Evidence map›Paper›PMID 25383948›Full record

ArticlePloS one2014

Transient exposure to ethanol during zebrafish embryogenesis results in defects in neuronal differentiation: an alternative model system to study FASD.

Xavier Joya, Oscar Garcia-Algar, Oriol Vall, Cristina Pujades

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. 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
6.6field-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

21 citing papers in PubMed, 40 citations in OpenAlex.

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  6. Zebrafish models of fetal alcohol spectrum disorders.Genesis (New York, N.Y. : 2000) · 2021
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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

4 authors at 4 institutions in 1 country.

Xavier JoyaUnitat de Recerca Infància i Entorn (URIE), Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; Red de Salud Materno-Infantil y del Desarrollo (SAMID), Programa RETICS, Instituto Carlos III, Madrid, Spain.
Oscar Garcia-AlgarUnitat de Recerca Infància i Entorn (URIE), Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; Red de Salud Materno-Infantil y del Desarrollo (SAMID), Programa RETICS, Instituto Carlos III, Madrid, Spain; Departament de Pediatria, Ginecologia i Obstetricia i de Medicina Preventiva, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain.
Oriol VallUnitat de Recerca Infància i Entorn (URIE), Institut Hospital del Mar d'Investigacions Mèdiques, Barcelona, Spain; Red de Salud Materno-Infantil y del Desarrollo (SAMID), Programa RETICS, Instituto Carlos III, Madrid, Spain; Departament de Pediatria, Ginecologia i Obstetricia i de Medicina Preventiva, Universitat Autònoma de Barcelona (UAB), Bellaterra, Spain.
Cristina PujadesDepartment of Experimental and Health Sciences, Universitat Pompeu Fabra (UPF), Parc de Recerca Biomedica de Barcelona, Barcelona, Spain.
Hospital del Mar Research Institute · ESInstituto de Salud Carlos III · ESPompeu Fabra University · ESUniversitat Autònoma de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe exposure of the human embryo to ethanol results in a spectrum of disorders involving multiple organ systems, including the impairment of the development of the central nervous system (CNS). In spite of the importance for human health, the molecular basis of prenatal ethanol exposure remains poorly understood, mainly to the difficulty of sample collection. Zebrafish is now emerging as a powerful organism for the modeling and the study of human diseases. In this work, we have assessed the sensitivity of specific subsets of neurons to ethanol exposure during embryogenesis and we have visualized the sensitive embryonic developmental periods for specific neuronal groups by the use of different transgenic zebrafish lines. METHODOLOGY/PRINCIPAL

findingsIn order to evaluate the teratogenic effects of acute ethanol exposure, we exposed zebrafish embryos to ethanol in a given time window and analyzed the effects in neurogenesis, neuronal differentiation and brain patterning. Zebrafish larvae exposed to ethanol displayed small eyes and/or a reduction of the body length, phenotypical features similar to the observed in children with prenatal exposure to ethanol. When neuronal populations were analyzed, we observed a clear reduction in the number of differentiated neurons in the spinal cord upon ethanol exposure. There was a decrease in the population of sensory neurons mainly due to a decrease in cell proliferation and subsequent apoptosis during neuronal differentiation, with no effect in motoneuron specification.

conclusionOur investigation highlights that transient exposure to ethanol during early embryonic development affects neuronal differentiation although does not result in defects in early neurogenesis. These results establish the use of zebrafish embryos as an alternative research model to elucidate the molecular mechanism(s) of ethanol-induced developmental toxicity at very early stages of embryonic development.

Indexed as

AnimalsBody PatterningCell DifferentiationDisease Models, AnimalEmbryonic DevelopmentEmbryo, NonmammalianEthanolFetal Alcohol Spectrum DisordersGene Expression Regulation, DevelopmentalHumansNeurogenesisNeuronsZebrafishEthanol

Identifiers

PMID25383948
PMCPMC4226617
OpenAlexW2040017882

What OpenQuestion holds

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LicenceCC BY
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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.