Evidence map›Paper›PMID 31374117›Full record

ArticleSleep2019

Evidence for sleep-dependent synaptic renormalization in mouse pups.

Luisa de Vivo, Hirotaka Nagai, Noemi De Wispelaere, Giovanna Maria Spano, William Marshall, Michele Bellesi, Kelsey Marie Nemec, Shannon Sandra Schiereck, Midori Nagai, Giulio Tononi and 1 more

Abstract read
In one paragraph

Article in Sleep, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
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

21 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. The why and how of sleep-dependent synaptic down-selection.Seminars in cell & developmental biology · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. The Ontogenesis of Mammalian Sleep: Form and Function.Current sleep medicine reports · 2020
    Article
  16. Review
  17. Structural synaptic plasticity across sleep and wake.Current opinion in physiology · 2020
    Review
  18. Review
  19. Effects of sleep and waking on the synaptic ultrastructure.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2020
    Article
  20. 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

11 authors.

Luisa de VivoDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Hirotaka NagaiDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Noemi De WispelaereDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Giovanna Maria SpanoDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
William MarshallDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Michele BellesiDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Kelsey Marie NemecDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Shannon Sandra SchiereckDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Midori NagaiDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Giulio TononiDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.
Chiara CirelliDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI.

Funding

Electron Microscopy Core CP01NS083514 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI TONONI, GIULIO · 2014 to 2018
$7.7M
NINDS NIH HHS P01 NS083514
6 · The paper itself

Abstract

In adolescent and adult brains several molecular, electrophysiological, and ultrastructural measures of synaptic strength are higher after wake than after sleep [1, 2]. These results support the proposal that a core function of sleep is to renormalize the increase in synaptic strength associated with ongoing learning during wake, to reestablish cellular homeostasis and avoid runaway potentiation, synaptic saturation, and memory interference [2, 3]. Before adolescence however, when the brain is still growing and many new synapses are forming, sleep is widely believed to promote synapse formation and growth. To assess the role of sleep on synapses early in life, we studied 2-week-old mouse pups (both sexes) whose brain is still undergoing significant developmental changes, but in which sleep and wake are easy to recognize. In two strains (CD-1, YFP-H) we found that pups spend ~50% of the day asleep and show an immediate increase in total sleep duration after a few hours of enforced wake, indicative of sleep homeostasis. In YFP-H pups we then used serial block-face electron microscopy to examine whether the axon-spine interface (ASI), an ultrastructural marker of synaptic strength, changes between wake and sleep. We found that the ASI of cortical synapses (layer 2, motor cortex) was on average 33.9% smaller after sleep relative to after extended wake and the differences between conditions were consistent with multiplicative scaling. Thus, the need for sleep-dependent synaptic renormalization may apply also to the young, pre-weaned cerebral cortex, at least in the superficial layers of the primary motor area.

Indexed as

AnimalsAnimals, NewbornAxonsCerebral CortexDendritic SpinesElectrophysiological PhenomenaFemaleLearningMaleMiceMicroscopy, ElectronNeuronal PlasticityNeuronsSleepSynapsesWakefulnesscerebral cortexserial electron microscopysleepsynapse

Identifiers

PMID31374117
PMCPMC6802737

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.