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Refinement of the zebrafish embryo developmental toxicity assay

Several pharmaceutical and chemical companies are using the zebrafish embryo as an alternative to animal testing for early detection of developmental toxicants. Unfortunately, the protocol of this zebrafish embryo assay varies between labs, resulting in discordant data for identical compounds. The a...

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Autores principales: Hoyberghs, Jente, Bars, Chloé, Pype, Casper, Foubert, Kenn, Ayuso Hernando, Miriam, Van Ginneken, Chris, Ball, Jonathan, Van Cruchten, Steven
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588703/
https://www.ncbi.nlm.nih.gov/pubmed/33134094
http://dx.doi.org/10.1016/j.mex.2020.101087
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author Hoyberghs, Jente
Bars, Chloé
Pype, Casper
Foubert, Kenn
Ayuso Hernando, Miriam
Van Ginneken, Chris
Ball, Jonathan
Van Cruchten, Steven
author_facet Hoyberghs, Jente
Bars, Chloé
Pype, Casper
Foubert, Kenn
Ayuso Hernando, Miriam
Van Ginneken, Chris
Ball, Jonathan
Van Cruchten, Steven
author_sort Hoyberghs, Jente
collection PubMed
description Several pharmaceutical and chemical companies are using the zebrafish embryo as an alternative to animal testing for early detection of developmental toxicants. Unfortunately, the protocol of this zebrafish embryo assay varies between labs, resulting in discordant data for identical compounds. The assay also has some limitations, such as low biotransformation capacity and fewer morphological endpoints in comparison with the in vivo mammalian developmental toxicity studies. Consequently, there is a need to standardize and further optimize the assay for developmental toxicity testing. We developed a Zebrafish Embryo Developmental Toxicity Assay (ZEDTA) that can be extended with a metabolic activation system and/or skeletal staining to increase its sensitivity. As such, the ZEDTA can be used as a modular system depending on the compound of interest. • Our protocol is customized with a metabolic activation system for test compounds, using human liver microsomes. This system ensures exposure of zebrafish embryos to metabolites that are relevant for human risk and safety assessment. As human liver microsomes are toxic for the zebrafish embryo, we developed a preincubation system with an ultracentrifugation and subsequent dilution step. • Additionally, we developed a skeletal staining protocol that can be added to the ZEDTA modular system. Our live Alizarin Red staining method detects several bone structures in 5-day old zebrafish larvae in a consistent manner.
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spelling pubmed-75887032020-10-30 Refinement of the zebrafish embryo developmental toxicity assay Hoyberghs, Jente Bars, Chloé Pype, Casper Foubert, Kenn Ayuso Hernando, Miriam Van Ginneken, Chris Ball, Jonathan Van Cruchten, Steven MethodsX Method Article Several pharmaceutical and chemical companies are using the zebrafish embryo as an alternative to animal testing for early detection of developmental toxicants. Unfortunately, the protocol of this zebrafish embryo assay varies between labs, resulting in discordant data for identical compounds. The assay also has some limitations, such as low biotransformation capacity and fewer morphological endpoints in comparison with the in vivo mammalian developmental toxicity studies. Consequently, there is a need to standardize and further optimize the assay for developmental toxicity testing. We developed a Zebrafish Embryo Developmental Toxicity Assay (ZEDTA) that can be extended with a metabolic activation system and/or skeletal staining to increase its sensitivity. As such, the ZEDTA can be used as a modular system depending on the compound of interest. • Our protocol is customized with a metabolic activation system for test compounds, using human liver microsomes. This system ensures exposure of zebrafish embryos to metabolites that are relevant for human risk and safety assessment. As human liver microsomes are toxic for the zebrafish embryo, we developed a preincubation system with an ultracentrifugation and subsequent dilution step. • Additionally, we developed a skeletal staining protocol that can be added to the ZEDTA modular system. Our live Alizarin Red staining method detects several bone structures in 5-day old zebrafish larvae in a consistent manner. Elsevier 2020-10-07 /pmc/articles/PMC7588703/ /pubmed/33134094 http://dx.doi.org/10.1016/j.mex.2020.101087 Text en © 2020 The Author(s). Published by Elsevier B.V. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Method Article
Hoyberghs, Jente
Bars, Chloé
Pype, Casper
Foubert, Kenn
Ayuso Hernando, Miriam
Van Ginneken, Chris
Ball, Jonathan
Van Cruchten, Steven
Refinement of the zebrafish embryo developmental toxicity assay
title Refinement of the zebrafish embryo developmental toxicity assay
title_full Refinement of the zebrafish embryo developmental toxicity assay
title_fullStr Refinement of the zebrafish embryo developmental toxicity assay
title_full_unstemmed Refinement of the zebrafish embryo developmental toxicity assay
title_short Refinement of the zebrafish embryo developmental toxicity assay
title_sort refinement of the zebrafish embryo developmental toxicity assay
topic Method Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7588703/
https://www.ncbi.nlm.nih.gov/pubmed/33134094
http://dx.doi.org/10.1016/j.mex.2020.101087
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