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Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies

Sleep is observed in most animals, which suggests it subserves a fundamental process associated with adaptive biological functions. However, the evidence to directly associate sleep with a specific function is lacking, in part because sleep is not a single process in many animals. In humans and othe...

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Autores principales: Jagannathan, Sridhar R., Jeans, Rhiannon, Van De Poll, Matthew N., van Swinderen, Bruno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312633/
https://www.ncbi.nlm.nih.gov/pubmed/37398087
http://dx.doi.org/10.1101/2023.06.12.544704
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author Jagannathan, Sridhar R.
Jeans, Rhiannon
Van De Poll, Matthew N.
van Swinderen, Bruno
author_facet Jagannathan, Sridhar R.
Jeans, Rhiannon
Van De Poll, Matthew N.
van Swinderen, Bruno
author_sort Jagannathan, Sridhar R.
collection PubMed
description Sleep is observed in most animals, which suggests it subserves a fundamental process associated with adaptive biological functions. However, the evidence to directly associate sleep with a specific function is lacking, in part because sleep is not a single process in many animals. In humans and other mammals, different sleep stages have traditionally been identified using electroencephalograms (EEGs), but such an approach is not feasible in different animals such as insects. Here, we perform long-term multichannel local field potential (LFP) recordings in the brains of behaving flies undergoing spontaneous sleep bouts. We developed protocols to allow for consistent spatial recordings of LFPs across multiple flies, allowing us to compare the LFP activity across awake and sleep periods and further compare the same to induced sleep. Using machine learning, we uncover the existence of distinct temporal stages of sleep and explore the associated spatial and spectral features across the fly brain. Further, we analyze the electrophysiological correlates of micro-behaviours associated with certain sleep stages. We confirm the existence of a distinct sleep stage associated with rhythmic proboscis extensions and show that spectral features of this sleep-related behavior differ significantly from those associated with the same behavior during wakefulness, indicating a dissociation between behavior and the brain states wherein these behaviors reside.
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spelling pubmed-103126332023-07-01 Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies Jagannathan, Sridhar R. Jeans, Rhiannon Van De Poll, Matthew N. van Swinderen, Bruno bioRxiv Article Sleep is observed in most animals, which suggests it subserves a fundamental process associated with adaptive biological functions. However, the evidence to directly associate sleep with a specific function is lacking, in part because sleep is not a single process in many animals. In humans and other mammals, different sleep stages have traditionally been identified using electroencephalograms (EEGs), but such an approach is not feasible in different animals such as insects. Here, we perform long-term multichannel local field potential (LFP) recordings in the brains of behaving flies undergoing spontaneous sleep bouts. We developed protocols to allow for consistent spatial recordings of LFPs across multiple flies, allowing us to compare the LFP activity across awake and sleep periods and further compare the same to induced sleep. Using machine learning, we uncover the existence of distinct temporal stages of sleep and explore the associated spatial and spectral features across the fly brain. Further, we analyze the electrophysiological correlates of micro-behaviours associated with certain sleep stages. We confirm the existence of a distinct sleep stage associated with rhythmic proboscis extensions and show that spectral features of this sleep-related behavior differ significantly from those associated with the same behavior during wakefulness, indicating a dissociation between behavior and the brain states wherein these behaviors reside. Cold Spring Harbor Laboratory 2023-06-13 /pmc/articles/PMC10312633/ /pubmed/37398087 http://dx.doi.org/10.1101/2023.06.12.544704 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use.
spellingShingle Article
Jagannathan, Sridhar R.
Jeans, Rhiannon
Van De Poll, Matthew N.
van Swinderen, Bruno
Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title_full Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title_fullStr Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title_full_unstemmed Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title_short Multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
title_sort multivariate classification of multichannel long-term electrophysiology data identifies different sleep stages in fruit flies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10312633/
https://www.ncbi.nlm.nih.gov/pubmed/37398087
http://dx.doi.org/10.1101/2023.06.12.544704
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