Evidence map›Paper›PMID 23772316›Full record

ArticleBrain sciences2013

Sleep patterns and homeostatic mechanisms in adolescent mice.

Aaron B Nelson, Ugo Faraguna, Jeffrey T Zoltan, Giulio Tononi, Chiara Cirelli

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

48 citing papers in PubMed, 80 citations in OpenAlex.

  1. Article
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  4. Article
  5. Developing forebrain synapses are uniquely vulnerable to sleep loss.Proceedings of the National Academy of Sciences of the United States of America · 2024
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  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Shank3 influences mammalian sleep development.Journal of neuroscience research · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Prediction of Locomotor Activity by Infrared Motion Detector on Sleep-wake State in Mice.Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2021
    Article
  18. The Ontogenesis of Mammalian Sleep: Form and Function.Current sleep medicine reports · 2020
    Article
  19. Sleeping Sickness Disrupts the Sleep-Regulating Adenosine System.The Journal of neuroscience : the official journal of the Society for Neuroscience · 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

5 authors at 1 institution in 1 country.

Aaron B NelsonDepartment of Psychiatry, University of Wisconsin-Madison, Madison, WI 53719, USA ; Neuroscience Training Program, University of Wisconsin-Madison, Madison, WI 53706, USA.
Ugo Faraguna
Jeffrey T Zoltan
Giulio Tononi
Chiara Cirelli
University of Wisconsin–Madison · US

Funding

NIH Director's Pioneer Award (RMI)DP1OD000579 · OD · UNIVERSITY OF WISCONSIN-MADISON · PI TONONI, GIULIO · 2005 to 2009
$3.6M
Synapses and Sleep in Neurodevelopment: A Crucial Interaction at a Critical TimeR01MH091326 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI CIRELLI, CHIARA, TONONI, GIULIO · 2010 to 2014
$3.2M
NIH HHS DP1 OD000579NIMH NIH HHS R01 MH091326
6 · The paper itself

Abstract

Sleep changes were studied in mice (n = 59) from early adolescence to adulthood (postnatal days P19-111). REM sleep declined steeply in early adolescence, while total sleep remained constant and NREM sleep increased slightly. Four hours of sleep deprivation starting at light onset were performed from ages P26 through adulthood (>P60). Following this acute sleep deprivation all mice slept longer and with more consolidated sleep bouts, while NREM slow wave activity (SWA) showed high interindividual variability in the younger groups, and increased consistently only after P42. Three parameters together explained up to 67% of the variance in SWA rebound in frontal cortex, including weight-adjusted age and increase in alpha power during sleep deprivation, both of which positively correlated with the SWA response. The third, and strongest predictor was the SWA decline during the light phase in baseline: mice with high peak SWA at light onset, resulting in a large SWA decline, were more likely to show no SWA rebound after sleep deprivation, a result that was also confirmed in parietal cortex. During baseline, however, SWA showed the same homeostatic changes in adolescents and adults, declining in the course of sleep and increasing across periods of spontaneous wake. Thus, we hypothesize that, in young adolescent mice, a ceiling effect and not the immaturity of the cellular mechanisms underlying sleep homeostasis may prevent the SWA rebound when wake is extended beyond its physiological duration.

Indexed as

adolescencecerebral cortexsleep deprivationslow wave activity

Identifiers

PMID23772316
PMCPMC3682503
OpenAlexW2039844429

What OpenQuestion holds

Textmetadata
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.