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Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila

Survival in many animals requires the ability to associate certain cues with danger and others with safety. In a Drosophila melanogaster aversive olfactory conditioning paradigm, flies are exposed to two odours, one presented coincidentally with electrical shocks, and a second presented 45 s after s...

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Autores principales: Naganos, Shintaro, Ueno, Kohei, Horiuchi, Junjiro, Saitoe, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540629/
https://www.ncbi.nlm.nih.gov/pubmed/35815601
http://dx.doi.org/10.1111/ejn.15766
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author Naganos, Shintaro
Ueno, Kohei
Horiuchi, Junjiro
Saitoe, Minoru
author_facet Naganos, Shintaro
Ueno, Kohei
Horiuchi, Junjiro
Saitoe, Minoru
author_sort Naganos, Shintaro
collection PubMed
description Survival in many animals requires the ability to associate certain cues with danger and others with safety. In a Drosophila melanogaster aversive olfactory conditioning paradigm, flies are exposed to two odours, one presented coincidentally with electrical shocks, and a second presented 45 s after shock cessation. When flies are later given a choice between these two odours, they avoid the shock‐paired odour and prefer the unpaired odour. While many studies have examined how flies learn to avoid the shock‐paired odour through formation of odour‐fear associations, here we demonstrate that conditioning also causes flies to actively approach the second odour. In contrast to fear memories, which are longer lasting and requires activity of D1‐like dopamine receptors only in the mushroom bodies, approach memory is short‐lasting and requires activity of D1‐like dopamine receptors in projection neurons originating from the antennal lobes, primary olfactory centers. Further, while recall of fear memories requires activity of the mushroom bodies, recall of approach memories does not. Our data suggest that olfactory approach memory is formed using different mechanisms in different brain locations compared to aversive and appetitive olfactory memories.
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spelling pubmed-95406292022-10-14 Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila Naganos, Shintaro Ueno, Kohei Horiuchi, Junjiro Saitoe, Minoru Eur J Neurosci Cognitive Neuroscience Survival in many animals requires the ability to associate certain cues with danger and others with safety. In a Drosophila melanogaster aversive olfactory conditioning paradigm, flies are exposed to two odours, one presented coincidentally with electrical shocks, and a second presented 45 s after shock cessation. When flies are later given a choice between these two odours, they avoid the shock‐paired odour and prefer the unpaired odour. While many studies have examined how flies learn to avoid the shock‐paired odour through formation of odour‐fear associations, here we demonstrate that conditioning also causes flies to actively approach the second odour. In contrast to fear memories, which are longer lasting and requires activity of D1‐like dopamine receptors only in the mushroom bodies, approach memory is short‐lasting and requires activity of D1‐like dopamine receptors in projection neurons originating from the antennal lobes, primary olfactory centers. Further, while recall of fear memories requires activity of the mushroom bodies, recall of approach memories does not. Our data suggest that olfactory approach memory is formed using different mechanisms in different brain locations compared to aversive and appetitive olfactory memories. John Wiley and Sons Inc. 2022-07-17 2022-09 /pmc/articles/PMC9540629/ /pubmed/35815601 http://dx.doi.org/10.1111/ejn.15766 Text en © 2022 The Authors. European Journal of Neuroscience published by Federation of European Neuroscience Societies and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cognitive Neuroscience
Naganos, Shintaro
Ueno, Kohei
Horiuchi, Junjiro
Saitoe, Minoru
Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title_full Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title_fullStr Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title_full_unstemmed Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title_short Dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in Drosophila
title_sort dopamine activity in projection neurons regulates short‐lasting olfactory approach memory in drosophila
topic Cognitive Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540629/
https://www.ncbi.nlm.nih.gov/pubmed/35815601
http://dx.doi.org/10.1111/ejn.15766
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