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Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation
In Drosophila melanogaster, aversive (electric shock) stimuli have been shown to activate subpopulations of dopaminergic neurons with terminals in the mushroom bodies (MBs) of the brain. While there is compelling evidence that dopamine (DA)-induced synaptic plasticity underpins the formation of aver...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214997/ https://www.ncbi.nlm.nih.gov/pubmed/30389979 http://dx.doi.org/10.1038/s41598-018-34460-1 |
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author | Jarriault, David Fuller, Justine Hyland, Brian I. Mercer, Alison R. |
author_facet | Jarriault, David Fuller, Justine Hyland, Brian I. Mercer, Alison R. |
author_sort | Jarriault, David |
collection | PubMed |
description | In Drosophila melanogaster, aversive (electric shock) stimuli have been shown to activate subpopulations of dopaminergic neurons with terminals in the mushroom bodies (MBs) of the brain. While there is compelling evidence that dopamine (DA)-induced synaptic plasticity underpins the formation of aversive memories in insects, the mechanisms involved have yet to be fully resolved. Here we take advantage of the accessibility of MBs in the brain of the honey bee to examine, using fast scan cyclic voltammetry, the kinetics of DA release and reuptake in vivo in response to electric shock, and to investigate factors that modulate the release of this amine. DA increased transiently in the MBs in response to electric shock stimuli. The magnitude of release varied depending on stimulus duration and intensity, and a strong correlation was identified between DA release and the intensity of behavioural responses to shock. With repeated stimulation, peak DA levels increased. However, the amount of DA released on the first stimulation pulse typically exceeded that evoked by subsequent pulses. No signal was detected in response to odour alone. Interestingly, however, if odour presentation was paired with electric shock, DA release was enhanced. These results set the stage for analysing the mechanisms that modulate DA release in the MBs of the bee. |
format | Online Article Text |
id | pubmed-6214997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-62149972018-11-06 Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation Jarriault, David Fuller, Justine Hyland, Brian I. Mercer, Alison R. Sci Rep Article In Drosophila melanogaster, aversive (electric shock) stimuli have been shown to activate subpopulations of dopaminergic neurons with terminals in the mushroom bodies (MBs) of the brain. While there is compelling evidence that dopamine (DA)-induced synaptic plasticity underpins the formation of aversive memories in insects, the mechanisms involved have yet to be fully resolved. Here we take advantage of the accessibility of MBs in the brain of the honey bee to examine, using fast scan cyclic voltammetry, the kinetics of DA release and reuptake in vivo in response to electric shock, and to investigate factors that modulate the release of this amine. DA increased transiently in the MBs in response to electric shock stimuli. The magnitude of release varied depending on stimulus duration and intensity, and a strong correlation was identified between DA release and the intensity of behavioural responses to shock. With repeated stimulation, peak DA levels increased. However, the amount of DA released on the first stimulation pulse typically exceeded that evoked by subsequent pulses. No signal was detected in response to odour alone. Interestingly, however, if odour presentation was paired with electric shock, DA release was enhanced. These results set the stage for analysing the mechanisms that modulate DA release in the MBs of the bee. Nature Publishing Group UK 2018-11-02 /pmc/articles/PMC6214997/ /pubmed/30389979 http://dx.doi.org/10.1038/s41598-018-34460-1 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jarriault, David Fuller, Justine Hyland, Brian I. Mercer, Alison R. Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title | Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title_full | Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title_fullStr | Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title_full_unstemmed | Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title_short | Dopamine release in mushroom bodies of the honey bee (Apis mellifera L.) in response to aversive stimulation |
title_sort | dopamine release in mushroom bodies of the honey bee (apis mellifera l.) in response to aversive stimulation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6214997/ https://www.ncbi.nlm.nih.gov/pubmed/30389979 http://dx.doi.org/10.1038/s41598-018-34460-1 |
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