Stability of neocortical synapses across sleep and wake states during the critical period in rats

Sleep is important for brain plasticity, but its exact function remains mysterious. An influential but controversial idea is that a crucial function of sleep is to drive widespread downscaling of excitatory synaptic strengths. Here, we used real-time sleep classification, ex vivo measurements of pos...

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Main Authors: Brian A Cary, Gina G Turrigiano
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-06-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/66304
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spelling doaj-a8904e3f30d742cb90dbba55c3f153482021-07-12T14:39:38ZengeLife Sciences Publications LtdeLife2050-084X2021-06-011010.7554/eLife.66304Stability of neocortical synapses across sleep and wake states during the critical period in ratsBrian A Cary0https://orcid.org/0000-0002-1759-164XGina G Turrigiano1https://orcid.org/0000-0002-4476-4059Department of Biology, Brandeis University, Waltham, United StatesDepartment of Biology, Brandeis University, Waltham, United StatesSleep is important for brain plasticity, but its exact function remains mysterious. An influential but controversial idea is that a crucial function of sleep is to drive widespread downscaling of excitatory synaptic strengths. Here, we used real-time sleep classification, ex vivo measurements of postsynaptic strength, and in vivo optogenetic monitoring of thalamocortical synaptic efficacy to ask whether sleep and wake states can constitutively drive changes in synaptic strength within the neocortex of juvenile rats. We found that miniature excitatory postsynaptic current amplitudes onto L4 and L2/3 pyramidal neurons were stable across sleep- and wake-dense epochs in both primary visual (V1) and prefrontal cortex (PFC). Further, chronic monitoring of thalamocortical synaptic efficacy in V1 of freely behaving animals revealed stable responses across even prolonged periods of natural sleep and wake. Together, these data demonstrate that sleep does not drive widespread downscaling of synaptic strengths during the highly plastic critical period in juvenile animals. Whether this remarkable stability across sleep and wake generalizes to the fully mature nervous system remains to be seen.https://elifesciences.org/articles/66304sleepsynaptic plasticityneocortex
collection DOAJ
language English
format Article
sources DOAJ
author Brian A Cary
Gina G Turrigiano
spellingShingle Brian A Cary
Gina G Turrigiano
Stability of neocortical synapses across sleep and wake states during the critical period in rats
eLife
sleep
synaptic plasticity
neocortex
author_facet Brian A Cary
Gina G Turrigiano
author_sort Brian A Cary
title Stability of neocortical synapses across sleep and wake states during the critical period in rats
title_short Stability of neocortical synapses across sleep and wake states during the critical period in rats
title_full Stability of neocortical synapses across sleep and wake states during the critical period in rats
title_fullStr Stability of neocortical synapses across sleep and wake states during the critical period in rats
title_full_unstemmed Stability of neocortical synapses across sleep and wake states during the critical period in rats
title_sort stability of neocortical synapses across sleep and wake states during the critical period in rats
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-06-01
description Sleep is important for brain plasticity, but its exact function remains mysterious. An influential but controversial idea is that a crucial function of sleep is to drive widespread downscaling of excitatory synaptic strengths. Here, we used real-time sleep classification, ex vivo measurements of postsynaptic strength, and in vivo optogenetic monitoring of thalamocortical synaptic efficacy to ask whether sleep and wake states can constitutively drive changes in synaptic strength within the neocortex of juvenile rats. We found that miniature excitatory postsynaptic current amplitudes onto L4 and L2/3 pyramidal neurons were stable across sleep- and wake-dense epochs in both primary visual (V1) and prefrontal cortex (PFC). Further, chronic monitoring of thalamocortical synaptic efficacy in V1 of freely behaving animals revealed stable responses across even prolonged periods of natural sleep and wake. Together, these data demonstrate that sleep does not drive widespread downscaling of synaptic strengths during the highly plastic critical period in juvenile animals. Whether this remarkable stability across sleep and wake generalizes to the fully mature nervous system remains to be seen.
topic sleep
synaptic plasticity
neocortex
url https://elifesciences.org/articles/66304
work_keys_str_mv AT brianacary stabilityofneocorticalsynapsesacrosssleepandwakestatesduringthecriticalperiodinrats
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