Evidence map›Paper›PMID 32248786›Full record

ReviewPhilosophical transactions of the Royal Society of London. Series B, Biological sciences2020

Experience and sleep-dependent synaptic plasticity: from structure to activity.

Linlin Sun, Hang Zhou, Joseph Cichon, Guang Yang

Open access · greenAbstract readReview
In one paragraph

Review in Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 32 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Critical periods and Autism Spectrum Disorders, a role for sleep.Neurobiology of sleep and circadian rhythms · 2023
    Article
  14. A model of autonomous interactions between hippocampus and neocortex driving sleep-dependent memory consolidation.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  15. Article
  16. The role of calcium and CaMKII in sleep.Frontiers in systems neuroscience · 2022
    Review
  17. Review
  18. Article
  19. Article
  20. Memories replayed: reactivating past successes and new dilemmas.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
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

4 authors at 2 institutions in 1 country.

Linlin SunDepartment of Anesthesiology, Columbia University, New York, NY, USA.
Hang ZhouDepartment of Anesthesiology, Columbia University, New York, NY, USA.
Joseph CichonDepartment of Anesthesiology and Critical Care, University of Pennsylvania, Philadelphia, PA, USA.
Guang YangDepartment of Anesthesiology, Columbia University, New York, NY, USA.
Columbia University · USUniversity of Pennsylvania · US

Funding

The roles of anesthetics and neuroimmune interactions in postoperative cognitive dysfunctionR35GM131765 · NIGMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Guang Yang · 2019 to 2026
$3.4M
The role of neuroimmune interactions in the pathogenesis of chronic painR01AA027108 · NIAAA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI CHAO, MOSES VICTOR, YANG, GUANG · 2018 to 2022
$2.9M
NIAAA NIH HHS R01 AA027108NIGMS NIH HHS R35 GM131765
6 · The paper itself

Abstract

Synaptic plasticity is important for learning and memory. With increasing evidence linking sleep states to changes in synaptic strength, an emerging view is that sleep promotes learning and memory by facilitating experience-induced synaptic plasticity. In this review, we summarize the recent progress on the function of sleep in regulating cortical synaptic plasticity. Specifically, we outline the electroencephalogram signatures of sleep states (e.g. slow-wave sleep, rapid eye movement sleep, spindles), sleep state-dependent changes in gene and synaptic protein expression, synaptic morphology, and neuronal and network activity. We highlight studies showing that post-experience sleep potentiates experience-induced synaptic changes and discuss the potential mechanisms that may link sleep-related brain activity to synaptic structural remodelling. We conclude that both synapse formation or strengthening and elimination or weakening occur across sleep. This sleep-dependent synaptic plasticity plays an important role in neuronal circuit refinement during development and after learning, while sleep disorders may contribute to or exacerbate the development of common neurological diseases. This article is part of the Theo Murphy meeting issue 'Memory reactivation: replaying events past, present and future'.

Indexed as

AnimalsGene ExpressionHumansLearningMemory ConsolidationMiceNeuronal PlasticityNeuronsRatsSleepdendritic calcium spikedendritic spinerapid eye movement sleepreplayslow-wave sleepsynaptic plasticity

Identifiers

PMID32248786
PMCPMC7209921
OpenAlexW3014749534

What OpenQuestion holds

Textmetadata
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.