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Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders

Sleep and sleep-like states are present across the animal kingdom, with recent studies convincingly demonstrating sleep-like states in arthropods, nematodes, and even cnidarians. However, the existence of different sleep phases across taxa is as yet unclear. In particular, the study of rapid eye mov...

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Autores principales: Rößler, Daniela C., Kim, Kris, De Agrò, Massimo, Jordan, Alex, Galizia, C Giovanni, Shamble, Paul S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388130/
https://www.ncbi.nlm.nih.gov/pubmed/35939710
http://dx.doi.org/10.1073/pnas.2204754119
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author Rößler, Daniela C.
Kim, Kris
De Agrò, Massimo
Jordan, Alex
Galizia, C Giovanni
Shamble, Paul S.
author_facet Rößler, Daniela C.
Kim, Kris
De Agrò, Massimo
Jordan, Alex
Galizia, C Giovanni
Shamble, Paul S.
author_sort Rößler, Daniela C.
collection PubMed
description Sleep and sleep-like states are present across the animal kingdom, with recent studies convincingly demonstrating sleep-like states in arthropods, nematodes, and even cnidarians. However, the existence of different sleep phases across taxa is as yet unclear. In particular, the study of rapid eye movement (REM) sleep is still largely centered on terrestrial vertebrates, particularly mammals and birds. The most salient indicator of REM sleep is the movement of eyes during this phase. Movable eyes, however, have evolved only in a limited number of lineages—an adaptation notably absent in insects and most terrestrial arthropods—restricting cross-species comparisons. Jumping spiders, however, possess movable retinal tubes to redirect gaze, and in newly emerged spiderlings, these movements can be directly observed through their temporarily translucent exoskeleton. Here, we report evidence for an REM sleep–like state in a terrestrial invertebrate: periodic bouts of retinal movements coupled with limb twitching and stereotyped leg curling behaviors during nocturnal resting in a jumping spider. Observed retinal movement bouts were consistent, including regular durations and intervals, with both increasing over the course of the night. That these characteristic REM sleep–like behaviors exist in a highly visual, long-diverged lineage further challenges our understanding of this sleep state. Comparisons across such long-diverged lineages likely hold important questions and answers about the visual brain as well as the origin, evolution, and function of REM sleep.
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spelling pubmed-93881302022-08-19 Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders Rößler, Daniela C. Kim, Kris De Agrò, Massimo Jordan, Alex Galizia, C Giovanni Shamble, Paul S. Proc Natl Acad Sci U S A Biological Sciences Sleep and sleep-like states are present across the animal kingdom, with recent studies convincingly demonstrating sleep-like states in arthropods, nematodes, and even cnidarians. However, the existence of different sleep phases across taxa is as yet unclear. In particular, the study of rapid eye movement (REM) sleep is still largely centered on terrestrial vertebrates, particularly mammals and birds. The most salient indicator of REM sleep is the movement of eyes during this phase. Movable eyes, however, have evolved only in a limited number of lineages—an adaptation notably absent in insects and most terrestrial arthropods—restricting cross-species comparisons. Jumping spiders, however, possess movable retinal tubes to redirect gaze, and in newly emerged spiderlings, these movements can be directly observed through their temporarily translucent exoskeleton. Here, we report evidence for an REM sleep–like state in a terrestrial invertebrate: periodic bouts of retinal movements coupled with limb twitching and stereotyped leg curling behaviors during nocturnal resting in a jumping spider. Observed retinal movement bouts were consistent, including regular durations and intervals, with both increasing over the course of the night. That these characteristic REM sleep–like behaviors exist in a highly visual, long-diverged lineage further challenges our understanding of this sleep state. Comparisons across such long-diverged lineages likely hold important questions and answers about the visual brain as well as the origin, evolution, and function of REM sleep. National Academy of Sciences 2022-08-08 2022-08-16 /pmc/articles/PMC9388130/ /pubmed/35939710 http://dx.doi.org/10.1073/pnas.2204754119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Biological Sciences
Rößler, Daniela C.
Kim, Kris
De Agrò, Massimo
Jordan, Alex
Galizia, C Giovanni
Shamble, Paul S.
Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title_full Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title_fullStr Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title_full_unstemmed Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title_short Regularly occurring bouts of retinal movements suggest an REM sleep–like state in jumping spiders
title_sort regularly occurring bouts of retinal movements suggest an rem sleep–like state in jumping spiders
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9388130/
https://www.ncbi.nlm.nih.gov/pubmed/35939710
http://dx.doi.org/10.1073/pnas.2204754119
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