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dc.contributor.authorSantos Ledo, Adrián 
dc.contributor.authorArenzana, F.J.
dc.contributor.authorPorteros Herrero, Ángel Fernando 
dc.contributor.authorLara Pradas, Juan Manuel 
dc.contributor.authorVelasco Arranz, María Almudena 
dc.contributor.authorAijón Noguera, José 
dc.contributor.authorArévalo Arévalo, María Rosario 
dc.date.accessioned2025-01-17T09:46:29Z
dc.date.available2025-01-17T09:46:29Z
dc.date.issued2011
dc.identifier.issn0892-0362
dc.identifier.urihttp://hdl.handle.net/10366/161909
dc.description.abstract[EN]Embryonic exposure to ethanol leads to malformations such as cyclopia. Cyclopic embryos present fused eyes and lack of the ventral specification of the brain, with physiological and morphological defects in the visual system, which provides a useful model for teratology and neurotoxicity assessments. We analysed the differentiation of the visual areas in the ethanol-induced cyclopic animals. For this purpose we exposed zebrafish embryos to 1.5% ethanol from 4 hours post-fertilisation (hpf) to 24 hpf in order to get cyclopic embryos. We monitored cytoarchitecture and quantified both the proliferation rate and cell differentiation from 2 days post-fertilisation (dpf) onwards, focusing on the main components of the visual system (retina, optic nerve and optic tectum) of normal and cyclopic zebrafish embryos. The visual system of the zebrafish embryos is affected by exposure to ethanol; two optic nerves that fuse before leaving the eyes are present in cyclopic specimens but an optic chiasm is not evident. Cell differentiation is severely delayed throughout the visual system at 2 dpf. At 5 dpf, lamination in the cyclopic retina and optic tectum is completed, but they are filled with pyknotic nuclei demonstrating cell death. At this stage the proliferation rate and expression patterns are unaltered and glial and neuronal neurochemical differentiations are similar to untreated animals. We found that the alterations produced by exposure to ethanol are not only cell-selective, but also tissue-selective. Cyclopia is the most severe phenotype induced by ethanol, although cell differentiation and proliferation can reach normal patterns after a certain period of time, which points to a neural plasticity process. Zebrafish embryos may possess a compensation mechanism against the ethanol effect, which would account for their use for pharmacogenetic and chemical screenings in the analysis of new molecules that could improve visual problems.es_ES
dc.description.sponsorshipFunds from the MICINN (BFU2009-11179) and Junta de Castilla y León (Grupo de Excelencia GR-183 and Consejería de Sanidad) supported this work. The authors would like to thank Dr. S Wilson and Dr. F. Cavodeassi for their generous help in the performance of the confocal images at UCL and Miss M.T. Sánchez for her excellent technical assistance. We would also like to thank Mr. G.H. Jenkins for his help with the English version of the manuscript.es_ES
dc.language.isoenges_ES
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectCell proliferationes_ES
dc.subjectDevelopmentes_ES
dc.subjectNeurotoxicityes_ES
dc.subjectRetinal differentitationes_ES
dc.subjectRetinaes_ES
dc.subjectOptic tectumes_ES
dc.subjectZebrafishes_ES
dc.subject.meshMorphogenesis *
dc.subject.meshRetina *
dc.subject.meshDevelopmental Biology *
dc.subject.meshBiochemistry *
dc.subject.meshBiology *
dc.subject.meshZebrafish *
dc.subject.meshCell Biology *
dc.subject.meshVisual Pathways *
dc.titleCytoarchitectonic and neurochemical differentiation of the visual system in ethanol-induced cyclopic zebrafish larvaees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publishversionhttps://doi.org/10.1016/j.ntt.2011.06.001es_ES
dc.subject.unesco2407 Biología Celulares_ES
dc.subject.unesco2302 Bioquímicaes_ES
dc.subject.unesco3206.11 Toxicidad de Los Alimentoses_ES
dc.subject.unesco6113.01 Alcoholismoes_ES
dc.subject.unesco2409.01 Embriologíaes_ES
dc.identifier.doi10.1016/j.ntt.2011.06.001
dc.relation.projectIDBFU2009-11179es_ES
dc.relation.projectIDGR-183es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES
dc.identifier.pmid21684331
dc.journal.titleNeurotoxicology and Teratologyes_ES
dc.volume.number33es_ES
dc.issue.number6es_ES
dc.page.initial686es_ES
dc.page.final697es_ES
dc.type.hasVersioninfo:eu-repo/semantics/publishedVersiones_ES
dc.subject.decsbiología celular *
dc.subject.decsvías visuales *
dc.subject.decsbiología *
dc.subject.decsbioquímica *
dc.subject.decsmorfogénesis *
dc.subject.decspez cebra *
dc.subject.decsbiología del desarrollo *
dc.subject.decsretina *


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