Evidence map›Paper›PMID 26843602›Full record

ArticleJournal of neurophysiology2016

Synaptic refinement during development and its effect on slow-wave activity: a computational study.

Erik P Hoel, Larissa Albantakis, Chiara Cirelli, Giulio Tononi

Abstract read
In one paragraph

Article in Journal of neurophysiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Sleep Disorders across the Lifespan: A Different Perspective.International journal of environmental research and public health · 2020
    Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Local aspects of sleep and wakefulness.Current opinion in neurobiology · 2017
    Review
  14. Sleep Loss Promotes Astrocytic Phagocytosis and Microglial Activation in Mouse Cerebral Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  15. 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.

Erik P HoelDepartment of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin; and Neuroscience Training Program, University of Wisconsin-Madison, Madison, Wisconsin.
Larissa AlbantakisDepartment of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin; and.
Chiara CirelliDepartment of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin; and.
Giulio TononiDepartment of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin; and gtononi@wisc.edu.

Funding

NEUROSCIENCE TRAINING PROGRAMT32GM007507 · NIGMS · UNIVERSITY OF WISCONSIN-MADISON · PI HALLORAN, MARY C · 1985 to 2017
$9.3M
Electron Microscopy Core CP01NS083514 · NINDS · UNIVERSITY OF WISCONSIN-MADISON · PI CIRELLI, CHIARA · 2014 to 2018
$7.7M
The cost of plasticity: from cells to systemsR01MH099231 · NIMH · UNIVERSITY OF WISCONSIN-MADISON · PI CIRELLI, CHIARA, TONONI, GIULIO · 2013 to 2017
$3.3M
NIGMS NIH HHS T32 GM007507NIMH NIH HHS R01MH099231NINDS NIH HHS P01NS083514
6 · The paper itself

Abstract

Recent evidence suggests that synaptic refinement, the reorganization of synapses and connections without significant change in their number or strength, is important for the development of the visual system of juvenile rodents. Other evidence in rodents and humans shows that there is a marked drop in sleep slow-wave activity (SWA) during adolescence. Slow waves reflect synchronous transitions of neuronal populations between active and inactive states, and the amount of SWA is influenced by the connection strength and organization of cortical neurons. In this study, we investigated whether synaptic refinement could account for the observed developmental drop in SWA. To this end, we employed a large-scale neural model of primary visual cortex and sections of the thalamus, capable of producing realistic slow waves. In this model, we reorganized intralaminar connections according to experimental data on synaptic refinement: during prerefinement, local connections between neurons were homogenous, whereas in postrefinement, neurons connected preferentially to neurons with similar receptive fields and preferred orientations. Synaptic refinement led to a drop in SWA and to changes in slow-wave morphology, consistent with experimental data. To test whether learning can induce synaptic refinement, intralaminar connections were equipped with spike timing-dependent plasticity. Oriented stimuli were presented during a learning period, followed by homeostatic synaptic renormalization. This led to activity-dependent refinement accompanied again by a decline in SWA. Together, these modeling results show that synaptic refinement can account for developmental changes in SWA. Thus sleep SWA may be used to track noninvasively the reorganization of cortical connections during development.

Indexed as

Brain WavesModels, NeurologicalSleepSynaptic PotentialsAnimalsHumansNeurogenesisNeuronsThalamusVisual Cortexcortical organizationsleepvisual cortex

Identifiers

PMID26843602
PMCPMC4869496

What OpenQuestion holds

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Registered trials

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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.