Evidence map›Paper›PMID 32015324›Full record

ArticleNPJ schizophrenia2020

Clozapine-induced transcriptional changes in the zebrafish brain.

Joana Viana, Nick Wildman, Eilis Hannon, Audrey Farbos, Paul O' Neill, Karen Moore, Ronny van Aerle, Greg Paull, Eduarda Santos, Jonathan Mill

Open access · goldAbstract read
In one paragraph

Article in NPJ schizophrenia, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 20% 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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
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  6. Review
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

10 authors at 2 institutions in 1 country.

Joana VianaUniversity of Exeter Medical School, University of Exeter, Exeter, UK.
Nick WildmanBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.
Eilis HannonUniversity of Exeter Medical School, University of Exeter, Exeter, UK.
Audrey FarbosBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.
Paul O' NeillBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.
Karen MooreBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0002-0146-0653
Ronny van AerleInternational Centre of Excellence for Aquatic Animal Health, Cefas Weymouth Laboratory, Weymouth, Dorset, UK.ORCID http://orcid.org/0000-0002-2605-6518
Greg PaullBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.
Eduarda SantosBiosciences, College of Life & Environmental Sciences, University of Exeter, Exeter, UK.ORCID http://orcid.org/0000-0002-4074-0121
Jonathan MillUniversity of Exeter Medical School, University of Exeter, Exeter, UK. j.mill@exeter.ac.uk.
University of Exeter · GBCentre for Environment, Fisheries and Aquaculture Science · GB

Funding

RCUK | Medical Research Council (MRC) MR/K013807/1RCUK | Medical Research Council (MRC) MR/M008924/1RCUK | Medical Research Council (MRC) MR/R024987/1
6 · The paper itself

Abstract

Clozapine is an atypical antipsychotic medication that is used to treat schizophrenia patients who are resistant to other antipsychotic drugs. The molecular mechanisms mediating the effects of clozapine are not well understood and its use is often associated with severe side-effects. In this study, we exposed groups of wild-type zebrafish to two doses of clozapine ('low' (20 µg/L) and 'high' (70 µg/L)) over a 72-h period, observing dose-dependent effects on behaviour. Using RNA sequencing (RNA-seq) we identified multiple genes differentially expressed in the zebrafish brain following exposure to clozapine. Network analysis identified co-expression modules characterised by striking changes in module connectivity in response to clozapine, and these were enriched for regulatory pathways relevant to the etiology of schizophrenia. Our study highlights the utility of zebrafish as a model for assessing the molecular consequences of antipsychotic medications and identifies genomic networks potentially involved in schizophrenia.

Identifiers

PMID32015324
PMCPMC6997376
OpenAlexW3003811938

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.