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Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins

Zearalenone and its metabolites, α-zearalenol and β-zearalenol, demonstrate estradiol-like activity and disrupt physiological functions in animals. This article evaluates the carryover of zearalenone and its selected metabolites from the digesta to intestinal walls (along the entire intestines) in p...

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Autores principales: Zielonka, Łukasz, Waśkiewicz, Agnieszka, Beszterda, Monika, Kostecki, Marian, Dąbrowski, Michał, Obremski, Kazimierz, Goliński, Piotr, Gajęcki, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549746/
https://www.ncbi.nlm.nih.gov/pubmed/26295259
http://dx.doi.org/10.3390/toxins7083210
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author Zielonka, Łukasz
Waśkiewicz, Agnieszka
Beszterda, Monika
Kostecki, Marian
Dąbrowski, Michał
Obremski, Kazimierz
Goliński, Piotr
Gajęcki, Maciej
author_facet Zielonka, Łukasz
Waśkiewicz, Agnieszka
Beszterda, Monika
Kostecki, Marian
Dąbrowski, Michał
Obremski, Kazimierz
Goliński, Piotr
Gajęcki, Maciej
author_sort Zielonka, Łukasz
collection PubMed
description Zearalenone and its metabolites, α-zearalenol and β-zearalenol, demonstrate estradiol-like activity and disrupt physiological functions in animals. This article evaluates the carryover of zearalenone and its selected metabolites from the digesta to intestinal walls (along the entire intestines) in pre-pubertal gilts exposed to low doses of zearalenone over long periods of time. The term “carryover” describes the transfer of mycotoxins from feed to edible tissues, and it was used to assess the risk of mycotoxin exposure for consumers. The experimental gilts with body weight of up to 25 kg were per os administered zearalenone at a daily dose of 40 μg/kg BW (Group E, n = 18) or placebo (Group C, n = 21) over a period of 42 days. In the first weeks of exposure, the highest values of the carryover factor were noted in the duodenum and the jejunum. In animals receiving pure zearalenone, the presence of metabolites was not determined in intestinal tissues. In the last three weeks of the experiment, very high values of the carryover factor were observed in the duodenum and the descending colon. The results of the study indicate that in animals exposed to subclinical doses of zearalenone, the carryover factor could be determined by the distribution and expression of estrogen receptor beta.
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spelling pubmed-45497462015-08-31 Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins Zielonka, Łukasz Waśkiewicz, Agnieszka Beszterda, Monika Kostecki, Marian Dąbrowski, Michał Obremski, Kazimierz Goliński, Piotr Gajęcki, Maciej Toxins (Basel) Article Zearalenone and its metabolites, α-zearalenol and β-zearalenol, demonstrate estradiol-like activity and disrupt physiological functions in animals. This article evaluates the carryover of zearalenone and its selected metabolites from the digesta to intestinal walls (along the entire intestines) in pre-pubertal gilts exposed to low doses of zearalenone over long periods of time. The term “carryover” describes the transfer of mycotoxins from feed to edible tissues, and it was used to assess the risk of mycotoxin exposure for consumers. The experimental gilts with body weight of up to 25 kg were per os administered zearalenone at a daily dose of 40 μg/kg BW (Group E, n = 18) or placebo (Group C, n = 21) over a period of 42 days. In the first weeks of exposure, the highest values of the carryover factor were noted in the duodenum and the jejunum. In animals receiving pure zearalenone, the presence of metabolites was not determined in intestinal tissues. In the last three weeks of the experiment, very high values of the carryover factor were observed in the duodenum and the descending colon. The results of the study indicate that in animals exposed to subclinical doses of zearalenone, the carryover factor could be determined by the distribution and expression of estrogen receptor beta. MDPI 2015-08-18 /pmc/articles/PMC4549746/ /pubmed/26295259 http://dx.doi.org/10.3390/toxins7083210 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zielonka, Łukasz
Waśkiewicz, Agnieszka
Beszterda, Monika
Kostecki, Marian
Dąbrowski, Michał
Obremski, Kazimierz
Goliński, Piotr
Gajęcki, Maciej
Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title_full Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title_fullStr Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title_full_unstemmed Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title_short Zearalenone in the Intestinal Tissues of Immature Gilts Exposed per os to Mycotoxins
title_sort zearalenone in the intestinal tissues of immature gilts exposed per os to mycotoxins
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4549746/
https://www.ncbi.nlm.nih.gov/pubmed/26295259
http://dx.doi.org/10.3390/toxins7083210
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