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Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos
Silver is a non-essential, toxic metal widespread in freshwaters and capable of causing adverse effects to wildlife. Its toxic effects have been studied in detail but less is known about how sensitivity varies during development and whether pre-exposures affect tolerance upon re-exposure. We address...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609441/ https://www.ncbi.nlm.nih.gov/pubmed/33083906 http://dx.doi.org/10.1007/s00418-020-01933-2 |
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author | Robinson, Paige C. Littler, Hannah R. Lange, Anke Santos, Eduarda M. |
author_facet | Robinson, Paige C. Littler, Hannah R. Lange, Anke Santos, Eduarda M. |
author_sort | Robinson, Paige C. |
collection | PubMed |
description | Silver is a non-essential, toxic metal widespread in freshwaters and capable of causing adverse effects to wildlife. Its toxic effects have been studied in detail but less is known about how sensitivity varies during development and whether pre-exposures affect tolerance upon re-exposure. We address these knowledge gaps using the zebrafish embryo (Danio rerio) model to investigate whether exposures encompassing stages of development prior to mid-blastula transition, when chorion hardening and epigenetic reprogramming occur, result in greater toxicity compared to those initiated after this period. We conducted exposures to silver initiated at 0.5 h post fertilisation (hpf) and 4 hpf to determine if toxicity differed. In parallel, we exposed embryos to the methylation inhibitor 5-azacytidine as a positive control. Toxicity increased when exposures started from 0.5 hpf compared to 4 hpf and LC50 were significantly lower by 1.2 and 7.6 times for silver and 5-azacyitidine, respectively. We then investigated whether pre-exposure to silver during early development (from 0.5 or 4 hpf) affected the outcome of subsequent exposures during the larvae stage, and found no alterations in toxicity compared to naïve larvae. Together, these data demonstrate that during early development zebrafish embryos are more sensitive to silver when experiments are initiated at the one-cell stage, but that pre-exposures do not influence the outcome of subsequent exposures, suggesting that no long-lasting memory capable of influencing future susceptibility was maintained under our experimental conditions. The finding that toxicity is greater for exposures initiated at the one-cell stage has implications for designing testing systems to assess chemical toxicity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00418-020-01933-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7609441 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-76094412020-11-10 Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos Robinson, Paige C. Littler, Hannah R. Lange, Anke Santos, Eduarda M. Histochem Cell Biol Original Paper Silver is a non-essential, toxic metal widespread in freshwaters and capable of causing adverse effects to wildlife. Its toxic effects have been studied in detail but less is known about how sensitivity varies during development and whether pre-exposures affect tolerance upon re-exposure. We address these knowledge gaps using the zebrafish embryo (Danio rerio) model to investigate whether exposures encompassing stages of development prior to mid-blastula transition, when chorion hardening and epigenetic reprogramming occur, result in greater toxicity compared to those initiated after this period. We conducted exposures to silver initiated at 0.5 h post fertilisation (hpf) and 4 hpf to determine if toxicity differed. In parallel, we exposed embryos to the methylation inhibitor 5-azacytidine as a positive control. Toxicity increased when exposures started from 0.5 hpf compared to 4 hpf and LC50 were significantly lower by 1.2 and 7.6 times for silver and 5-azacyitidine, respectively. We then investigated whether pre-exposure to silver during early development (from 0.5 or 4 hpf) affected the outcome of subsequent exposures during the larvae stage, and found no alterations in toxicity compared to naïve larvae. Together, these data demonstrate that during early development zebrafish embryos are more sensitive to silver when experiments are initiated at the one-cell stage, but that pre-exposures do not influence the outcome of subsequent exposures, suggesting that no long-lasting memory capable of influencing future susceptibility was maintained under our experimental conditions. The finding that toxicity is greater for exposures initiated at the one-cell stage has implications for designing testing systems to assess chemical toxicity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00418-020-01933-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-10-21 2020 /pmc/articles/PMC7609441/ /pubmed/33083906 http://dx.doi.org/10.1007/s00418-020-01933-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Original Paper Robinson, Paige C. Littler, Hannah R. Lange, Anke Santos, Eduarda M. Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title | Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title_full | Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title_fullStr | Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title_full_unstemmed | Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title_short | Developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
title_sort | developmental exposure window influences silver toxicity but does not affect the susceptibility to subsequent exposures in zebrafish embryos |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7609441/ https://www.ncbi.nlm.nih.gov/pubmed/33083906 http://dx.doi.org/10.1007/s00418-020-01933-2 |
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