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

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...

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Veröffentlicht in:Journal of applied toxicology 2018-04, Vol.38 (4), p.489-503
Hauptverfasser: Olsvik, Pål A., Søfteland, Liv
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description 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 μm) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μm). p,p′‐DDE was moderately cytotoxic at 100 μm. No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μm p,p′‐DDE, while ar showed strongest response at 100 μm. Metabolomics profiling showed that p,p′‐DDE at 100 μm 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. This work aimed to find biomarkers of the major DDT metabolite found in Atlantic salmon aquaculture feeds. Primary hepatocytes were exposed to four concentrations of p,p′‐DDE for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcriptomics and metabolomics profiling. p,p′‐DDE exposure was associated with endocrine disruption, impact on carbohydrate and lipid metabolism, and points to possible impact on DNA methylation mechanisms linked to methionine degradation in Atlantic salmon hepatocytes.
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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 μm) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μm). p,p′‐DDE was moderately cytotoxic at 100 μm. No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μm p,p′‐DDE, while ar showed strongest response at 100 μm. Metabolomics profiling showed that p,p′‐DDE at 100 μm 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. This work aimed to find biomarkers of the major DDT metabolite found in Atlantic salmon aquaculture feeds. 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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 μm) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μm). p,p′‐DDE was moderately cytotoxic at 100 μm. No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μm p,p′‐DDE, while ar showed strongest response at 100 μm. Metabolomics profiling showed that p,p′‐DDE at 100 μm 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. This work aimed to find biomarkers of the major DDT metabolite found in Atlantic salmon aquaculture feeds. 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Søfteland, Liv</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3496-8a2f53553664adf7995da90667627f641d9af94d245e19f3e0f2c939a51530693</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Aquaculture</topic><topic>Aquaculture feeds</topic><topic>Atlantic salmon</topic><topic>Bile</topic><topic>Bile acids</topic><topic>Biomarkers</topic><topic>Biosynthesis</topic><topic>Carbohydrate metabolism</topic><topic>Carbohydrates</topic><topic>Cytochrome</topic><topic>Cytochrome P450</topic><topic>Cytotoxicity</topic><topic>DDE</topic><topic>DDT</topic><topic>Degradation</topic><topic>Deoxyribonucleic acid</topic><topic>Diglycerides</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>Endocrine disruptors</topic><topic>Endocrine system</topic><topic>Environmental hazards</topic><topic>ESR1 protein</topic><topic>Exposure</topic><topic>Fish</topic><topic>gene expression, global DNA methylation</topic><topic>Hepatocytes</topic><topic>Isoleucine</topic><topic>Leucine</topic><topic>Lipid metabolism</topic><topic>Metabolism</topic><topic>Metabolites</topic><topic>Metabolomics</topic><topic>Methionine</topic><topic>Nitrous oxide</topic><topic>p,p′‐DDE</topic><topic>Pesticides</topic><topic>Phospholipids</topic><topic>Salmo salar</topic><topic>Salmon</topic><topic>Toxicity</topic><topic>Valine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Olsvik, Pål A.</creatorcontrib><creatorcontrib>Søfteland, Liv</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Environment Abstracts</collection><jtitle>Journal of applied toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Olsvik, Pål A.</au><au>Søfteland, Liv</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes</atitle><jtitle>Journal of applied toxicology</jtitle><addtitle>J Appl Toxicol</addtitle><date>2018-04</date><risdate>2018</risdate><volume>38</volume><issue>4</issue><spage>489</spage><epage>503</epage><pages>489-503</pages><issn>0260-437X</issn><eissn>1099-1263</eissn><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 μm) for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcription and metabolomics profiling (100 μm). p,p′‐DDE was moderately cytotoxic at 100 μm. No impact was seen on global DNA methylation. Vtg1 and esr1 transcription, markers of endocrine disruption, was most strongly induced at 10 μm p,p′‐DDE, while ar showed strongest response at 100 μm. Metabolomics profiling showed that p,p′‐DDE at 100 μm 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. This work aimed to find biomarkers of the major DDT metabolite found in Atlantic salmon aquaculture feeds. Primary hepatocytes were exposed to four concentrations of p,p′‐DDE for 48 hours, and endpoints included cytotoxicity, global DNA methylation, targeted transcriptomics and metabolomics profiling. p,p′‐DDE exposure was associated with endocrine disruption, impact on carbohydrate and lipid metabolism, and points to possible impact on DNA methylation mechanisms linked to methionine degradation in Atlantic salmon hepatocytes.</abstract><cop>England</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29148584</pmid><doi>10.1002/jat.3556</doi><tpages>15</tpages><orcidid>https://orcid.org/0000-0002-5641-9420</orcidid></addata></record>
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subjects Aquaculture
Aquaculture feeds
Atlantic salmon
Bile
Bile acids
Biomarkers
Biosynthesis
Carbohydrate metabolism
Carbohydrates
Cytochrome
Cytochrome P450
Cytotoxicity
DDE
DDT
Degradation
Deoxyribonucleic acid
Diglycerides
DNA
DNA methylation
Endocrine disruptors
Endocrine system
Environmental hazards
ESR1 protein
Exposure
Fish
gene expression, global DNA methylation
Hepatocytes
Isoleucine
Leucine
Lipid metabolism
Metabolism
Metabolites
Metabolomics
Methionine
Nitrous oxide
p,p′‐DDE
Pesticides
Phospholipids
Salmo salar
Salmon
Toxicity
Valine
title Metabolic effects of p,p′‐DDE on Atlantic salmon hepatocytes
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