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Re-evaluation of learned information in Drosophila
Animals constantly reassess the reliability of learned information to optimize their behavior. On retrieval, consolidated long-term memory can be neutralized by extinction if the learned prediction was inaccurate 1. Alternatively, retrieved memory can be maintained, following a period of reconsolida...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392358/ https://www.ncbi.nlm.nih.gov/pubmed/28379939 http://dx.doi.org/10.1038/nature21716 |
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author | Felsenberg, Johannes Barnstedt, Oliver Cognigni, Paola Lin, Suewei Waddell, Scott |
author_facet | Felsenberg, Johannes Barnstedt, Oliver Cognigni, Paola Lin, Suewei Waddell, Scott |
author_sort | Felsenberg, Johannes |
collection | PubMed |
description | Animals constantly reassess the reliability of learned information to optimize their behavior. On retrieval, consolidated long-term memory can be neutralized by extinction if the learned prediction was inaccurate 1. Alternatively, retrieved memory can be maintained, following a period of reconsolidation during which it is labile 2. Although extinction and reconsolidation provide opportunities to alleviate problematic human memories 3–5, we lack a detailed mechanistic understanding of memory updating processes. Here we identify neural operations underpinning re-evaluation of memory in Drosophila. Reactivation of sugar-reinforced olfactory memory can lead to either extinction or reconsolidation, depending on prediction accuracy. Each process recruits activity in specific parts of the mushroom body output network and distinct subsets of reinforcing dopaminergic neurons. Memory extinction requires output neurons with dendrites in the α and α′ lobes of the mushroom body, which drive negatively reinforcing dopaminergic neurons that innervate neighbouring zones. The aversive valence of these new extinction memories neutralizes previously learned odor preference. Memory reconsolidation requires the γ2α′ 1 mushroom body output neurons. This pathway recruits negatively reinforcing dopaminergic neurons innervating the same compartment and re-engages positively reinforcing dopaminergic neurons to reconsolidate the original reward memory. These data establish that recurrent and hierarchical connectivity between mushroom body output neurons and dopaminergic neurons enables memory re-evaluation driven by reward prediction error. |
format | Online Article Text |
id | pubmed-5392358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-53923582017-10-05 Re-evaluation of learned information in Drosophila Felsenberg, Johannes Barnstedt, Oliver Cognigni, Paola Lin, Suewei Waddell, Scott Nature Article Animals constantly reassess the reliability of learned information to optimize their behavior. On retrieval, consolidated long-term memory can be neutralized by extinction if the learned prediction was inaccurate 1. Alternatively, retrieved memory can be maintained, following a period of reconsolidation during which it is labile 2. Although extinction and reconsolidation provide opportunities to alleviate problematic human memories 3–5, we lack a detailed mechanistic understanding of memory updating processes. Here we identify neural operations underpinning re-evaluation of memory in Drosophila. Reactivation of sugar-reinforced olfactory memory can lead to either extinction or reconsolidation, depending on prediction accuracy. Each process recruits activity in specific parts of the mushroom body output network and distinct subsets of reinforcing dopaminergic neurons. Memory extinction requires output neurons with dendrites in the α and α′ lobes of the mushroom body, which drive negatively reinforcing dopaminergic neurons that innervate neighbouring zones. The aversive valence of these new extinction memories neutralizes previously learned odor preference. Memory reconsolidation requires the γ2α′ 1 mushroom body output neurons. This pathway recruits negatively reinforcing dopaminergic neurons innervating the same compartment and re-engages positively reinforcing dopaminergic neurons to reconsolidate the original reward memory. These data establish that recurrent and hierarchical connectivity between mushroom body output neurons and dopaminergic neurons enables memory re-evaluation driven by reward prediction error. 2017-04-05 2017-04-13 /pmc/articles/PMC5392358/ /pubmed/28379939 http://dx.doi.org/10.1038/nature21716 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Felsenberg, Johannes Barnstedt, Oliver Cognigni, Paola Lin, Suewei Waddell, Scott Re-evaluation of learned information in Drosophila |
title | Re-evaluation of learned information in Drosophila |
title_full | Re-evaluation of learned information in Drosophila |
title_fullStr | Re-evaluation of learned information in Drosophila |
title_full_unstemmed | Re-evaluation of learned information in Drosophila |
title_short | Re-evaluation of learned information in Drosophila |
title_sort | re-evaluation of learned information in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5392358/ https://www.ncbi.nlm.nih.gov/pubmed/28379939 http://dx.doi.org/10.1038/nature21716 |
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