Evidence map›Paper›PMID 26020963›Full record

ArticlePLoS computational biology2015

Synaptic Homeostasis and Restructuring across the Sleep-Wake Cycle.

Wilfredo Blanco, Catia M Pereira, Vinicius R Cota, Annie C Souza, César Rennó-Costa, Sharlene Santos, Gabriella Dias, Ana M G Guerreiro, Adriano B L Tort, Adrião D Neto and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.1field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  3. The use ofFrontiers in cell and developmental biology · 2026
    Review
  4. Differential expression of spatiotemporal sleep spindle clusters in aging.Sleep advances : a journal of the Sleep Research Society · 2025
    Article
  5. Article
  6. Increased relative abundance ofFrontiers in sleep · 2025
    Article
  7. Article
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  9. Article
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  12. A mechanism for learning with sleep spindles.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Review
  13. Article
  14. Article
  15. Review
  16. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Wilfredo BlancoBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil; Department of Computer and Automation, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil; Department of Computer Science, State University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Catia M PereiraEdmond and Lily Safra International Institute of Neuroscience of Natal (ELS-IINN), Natal, Rio Grande do Norte, Brazil.
Vinicius R CotaBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil; Laboratory of Neuroengineerging and Neuroscience, Federal University of São João Del-Rei, São João Del-Rei, Minas Gerais, Brazil.
Annie C SouzaBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
César Rennó-CostaBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Sharlene SantosBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Gabriella DiasBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Ana M G GuerreiroDepartment of Biomedical Engineering, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Adriano B L TortBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Adrião D NetoDepartment of Computer and Automation, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Sidarta RibeiroBrain Institute, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
Universidade Federal do Rio Grande do Norte · BRFederal University of São João del-Rei · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 Ca2+/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.

Indexed as

Models, NeurologicalAction PotentialsAnimalsCalcium-Calmodulin-Dependent Protein Kinase Type 2Electrophysiological PhenomenaHippocampusHomeostasisLong-Term PotentiationMaleMemory ConsolidationModels, PsychologicalNeuronal PlasticityRatsRats, WistarSleepSleep, REMCalcium-Calmodulin-Dependent Protein Kinase Type 2

Identifiers

PMID26020963
PMCPMC4447375
OpenAlexW2108605189

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.