(Tables 1,2) Polar bear (Ursus maritimus), beluga whale (Delphinapterus leucas) and ringed seal (Pusa hispida) liver microsomal protein content and EROD activity

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Auteurs principaux: McKinney, Melissa A, Dietz, Rune, Sonne, Christian, De Guise, Sylvain, Skirnisson, Karl, Karlsson, Karl, Steingrimsson, Egill, Letcher, Robert J
Format: Dataset Open Access
Langue:en
Publié: PANGAEA 2011
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author McKinney, Melissa A
Dietz, Rune
Sonne, Christian
De Guise, Sylvain
Skirnisson, Karl
Karlsson, Karl
Steingrimsson, Egill
Letcher, Robert J
author_facet McKinney, Melissa A
Dietz, Rune
Sonne, Christian
De Guise, Sylvain
Skirnisson, Karl
Karlsson, Karl
Steingrimsson, Egill
Letcher, Robert J
collection Datos científicos de ciencias marinas y ambientales
contents The present study assessed and compared the oxidative and reductive biotransformation of brominated flame retardants, including established polybrominated diphenyl ethers (PBDEs) and emerging decabromodiphenyl ethane (DBDPE) using an in vitro system based on liver microsomes from various arctic marine-feeding mammals: polar bear (Ursus maritimus), beluga whale (Delphinapterus leucas), and ringed seal (Pusa hispida), and in laboratory rat as a mammalian model species. Greater depletion of fully brominated BDE209 (14-25% of 30pmol) and DBDPE (44-74% of 90pmol) occurred in individuals from all species relative to depletion of lower brominated PBDEs (BDEs 99,100, and 154; 0-3% of 30pmol). No evidence of simply debrominated metabolites was observed. Investigation of phenolic metabolites in rat and polar bear revealed formation of two phenolic, likely multiply debrominated, DBDPE metabolites in polar bear and one phenolic BDE154 metabolite in polar bear and rat microsomes. For BDE209 and DBDPE, observed metabolite concentrations were low to nondetectable, despite substantial parent depletion. These findings suggested possible underestimation of the ecosystem burden of total-BDE209, as well as its transformation products, and a need for research to identify and characterize the persistence and toxicity of major BDE209 metabolites. Similar cause for concern may exist regarding DBDPE, given similarities of physicochemical and environmental behavior to BDE209, current evidence of biotransformation, and increasing use of DBDPE as a replacement for BDE209.
format Dataset Open Access
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institution PANGAEA
language en
publishDate 2011
publisher PANGAEA
record_format pangaea
spellingShingle (Tables 1,2) Polar bear (Ursus maritimus), beluga whale (Delphinapterus leucas) and ringed seal (Pusa hispida) liver microsomal protein content and EROD activity
McKinney, Melissa A
Dietz, Rune
Sonne, Christian
De Guise, Sylvain
Skirnisson, Karl
Karlsson, Karl
Steingrimsson, Egill
Letcher, Robert J
7-ethoxyresorufin-O-deethylase, activity per protein mass; Age, comment; Area/locality; Biological sample; BIOS; Cumberland_Sound; DATE/TIME; Event label; Fluorescence microplate assay; Hudson Bay; Iceland; International Polar Year (2007-2008); IPY; Labrador Sea; MULT; Multiple investigations; Proteins, total; Proteins, total, standard deviation; Sample ID; Sample type; Sex; Species; Species, common name; Standard deviation; W_Hudson_Bay
The present study assessed and compared the oxidative and reductive biotransformation of brominated flame retardants, including established polybrominated diphenyl ethers (PBDEs) and emerging decabromodiphenyl ethane (DBDPE) using an in vitro system based on liver microsomes from various arctic marine-feeding mammals: polar bear (Ursus maritimus), beluga whale (Delphinapterus leucas), and ringed seal (Pusa hispida), and in laboratory rat as a mammalian model species. Greater depletion of fully brominated BDE209 (14-25% of 30pmol) and DBDPE (44-74% of 90pmol) occurred in individuals from all species relative to depletion of lower brominated PBDEs (BDEs 99,100, and 154; 0-3% of 30pmol). No evidence of simply debrominated metabolites was observed. Investigation of phenolic metabolites in rat and polar bear revealed formation of two phenolic, likely multiply debrominated, DBDPE metabolites in polar bear and one phenolic BDE154 metabolite in polar bear and rat microsomes. For BDE209 and DBDPE, observed metabolite concentrations were low to nondetectable, despite substantial parent depletion. These findings suggested possible underestimation of the ecosystem burden of total-BDE209, as well as its transformation products, and a need for research to identify and characterize the persistence and toxicity of major BDE209 metabolites. Similar cause for concern may exist regarding DBDPE, given similarities of physicochemical and environmental behavior to BDE209, current evidence of biotransformation, and increasing use of DBDPE as a replacement for BDE209.
title (Tables 1,2) Polar bear (Ursus maritimus), beluga whale (Delphinapterus leucas) and ringed seal (Pusa hispida) liver microsomal protein content and EROD activity
topic 7-ethoxyresorufin-O-deethylase, activity per protein mass; Age, comment; Area/locality; Biological sample; BIOS; Cumberland_Sound; DATE/TIME; Event label; Fluorescence microplate assay; Hudson Bay; Iceland; International Polar Year (2007-2008); IPY; Labrador Sea; MULT; Multiple investigations; Proteins, total; Proteins, total, standard deviation; Sample ID; Sample type; Sex; Species; Species, common name; Standard deviation; W_Hudson_Bay
url https://doi.org/10.1594/PANGAEA.816176