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Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro
Mycotoxins are toxic secondary metabolites formed by various fungal species that are found as natural contaminants in food. This very heterogeneous group of compounds triggers multiple toxic mechanisms, including endocrine disruptive potential. Current risk assessment of mycotoxins, as for most chem...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316405/ https://www.ncbi.nlm.nih.gov/pubmed/27401186 http://dx.doi.org/10.1007/s00204-016-1795-7 |
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author | Vejdovszky, Katharina Hahn, Kathrin Braun, Dominik Warth, Benedikt Marko, Doris |
author_facet | Vejdovszky, Katharina Hahn, Kathrin Braun, Dominik Warth, Benedikt Marko, Doris |
author_sort | Vejdovszky, Katharina |
collection | PubMed |
description | Mycotoxins are toxic secondary metabolites formed by various fungal species that are found as natural contaminants in food. This very heterogeneous group of compounds triggers multiple toxic mechanisms, including endocrine disruptive potential. Current risk assessment of mycotoxins, as for most chemical substances, is based on the effects of single compounds. However, concern on a potential enhancement of risks by interactions of single substances in naturally occurring mixtures has greatly increased recently. In this study, the combinatory effects of three mycoestrogens were investigated in detail. This includes the endocrine disruptors zearalenone (ZEN) and α-zearalenol (α-ZEL) produced by Fusarium fungi and alternariol (AOH), a cytotoxic and estrogenic mycotoxin formed by Alternaria species. For evaluation of effects, estrogen-dependent activation of alkaline phosphatase (AlP) and cell proliferation were tested in the adenocarcinoma cell line Ishikawa. The estrogenic potential varied among the single substances. Half maximum effect concentrations (EC50) for AlP activation were evaluated for α-ZEL, ZEN and AOH as 37 pM, 562 pM and 995 nM, respectively. All three mycotoxins were found to act as partial agonists. The majority of binary combinations, even at very low concentrations in the case of α-ZEL, showed strong synergism in the AlP assay. These potentiating phenomena of mycotoxin mixtures highlight the urgent need to incorporate combinatory effects into future risk assessment, especially when endocrine disruptors are involved. To the best of our knowledge, this study presents the first investigation on synergistic effects of mycoestrogens. |
format | Online Article Text |
id | pubmed-5316405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-53164052017-03-03 Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro Vejdovszky, Katharina Hahn, Kathrin Braun, Dominik Warth, Benedikt Marko, Doris Arch Toxicol Biologics Mycotoxins are toxic secondary metabolites formed by various fungal species that are found as natural contaminants in food. This very heterogeneous group of compounds triggers multiple toxic mechanisms, including endocrine disruptive potential. Current risk assessment of mycotoxins, as for most chemical substances, is based on the effects of single compounds. However, concern on a potential enhancement of risks by interactions of single substances in naturally occurring mixtures has greatly increased recently. In this study, the combinatory effects of three mycoestrogens were investigated in detail. This includes the endocrine disruptors zearalenone (ZEN) and α-zearalenol (α-ZEL) produced by Fusarium fungi and alternariol (AOH), a cytotoxic and estrogenic mycotoxin formed by Alternaria species. For evaluation of effects, estrogen-dependent activation of alkaline phosphatase (AlP) and cell proliferation were tested in the adenocarcinoma cell line Ishikawa. The estrogenic potential varied among the single substances. Half maximum effect concentrations (EC50) for AlP activation were evaluated for α-ZEL, ZEN and AOH as 37 pM, 562 pM and 995 nM, respectively. All three mycotoxins were found to act as partial agonists. The majority of binary combinations, even at very low concentrations in the case of α-ZEL, showed strong synergism in the AlP assay. These potentiating phenomena of mycotoxin mixtures highlight the urgent need to incorporate combinatory effects into future risk assessment, especially when endocrine disruptors are involved. To the best of our knowledge, this study presents the first investigation on synergistic effects of mycoestrogens. Springer Berlin Heidelberg 2016-07-11 2017 /pmc/articles/PMC5316405/ /pubmed/27401186 http://dx.doi.org/10.1007/s00204-016-1795-7 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Biologics Vejdovszky, Katharina Hahn, Kathrin Braun, Dominik Warth, Benedikt Marko, Doris Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title | Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title_full | Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title_fullStr | Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title_full_unstemmed | Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title_short | Synergistic estrogenic effects of Fusarium and Alternaria mycotoxins in vitro |
title_sort | synergistic estrogenic effects of fusarium and alternaria mycotoxins in vitro |
topic | Biologics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5316405/ https://www.ncbi.nlm.nih.gov/pubmed/27401186 http://dx.doi.org/10.1007/s00204-016-1795-7 |
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