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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Online Access: | https://elifesciences.org/articles/66304 |
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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 AT ginagturrigiano stabilityofneocorticalsynapsesacrosssleepandwakestatesduringthecriticalperiodinrats |
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