Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Vejdovszky, Katharina, Hahn, Kathrin, Braun, Dominik, Warth, Benedikt, Marko, Doris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
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
_version_ 1782508830826954752
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
work_keys_str_mv AT vejdovszkykatharina synergisticestrogeniceffectsoffusariumandalternariamycotoxinsinvitro
AT hahnkathrin synergisticestrogeniceffectsoffusariumandalternariamycotoxinsinvitro
AT braundominik synergisticestrogeniceffectsoffusariumandalternariamycotoxinsinvitro
AT warthbenedikt synergisticestrogeniceffectsoffusariumandalternariamycotoxinsinvitro
AT markodoris synergisticestrogeniceffectsoffusariumandalternariamycotoxinsinvitro