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Neonicotinoids disrupt memory, circadian behaviour and sleep

Globally, neonicotinoids are the most used insecticides, despite their well-documented sub-lethal effects on beneficial insects. Neonicotinoids are nicotinic acetylcholine receptor agonists. Memory, circadian rhythmicity and sleep are essential for efficient foraging and pollination and require nico...

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Autores principales: Tasman, Kiah, Hidalgo, Sergio, Zhu, Bangfu, Rands, Sean A., Hodge, James J. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820356/
https://www.ncbi.nlm.nih.gov/pubmed/33479461
http://dx.doi.org/10.1038/s41598-021-81548-2
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author Tasman, Kiah
Hidalgo, Sergio
Zhu, Bangfu
Rands, Sean A.
Hodge, James J. L.
author_facet Tasman, Kiah
Hidalgo, Sergio
Zhu, Bangfu
Rands, Sean A.
Hodge, James J. L.
author_sort Tasman, Kiah
collection PubMed
description Globally, neonicotinoids are the most used insecticides, despite their well-documented sub-lethal effects on beneficial insects. Neonicotinoids are nicotinic acetylcholine receptor agonists. Memory, circadian rhythmicity and sleep are essential for efficient foraging and pollination and require nicotinic acetylcholine receptor signalling. The effect of field-relevant concentrations of the European Union-banned neonicotinoids: imidacloprid, clothianidin, thiamethoxam and thiacloprid were tested on Drosophila memory, circadian rhythms and sleep. Field-relevant concentrations of imidacloprid, clothianidin and thiamethoxam disrupted learning, behavioural rhythmicity and sleep whilst thiacloprid exposure only affected sleep. Exposure to imidacloprid and clothianidin prevented the day/night remodelling and accumulation of pigment dispersing factor (PDF) neuropeptide in the dorsal terminals of clock neurons. Knockdown of the neonicotinoid susceptible Dα1 and Dβ2 nicotinic acetylcholine receptor subunits in the mushroom bodies or clock neurons recapitulated the neonicotinoid like deficits in memory or sleep/circadian behaviour respectively. Disruption of learning, circadian rhythmicity and sleep are likely to have far-reaching detrimental effects on beneficial insects in the field.
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spelling pubmed-78203562021-01-22 Neonicotinoids disrupt memory, circadian behaviour and sleep Tasman, Kiah Hidalgo, Sergio Zhu, Bangfu Rands, Sean A. Hodge, James J. L. Sci Rep Article Globally, neonicotinoids are the most used insecticides, despite their well-documented sub-lethal effects on beneficial insects. Neonicotinoids are nicotinic acetylcholine receptor agonists. Memory, circadian rhythmicity and sleep are essential for efficient foraging and pollination and require nicotinic acetylcholine receptor signalling. The effect of field-relevant concentrations of the European Union-banned neonicotinoids: imidacloprid, clothianidin, thiamethoxam and thiacloprid were tested on Drosophila memory, circadian rhythms and sleep. Field-relevant concentrations of imidacloprid, clothianidin and thiamethoxam disrupted learning, behavioural rhythmicity and sleep whilst thiacloprid exposure only affected sleep. Exposure to imidacloprid and clothianidin prevented the day/night remodelling and accumulation of pigment dispersing factor (PDF) neuropeptide in the dorsal terminals of clock neurons. Knockdown of the neonicotinoid susceptible Dα1 and Dβ2 nicotinic acetylcholine receptor subunits in the mushroom bodies or clock neurons recapitulated the neonicotinoid like deficits in memory or sleep/circadian behaviour respectively. Disruption of learning, circadian rhythmicity and sleep are likely to have far-reaching detrimental effects on beneficial insects in the field. Nature Publishing Group UK 2021-01-21 /pmc/articles/PMC7820356/ /pubmed/33479461 http://dx.doi.org/10.1038/s41598-021-81548-2 Text en © The Author(s) 2021 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tasman, Kiah
Hidalgo, Sergio
Zhu, Bangfu
Rands, Sean A.
Hodge, James J. L.
Neonicotinoids disrupt memory, circadian behaviour and sleep
title Neonicotinoids disrupt memory, circadian behaviour and sleep
title_full Neonicotinoids disrupt memory, circadian behaviour and sleep
title_fullStr Neonicotinoids disrupt memory, circadian behaviour and sleep
title_full_unstemmed Neonicotinoids disrupt memory, circadian behaviour and sleep
title_short Neonicotinoids disrupt memory, circadian behaviour and sleep
title_sort neonicotinoids disrupt memory, circadian behaviour and sleep
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7820356/
https://www.ncbi.nlm.nih.gov/pubmed/33479461
http://dx.doi.org/10.1038/s41598-021-81548-2
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