTD. Here, we compare two reward-modulated spike timing-dependent plasticity (R-STDP) rules to describe the action of these neuromodulators. We examined their role in cognitive performance and flexibility for computational models of the Morris water maze task and reversal learning. Our results show that the interplay of DA and 5-HT improves learning performance and can explain experimental evidence. This study reinforces the importance of neuromodulation in determining the direction of plasticity. Cell Press 2022-04-13 /pmc/articles/PMC9620746/ /pubmed/35417691 http://dx.doi.org/10.1016/j.celrep.2022.110645 Text en © 2022 The Authors https://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 | Report Wert-Carvajal, Carlos Reneaux, Melissa Tchumatchenko, Tatjana Clopath, Claudia Dopamine and serotonin interplay for valence-based spatial learning |
title | Dopamine and serotonin interplay for valence-based spatial learning |
title_full | Dopamine and serotonin interplay for valence-based spatial learning |
title_fullStr | Dopamine and serotonin interplay for valence-based spatial learning |
title_full_unstemmed | Dopamine and serotonin interplay for valence-based spatial learning |
title_short | Dopamine and serotonin interplay for valence-based spatial learning |
title_sort | dopamine and serotonin interplay for valence-based spatial learning |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9620746/ https://www.ncbi.nlm.nih.gov/pubmed/35417691 http://dx.doi.org/10.1016/j.celrep.2022.110645 |
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