Evidence map›Paper›PMID 25966356›Full record

ArticlePloS one2015

Sleep Physiology Alterations Precede Plethoric Phenotypic Changes in R6/1 Huntington's Disease Mice.

Fanny Lebreton, Sebastien Cayzac, Susanna Pietropaolo, Yannick Jeantet, Yoon H Cho

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. 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
2.1field-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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Sleep Disorders in Patients with Choreic Syndromes.Current neurology and neuroscience reports · 2023
    Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Orexinergic System in Neurodegenerative Diseases.Frontiers in aging neuroscience · 2021
    Review
  10. Article
  11. Neurophysiological and Behavioral Effects of Anti-Orexinergic Treatments in a Mouse Model of Huntington's Disease.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Article
  12. IKKβ slows Huntington's disease progression in R6/1 mice.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  13. Review
  14. Review
  15. Chronic Paroxetine Treatment Prevents the Emergence of Abnormal Electroencephalogram Oscillations in Huntington's Disease Mice.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2017
    Article
  16. Differential Alteration in Expression of Striatal GABAFrontiers in molecular neuroscience · 2017
    Article
  17. Article
  18. Sustained Gq-Protein Signaling Disrupts Striatal Circuits via JNK.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Article
  19. 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 2 institutions in 1 country.

Fanny LebretonInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France.
Sebastien CayzacInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France.
Susanna PietropaoloInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France.
Yannick JeantetInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France.
Yoon H ChoInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France; Institut de Neurosciences Cognitives et Intégratives d'Aquitaine, CNRS UMR 5287, Bat B2-Avenue des Facultés, 33405 Talence Cedex, France.
Institut de Neurosciences Cognitives et Intégratives d’Aquitaine · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In hereditary neurodegenerative Huntington's disease (HD), there exists a growing consideration that sleep and circadian dysregulations may be important symptoms. It is not known, however, whether sleep abnormalities contribute to other behavioral deficits in HD patients and mouse models. To determine the precise chronology for sleep physiology alterations and other sensory, motor, psychiatric and cognitive symptoms of HD, the same R6/1 HD transgenics and their wild-type littermates were recorded monthly for sleep electroencephalogram (EEG) together with a wide range of behavioral tests according to a longitudinal plan. We found an early and progressive deterioration of both sleep architecture and EEG brain rhythms in R6/1 mice, which are correlated timely with their spatial working memory impairments. Sleep fragmentation and memory impairments were accompanied by the loss of delta (1-4 Hz) power in the transgenic mice, the magnitude of which increased with age and disease progression. These precocious sleep and cognitive impairments were followed by deficits in social behavior, sensory and motor abilities. Our data confirm the existence and importance of sleep physiology alterations in the widely used R6/1 mouse line and highlight their precedence over other plethoric phenotypic changes. The brainwave abnormalities, may represent a novel biomarker and point to innovative therapeutic interventions against HD.

Indexed as

AnimalsBrainCircadian RhythmDisease Models, AnimalDisease ProgressionElectroencephalographyHuntingtin ProteinHuntington DiseaseMaleMiceMotor ActivityNerve Tissue ProteinsNuclear ProteinsSleep DeprivationHtt protein, mouseHuntingtin ProteinNerve Tissue ProteinsNuclear Proteins

Identifiers

PMID25966356
PMCPMC4428700
OpenAlexW2108180838

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.