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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2015
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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. |
format | Online Article Text |
id | pubmed-4549746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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