Evidence map›Paper›PMID 22264613›Full record

ArticleCurrent biology : CB2012

Disrupted circadian rhythms in a mouse model of schizophrenia.

Peter L Oliver, Melanie V Sobczyk, Elizabeth S Maywood, Benjamin Edwards, Sheena Lee, Achilleas Livieratos, Henrik Oster, Rachel Butler, Sofia I H Godinho, Katharina Wulff and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Current biology : CB, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 1 synthesis or guideline pooled it, 95 citations in OpenAlex.

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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

17 authors at 7 institutions in 2 countries.

Peter L OliverMRC Functional Genomics Unit, Department of Physiology, Anatomy and Genetics, University of Oxford, Oxford OX1 3PT, UK.
Melanie V Sobczyk
Elizabeth S Maywood
Benjamin Edwards
Sheena Lee
Achilleas Livieratos
Henrik Oster
Rachel Butler
Sofia I H Godinho
Katharina Wulff
Stuart N Peirson
Simon P Fisher
Johanna E Chesham
Janice W Smith
Michael H Hastings
Kay E Davies
Russell G Foster
University of Oxford · GBJohn Radcliffe Hospital · GBMRC Laboratory of Molecular Biology · GBGenomics (United Kingdom) · GBManor Hospital · GBMax Planck Institute for Biophysical Chemistry · DENuffield Orthopaedic Centre · GB

Funding

Medical Research Council MC_U105170643Medical Research Council MC_U137761449Wellcome Trust 084655
6 · The paper itself

Abstract

Sleep and circadian rhythm disruption has been widely observed in neuropsychiatric disorders including schizophrenia [1] and often precedes related symptoms [2]. However, mechanistic basis for this association remains unknown. Therefore, we investigated the circadian phenotype of blind-drunk (Bdr), a mouse model of synaptosomal-associated protein (Snap)-25 exocytotic disruption that displays schizophrenic endophenotypes modulated by prenatal factors and reversible by antipsychotic treatment [3, 4]. Notably, SNAP-25 has been implicated in schizophrenia from genetic [5-8], pathological [9-13], and functional studies [14-16]. We show here that the rest and activity rhythms of Bdr mice are phase advanced and fragmented under a light/dark cycle, reminiscent of the disturbed sleep patterns observed in schizophrenia. Retinal inputs appear normal in mutants, and clock gene rhythms within the suprachiasmatic nucleus (SCN) are normally phased both in vitro and in vivo. However, the 24 hr rhythms of arginine vasopressin within the SCN and plasma corticosterone are both markedly phase advanced in Bdr mice. We suggest that the Bdr circadian phenotype arises from a disruption of synaptic connectivity within the SCN that alters critical output signals. Collectively, our data provide a link between disruption of circadian activity cycles and synaptic dysfunction in a model of neuropsychiatric disease.

Indexed as

Circadian RhythmMotor ActivityAdultAnimalsArginine VasopressinCorticosteroneDisease Models, AnimalFemaleHumansMaleMiceMicroarray AnalysisMiddle AgedPolymerase Chain ReactionSchizophreniaSleepArginine VasopressinCorticosteroneSnap25 protein, mouseSynaptosomal-Associated Protein 25

Identifiers

PMID22264613
PMCPMC3356578
OpenAlexW2148974618

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.