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Inhibitory learning of phototaxis by honeybees in a passive-avoidance task

Honeybees are a standard model for the study of appetitive learning and memory. Yet, fewer attempts have been performed to characterize aversive learning and memory in this insect and uncover its molecular underpinnings. Here, we took advantage of the positive phototactic behavior of bees kept away...

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Autores principales: Marchal, Paul, Villar, Maria Eugenia, Geng, Haiyang, Arrufat, Patrick, Combe, Maud, Viola, Haydée, Massou, Isabelle, Giurfa, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749929/
https://www.ncbi.nlm.nih.gov/pubmed/31527185
http://dx.doi.org/10.1101/lm.050120.119
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author Marchal, Paul
Villar, Maria Eugenia
Geng, Haiyang
Arrufat, Patrick
Combe, Maud
Viola, Haydée
Massou, Isabelle
Giurfa, Martin
author_facet Marchal, Paul
Villar, Maria Eugenia
Geng, Haiyang
Arrufat, Patrick
Combe, Maud
Viola, Haydée
Massou, Isabelle
Giurfa, Martin
author_sort Marchal, Paul
collection PubMed
description Honeybees are a standard model for the study of appetitive learning and memory. Yet, fewer attempts have been performed to characterize aversive learning and memory in this insect and uncover its molecular underpinnings. Here, we took advantage of the positive phototactic behavior of bees kept away from the hive in a dark environment and established a passive-avoidance task in which they had to suppress positive phototaxis. Bees placed in a two-compartment box learned to inhibit spontaneous attraction to a compartment illuminated with blue light by associating and entering into that chamber with shock delivery. Inhibitory learning resulted in an avoidance memory that could be retrieved 24 h after training and that was specific to the punished blue light. The memory was mainly operant but involved a Pavlovian component linking the blue light and the shock. Coupling conditioning with transcriptional analyses in key areas of the brain showed that inhibitory learning of phototaxis leads to an up-regulation of the dopaminergic receptor gene Amdop1 in the calyces of the mushroom bodies, consistently with the role of dopamine signaling in different forms of aversive learning in insects. Our results thus introduce new perspectives for uncovering further cellular and molecular underpinnings of aversive learning and memory in bees. Overall, they represent an important step toward comparative learning studies between the appetitive and the aversive frameworks.
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spelling pubmed-67499292020-10-01 Inhibitory learning of phototaxis by honeybees in a passive-avoidance task Marchal, Paul Villar, Maria Eugenia Geng, Haiyang Arrufat, Patrick Combe, Maud Viola, Haydée Massou, Isabelle Giurfa, Martin Learn Mem Research Honeybees are a standard model for the study of appetitive learning and memory. Yet, fewer attempts have been performed to characterize aversive learning and memory in this insect and uncover its molecular underpinnings. Here, we took advantage of the positive phototactic behavior of bees kept away from the hive in a dark environment and established a passive-avoidance task in which they had to suppress positive phototaxis. Bees placed in a two-compartment box learned to inhibit spontaneous attraction to a compartment illuminated with blue light by associating and entering into that chamber with shock delivery. Inhibitory learning resulted in an avoidance memory that could be retrieved 24 h after training and that was specific to the punished blue light. The memory was mainly operant but involved a Pavlovian component linking the blue light and the shock. Coupling conditioning with transcriptional analyses in key areas of the brain showed that inhibitory learning of phototaxis leads to an up-regulation of the dopaminergic receptor gene Amdop1 in the calyces of the mushroom bodies, consistently with the role of dopamine signaling in different forms of aversive learning in insects. Our results thus introduce new perspectives for uncovering further cellular and molecular underpinnings of aversive learning and memory in bees. Overall, they represent an important step toward comparative learning studies between the appetitive and the aversive frameworks. Cold Spring Harbor Laboratory Press 2019-10 /pmc/articles/PMC6749929/ /pubmed/31527185 http://dx.doi.org/10.1101/lm.050120.119 Text en © 2019 Marchal et al.; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Research
Marchal, Paul
Villar, Maria Eugenia
Geng, Haiyang
Arrufat, Patrick
Combe, Maud
Viola, Haydée
Massou, Isabelle
Giurfa, Martin
Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title_full Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title_fullStr Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title_full_unstemmed Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title_short Inhibitory learning of phototaxis by honeybees in a passive-avoidance task
title_sort inhibitory learning of phototaxis by honeybees in a passive-avoidance task
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6749929/
https://www.ncbi.nlm.nih.gov/pubmed/31527185
http://dx.doi.org/10.1101/lm.050120.119
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