Journal article
3,3′,4,4′,5-Pentachlorobiphenyl (PCB 126) Decreases Hepatic and Systemic Ratios of Epoxide to Diol Metabolites of Unsaturated Fatty Acids in Male Rats
Toxicological sciences, Vol.152(2), pp.309-322
08/2016
DOI: 10.1093/toxsci/kfw084
PMCID: PMC4960907
PMID: 27208083
Abstract
Disruption of the homeostasis of oxygenated regulatory lipid mediators (oxylipins), potential markers of exposure to aryl hydrocarbon receptor (AhR) agonists, such as 3,3′,4,4′,5-pentachlorobiphenyl (PCB 126), is associated with a range of diseases, including nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Here we test the hypothesis that PCB 126 exposure alters the levels of oxylipins in rats. Male Sprague-Dawley rats (5-weeks old) were treated over a 3-month period every 2 weeks with intraperitoneal injections of PCB 126 in corn oil (cumulative doses of 0, 19.8, 97.8, and 390 µg/kg b.w.; 6 injections total). PCB 126 treatment caused a reduction in growth rates at the highest dose investigated, a dose-dependent decrease in thymus weights, and a dose-dependent increase in liver weights. Liver PCB 126 levels increased in a dose-dependent manner, while levels in plasma were below or close to the detection limit. The ratios of several epoxides to diol metabolites formed
via
the cytochrome P450 (P450) monooxygenase/soluble epoxide hydrolase (sEH) pathway from polyunsaturated fatty acids displayed a dose-dependent decrease in the liver and plasma, whereas levels of oxylipins formed by other metabolic pathways were generally not altered by PCB 126 treatment. The effects of PCB 126 on epoxide-to-diol ratios were associated with an increased CYP1A activity in liver microsomes and an increased sEH activity in liver cytosol and peroxisomes. These results suggest that oxylipins are potential biomarkers of exposure to PCB 126 and that the P450/sEH pathway is a therapeutic target for PCB 126-mediated hepatotoxicity that warrants further attention.
Details
- Title: Subtitle
- 3,3′,4,4′,5-Pentachlorobiphenyl (PCB 126) Decreases Hepatic and Systemic Ratios of Epoxide to Diol Metabolites of Unsaturated Fatty Acids in Male Rats
- Creators
- Xianai Wu - Department of Occupational and Environmental Health, College of Public Health, The University of Iowa, Iowa City, IowaJun Yang - Department of Entomology and Nematology, UC Davis Comprehensive Cancer Center, University of California, Davis, CaliforniaChristophe Morisseau - Department of Entomology and Nematology, UC Davis Comprehensive Cancer Center, University of California, Davis, CaliforniaLarry W Robertson - Department of Occupational and Environmental Health, College of Public Health, The University of Iowa, Iowa City, IowaBruce Hammock - Department of Entomology and Nematology, UC Davis Comprehensive Cancer Center, University of California, Davis, CaliforniaHans-Joachim Lehmler - Department of Occupational and Environmental Health, College of Public Health, The University of Iowa, Iowa City, Iowa
- Resource Type
- Journal article
- Publication Details
- Toxicological sciences, Vol.152(2), pp.309-322
- DOI
- 10.1093/toxsci/kfw084
- PMID
- 27208083
- PMCID
- PMC4960907
- NLM abbreviation
- Toxicol Sci
- ISSN
- 1096-6080
- eISSN
- 1096-0929
- Publisher
- Oxford University Press
- Language
- English
- Date published
- 08/2016
- Academic Unit
- Occupational and Environmental Health; Iowa Neuroscience Institute; Iowa Superfund Research Program
- Record Identifier
- 9984000921002771
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