Evidence map›Paper›PMID 24677804›Full record

ArticleDevelopmental neurobiology2015

REM sleep twitches rouse nascent cerebellar circuits: Implications for sensorimotor development.

Greta Sokoloff, Brandt D Uitermarkt, Mark S Blumberg

Abstract read
In one paragraph

Article in Developmental neurobiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Novel Electrophysiological Signatures of Learning and Forgetting in Human Rapid Eye Movement Sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  4. Developmentally Unique Cerebellar Processing Prioritizes Self- over Other-Generated Movements.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Active Sleep Promotes Functional Connectivity in Developing Sensorimotor Networks.BioEssays : news and reviews in molecular, cellular and developmental biology · 2018
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Sensorimotor processing in the newborn rat red nucleus during active sleep.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    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

3 authors at 1 institution in 1 country.

Greta SokoloffDepartment of Psychology, University of Iowa, Iowa City, Iowa.
Brandt D UitermarktDepartment of Psychology, University of Iowa, Iowa City, Iowa.
Mark S BlumbergDepartment of Psychology, University of Iowa, Iowa City, Iowa.
University of Iowa · US

Funding

Behavioral state development in infantsR01HD063071 · NICHD · UNIVERSITY OF IOWA · PI BLUMBERG, MARK SAMUEL · 2010 to 2014
$1.5M
NICHD NIH HHS HD63071NICHD NIH HHS R01 HD063071
6 · The paper itself

Abstract

The cerebellum is critical for sensorimotor integration and undergoes extensive postnatal development. During the first postnatal week in rats, climbing fibers polyinnervate Purkinje cells and, before granule cell migration, mossy fibers make transient, direct connections with Purkinje cells. Activity-dependent processes are assumed to play a critical role in the development and refinement of these and other aspects of cerebellar circuitry. However, the sources and patterning of activity have not been described. We hypothesize that sensory feedback (i.e., reafference) from myoclonic twitches in sleeping newborn rats is a prominent driver of activity for the developing cerebellum. Here, in 6-day-old rats, we show that Purkinje cells exhibit substantial state-dependent changes in complex and simple spike activity-primarily during active sleep. In addition, this activity increases significantly during bouts of twitching. Moreover, the surprising observation of twitch-dependent increases in simple spike activity at this age suggests a functional engagement of mossy fibers before the parallel fiber system has developed. Based on these and other results, we propose that twitching comprises a unique class of self-produced movement that drives critical aspects of activity-dependent development in the cerebellum and other sensorimotor systems.

Indexed as

AnimalsAnimals, NewbornAxonsBehavior, AnimalCerebellumFemaleMaleMotor ActivityMovementNerve NetPurkinje CellsRats, Sprague-DawleySleep, REMcerebellumcorollary dischargemyoclonic twitchingreafferencesleep

Identifiers

PMID24677804
PMCPMC4177987
OpenAlexW1884501296

What OpenQuestion holds

Textmetadata
LicenceTDM
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.