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Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle
Sleep is critical for hippocampus-dependent memory consolidation. However, the underlying mechanisms of synaptic plasticity are poorly understood. The central controversy is on whether long-term potentiation (LTP) takes a role during sleep and which would be its specific effect on memory. To address...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447375/ https://www.ncbi.nlm.nih.gov/pubmed/26020963 http://dx.doi.org/10.1371/journal.pcbi.1004241 |
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author | Blanco, Wilfredo Pereira, Catia M. Cota, Vinicius R. Souza, Annie C. Rennó-Costa, César Santos, Sharlene Dias, Gabriella Guerreiro, Ana M. G. Tort, Adriano B. L. Neto, Adrião D. Ribeiro, Sidarta |
author_facet | Blanco, Wilfredo Pereira, Catia M. Cota, Vinicius R. Souza, Annie C. Rennó-Costa, César Santos, Sharlene Dias, Gabriella Guerreiro, Ana M. G. Tort, Adriano B. L. Neto, Adrião D. Ribeiro, Sidarta |
author_sort | Blanco, Wilfredo |
collection | PubMed |
description | Sleep is critical for hippocampus-dependent memory consolidation. However, the underlying mechanisms of synaptic plasticity are poorly understood. The central controversy is on whether long-term potentiation (LTP) takes a role during sleep and which would be its specific effect on memory. To address this question, we used immunohistochemistry to measure phosphorylation of Ca(2+)/calmodulin-dependent protein kinase II (pCaMKIIα) in the rat hippocampus immediately after specific sleep-wake states were interrupted. Control animals not exposed to novel objects during waking (WK) showed stable pCaMKIIα levels across the sleep-wake cycle, but animals exposed to novel objects showed a decrease during subsequent slow-wave sleep (SWS) followed by a rebound during rapid-eye-movement sleep (REM). The levels of pCaMKIIα during REM were proportional to cortical spindles near SWS/REM transitions. Based on these results, we modeled sleep-dependent LTP on a network of fully connected excitatory neurons fed with spikes recorded from the rat hippocampus across WK, SWS and REM. Sleep without LTP orderly rescaled synaptic weights to a narrow range of intermediate values. In contrast, LTP triggered near the SWS/REM transition led to marked swaps in synaptic weight ranking. To better understand the interaction between rescaling and restructuring during sleep, we implemented synaptic homeostasis and embossing in a detailed hippocampal-cortical model with both excitatory and inhibitory neurons. Synaptic homeostasis was implemented by weakening potentiation and strengthening depression, while synaptic embossing was simulated by evoking LTP on selected synapses. We observed that synaptic homeostasis facilitates controlled synaptic restructuring. The results imply a mechanism for a cognitive synergy between SWS and REM, and suggest that LTP at the SWS/REM transition critically influences the effect of sleep: Its lack determines synaptic homeostasis, its presence causes synaptic restructuring. |
format | Online Article Text |
id | pubmed-4447375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-44473752015-06-09 Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle Blanco, Wilfredo Pereira, Catia M. Cota, Vinicius R. Souza, Annie C. Rennó-Costa, César Santos, Sharlene Dias, Gabriella Guerreiro, Ana M. G. Tort, Adriano B. L. Neto, Adrião D. Ribeiro, Sidarta PLoS Comput Biol Research Article Sleep is critical for hippocampus-dependent memory consolidation. However, the underlying mechanisms of synaptic plasticity are poorly understood. The central controversy is on whether long-term potentiation (LTP) takes a role during sleep and which would be its specific effect on memory. To address this question, we used immunohistochemistry to measure phosphorylation of Ca(2+)/calmodulin-dependent protein kinase II (pCaMKIIα) in the rat hippocampus immediately after specific sleep-wake states were interrupted. Control animals not exposed to novel objects during waking (WK) showed stable pCaMKIIα levels across the sleep-wake cycle, but animals exposed to novel objects showed a decrease during subsequent slow-wave sleep (SWS) followed by a rebound during rapid-eye-movement sleep (REM). The levels of pCaMKIIα during REM were proportional to cortical spindles near SWS/REM transitions. Based on these results, we modeled sleep-dependent LTP on a network of fully connected excitatory neurons fed with spikes recorded from the rat hippocampus across WK, SWS and REM. Sleep without LTP orderly rescaled synaptic weights to a narrow range of intermediate values. In contrast, LTP triggered near the SWS/REM transition led to marked swaps in synaptic weight ranking. To better understand the interaction between rescaling and restructuring during sleep, we implemented synaptic homeostasis and embossing in a detailed hippocampal-cortical model with both excitatory and inhibitory neurons. Synaptic homeostasis was implemented by weakening potentiation and strengthening depression, while synaptic embossing was simulated by evoking LTP on selected synapses. We observed that synaptic homeostasis facilitates controlled synaptic restructuring. The results imply a mechanism for a cognitive synergy between SWS and REM, and suggest that LTP at the SWS/REM transition critically influences the effect of sleep: Its lack determines synaptic homeostasis, its presence causes synaptic restructuring. Public Library of Science 2015-05-28 /pmc/articles/PMC4447375/ /pubmed/26020963 http://dx.doi.org/10.1371/journal.pcbi.1004241 Text en © 2015 Blanco et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Blanco, Wilfredo Pereira, Catia M. Cota, Vinicius R. Souza, Annie C. Rennó-Costa, César Santos, Sharlene Dias, Gabriella Guerreiro, Ana M. G. Tort, Adriano B. L. Neto, Adrião D. Ribeiro, Sidarta Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title | Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title_full | Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title_fullStr | Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title_full_unstemmed | Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title_short | Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle |
title_sort | synaptic homeostasis and restructuring across the sleep-wake cycle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4447375/ https://www.ncbi.nlm.nih.gov/pubmed/26020963 http://dx.doi.org/10.1371/journal.pcbi.1004241 |
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