Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes

Abstract Decades after being banned in many countries, DDT and its metabolites are still considered major environmental hazards. The p,p′‐DDE isomer, the DDT metabolite found in highest concentration in aquaculture feeds, is an endocrine disruptor with demonstrated ability to induce epigenetic effec...

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Published in:Journal of Applied Toxicology
Main Authors: Olsvik, Pål A., Søfteland, Liv
Other Authors: Norges Forskningsråd
Format: Article in Journal/Newspaper
Language:English
Published: Wiley 2017
Subjects:
Online Access:http://dx.doi.org/10.1002/jat.3556
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spelling crwiley:10.1002/jat.3556 2024-06-02T08:03:30+00:00 Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes Olsvik, Pål A. Søfteland, Liv Norges Forskningsråd 2017 http://dx.doi.org/10.1002/jat.3556 https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjat.3556 https://onlinelibrary.wiley.com/doi/full/10.1002/jat.3556 en eng Wiley http://onlinelibrary.wiley.com/termsAndConditions#vor Journal of Applied Toxicology volume 38, issue 4, page 489-503 ISSN 0260-437X 1099-1263 journal-article 2017 crwiley https://doi.org/10.1002/jat.3556 2024-05-03T11:50:06Z Abstract Decades after being banned in many countries, DDT and its metabolites are still considered major environmental hazards. The p,p′‐DDE isomer, the DDT metabolite found in highest concentration in aquaculture feeds, is an endocrine disruptor with demonstrated ability to induce epigenetic effects. This study aimed at examining the impact of p,p′‐DDE on Atlantic salmon. Primary hepatocytes were exposed to four concentrations of p,p′‐DDE (0.1, 1, 10, 100 μ m ) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μ m ). p,p′‐DDE was moderately cytotoxic at 100 μ m . No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μ m p,p′‐DDE, while ar showed strongest response at 100 μ m . Metabolomics profiling showed that p,p′‐DDE at 100 μ m most strongly affected carbohydrate metabolism, primary bile acid metabolism, leucine, isoleucine and valine metabolism, diacylglycerol and sphingolipid metabolism. Observed changes in lipid levels suggest that p,p′‐DDE interferes with phospholipid membrane biosynthesis. Elevation of bile acid levels in p,p′‐DDE‐exposed hepatocytes indicates upregulation of synthesis of bile acids after cytochrome P450 activation. Pathway analysis showed that the superpathway of methionine degradation was the most significantly affected pathway by p,p′‐DDE exposure, while endocrine system disorder topped the diseases and disorder ranking. In conclusion, this work predicts an endocrine response to p,p′‐DDE exposure, and demonstrates how this legacy pesticide might interfere with mechanisms linked to DNA methylation in Atlantic salmon hepatocytes. Article in Journal/Newspaper Atlantic salmon Wiley Online Library Journal of Applied Toxicology 38 4 489 503
institution Open Polar
collection Wiley Online Library
op_collection_id crwiley
language English
description Abstract Decades after being banned in many countries, DDT and its metabolites are still considered major environmental hazards. The p,p′‐DDE isomer, the DDT metabolite found in highest concentration in aquaculture feeds, is an endocrine disruptor with demonstrated ability to induce epigenetic effects. This study aimed at examining the impact of p,p′‐DDE on Atlantic salmon. Primary hepatocytes were exposed to four concentrations of p,p′‐DDE (0.1, 1, 10, 100 μ m ) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μ m ). p,p′‐DDE was moderately cytotoxic at 100 μ m . No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μ m p,p′‐DDE, while ar showed strongest response at 100 μ m . Metabolomics profiling showed that p,p′‐DDE at 100 μ m most strongly affected carbohydrate metabolism, primary bile acid metabolism, leucine, isoleucine and valine metabolism, diacylglycerol and sphingolipid metabolism. Observed changes in lipid levels suggest that p,p′‐DDE interferes with phospholipid membrane biosynthesis. Elevation of bile acid levels in p,p′‐DDE‐exposed hepatocytes indicates upregulation of synthesis of bile acids after cytochrome P450 activation. Pathway analysis showed that the superpathway of methionine degradation was the most significantly affected pathway by p,p′‐DDE exposure, while endocrine system disorder topped the diseases and disorder ranking. In conclusion, this work predicts an endocrine response to p,p′‐DDE exposure, and demonstrates how this legacy pesticide might interfere with mechanisms linked to DNA methylation in Atlantic salmon hepatocytes.
author2 Norges Forskningsråd
format Article in Journal/Newspaper
author Olsvik, Pål A.
Søfteland, Liv
spellingShingle Olsvik, Pål A.
Søfteland, Liv
Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
author_facet Olsvik, Pål A.
Søfteland, Liv
author_sort Olsvik, Pål A.
title Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
title_short Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
title_full Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
title_fullStr Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
title_full_unstemmed Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
title_sort metabolic effects of p,p′‐dde on atlantic salmon hepatocytes
publisher Wiley
publishDate 2017
url http://dx.doi.org/10.1002/jat.3556
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fjat.3556
https://onlinelibrary.wiley.com/doi/full/10.1002/jat.3556
genre Atlantic salmon
genre_facet Atlantic salmon
op_source Journal of Applied Toxicology
volume 38, issue 4, page 489-503
ISSN 0260-437X 1099-1263
op_rights http://onlinelibrary.wiley.com/termsAndConditions#vor
op_doi https://doi.org/10.1002/jat.3556
container_title Journal of Applied Toxicology
container_volume 38
container_issue 4
container_start_page 489
op_container_end_page 503
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