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Hepatotoxic combination effects of three azole fungicides in a broad dose range
Single active substances of pesticides are thoroughly examined for their toxicity before approval. In this context, the liver is frequently found to be the main target organ. Since consumers are generally exposed to multiple residues of different active substances via the diet, it is important to an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818588/ https://www.ncbi.nlm.nih.gov/pubmed/29038839 http://dx.doi.org/10.1007/s00204-017-2087-6 |
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author | Heise, T. Schmidt, F. Knebel, C. Rieke, S. Haider, W. Geburek, I. Niemann, L. Marx-Stoelting, P. |
author_facet | Heise, T. Schmidt, F. Knebel, C. Rieke, S. Haider, W. Geburek, I. Niemann, L. Marx-Stoelting, P. |
author_sort | Heise, T. |
collection | PubMed |
description | Single active substances of pesticides are thoroughly examined for their toxicity before approval. In this context, the liver is frequently found to be the main target organ. Since consumers are generally exposed to multiple residues of different active substances via the diet, it is important to analyse combinations of active substances for potential mixture effects. For the (tri-)azoles, a group of agricultural fungicides and antifungal drugs, combination effects on the liver are likely because of a similar mode of action. Hepatotoxic effects of mixtures of two triazoles (cyproconazole and epoxiconazole) and an imidazole (prochloraz) were investigated in a 28-day feeding study in rats at three dose levels ranging from a typical toxicological reference value to a clear effect dose. Test parameters included organ weights, clinical chemistry, histopathology and morphometry. In addition, molecular parameters were investigated by means of pathway-focused gene expression arrays, quantitative real-time PCR and enzyme activity assays. Effects were compared to those caused by the individual substances as observed at the same dose levels in a previous study. Mixture effects were substantiated by increases in relative and absolute liver weights, histopathological findings and alterations in clinical chemistry parameters at the top dose level. On the molecular level also at lower dose levels, additive effects could be observed for the induction of several cytochrome P 450 enzymes (Cyp1a1, Cyp2b1, Cyp3a2), transporters (Abcb1a, Abcc3) and of genes encoding for enzymes involved in fatty acid or phospholipid metabolism (Ppargc1a, Sc4 mol). In most cases, treatment with mixtures caused a more pronounced effect as compared to the individual substances. However, the assumption of dose additivity was in general sufficiently conservative to cover mixture effects observed under the conditions of the present study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-017-2087-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5818588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-58185882018-02-27 Hepatotoxic combination effects of three azole fungicides in a broad dose range Heise, T. Schmidt, F. Knebel, C. Rieke, S. Haider, W. Geburek, I. Niemann, L. Marx-Stoelting, P. Arch Toxicol Organ Toxicity and Mechanisms Single active substances of pesticides are thoroughly examined for their toxicity before approval. In this context, the liver is frequently found to be the main target organ. Since consumers are generally exposed to multiple residues of different active substances via the diet, it is important to analyse combinations of active substances for potential mixture effects. For the (tri-)azoles, a group of agricultural fungicides and antifungal drugs, combination effects on the liver are likely because of a similar mode of action. Hepatotoxic effects of mixtures of two triazoles (cyproconazole and epoxiconazole) and an imidazole (prochloraz) were investigated in a 28-day feeding study in rats at three dose levels ranging from a typical toxicological reference value to a clear effect dose. Test parameters included organ weights, clinical chemistry, histopathology and morphometry. In addition, molecular parameters were investigated by means of pathway-focused gene expression arrays, quantitative real-time PCR and enzyme activity assays. Effects were compared to those caused by the individual substances as observed at the same dose levels in a previous study. Mixture effects were substantiated by increases in relative and absolute liver weights, histopathological findings and alterations in clinical chemistry parameters at the top dose level. On the molecular level also at lower dose levels, additive effects could be observed for the induction of several cytochrome P 450 enzymes (Cyp1a1, Cyp2b1, Cyp3a2), transporters (Abcb1a, Abcc3) and of genes encoding for enzymes involved in fatty acid or phospholipid metabolism (Ppargc1a, Sc4 mol). In most cases, treatment with mixtures caused a more pronounced effect as compared to the individual substances. However, the assumption of dose additivity was in general sufficiently conservative to cover mixture effects observed under the conditions of the present study. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00204-017-2087-6) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2017-10-16 2018 /pmc/articles/PMC5818588/ /pubmed/29038839 http://dx.doi.org/10.1007/s00204-017-2087-6 Text en © The Author(s) 2017 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 | Organ Toxicity and Mechanisms Heise, T. Schmidt, F. Knebel, C. Rieke, S. Haider, W. Geburek, I. Niemann, L. Marx-Stoelting, P. Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title | Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title_full | Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title_fullStr | Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title_full_unstemmed | Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title_short | Hepatotoxic combination effects of three azole fungicides in a broad dose range |
title_sort | hepatotoxic combination effects of three azole fungicides in a broad dose range |
topic | Organ Toxicity and Mechanisms |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818588/ https://www.ncbi.nlm.nih.gov/pubmed/29038839 http://dx.doi.org/10.1007/s00204-017-2087-6 |
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