Document Detail


Decabromodiphenyl ether in the rat: absorption, distribution, metabolism, and excretion.
MedLine Citation:
PMID:  12814967     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Among the group of polybrominated diphenyl ethers used as flame-retardants, the fully brominated diphenyl ether, decabromodiphenyl ether (decaBDE), is the most commonly used. Despite the large usage of decaBDE, neither the metabolic pathways nor the absorption have been addressed, and there are very few studies on its toxicology. In this work, it is shown that after a single oral dose of 14C-labeled decaBDE to rats, at least 10% of the decaBDE dose is absorbed. The major excretion route in conventional rats is via feces that contained 90% of the decaBDE dose. The excretion in bile was close to 10% of the dose and represented mainly metabolites. It cannot be excluded that greater than 10% of the oral dose had been absorbed since 65% of the radioactivity excreted in feces was metabolites. The highest concentrations on a lipid weight basis were found in plasma and blood-rich tissues, and the adipose tissue had the lowest concentration of decaBDE. After derivatization of a phenolic fraction, gas chromatography-mass spectrometry (GC/MS) analyses indicated that metabolites with five to seven bromine atoms had formed, and they possessed a guaiacol structure (a hydroxy and a methoxy group) in one of the rings. In addition, traces of nonabrominated diphenyl ethers and monohydroxylated metabolites were found by GC/MS. Metabolites, characterized by their chemical properties, were interpreted to be covalently bound to macromolecules, either proteins or lipids. In addition, water solubility was suggested. The metabolic pathway was indicated to include a reactive intermediate.
Authors:
Anna Morck; Heldur Hakk; Ulrika Orn; Eva Klasson Wehler
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't    
Journal Detail:
Title:  Drug metabolism and disposition: the biological fate of chemicals     Volume:  31     ISSN:  0090-9556     ISO Abbreviation:  Drug Metab. Dispos.     Publication Date:  2003 Jul 
Date Detail:
Created Date:  2003-06-19     Completed Date:  2004-03-10     Revised Date:  2008-11-21    
Medline Journal Info:
Nlm Unique ID:  9421550     Medline TA:  Drug Metab Dispos     Country:  United States    
Other Details:
Languages:  eng     Pagination:  900-7     Citation Subset:  IM    
Affiliation:
Department of Environmental Chemistry, Stockholm University, Sweden.
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MeSH Terms
Descriptor/Qualifier:
Absorption
Acetylation
Animals
Bile / chemistry
Bromobenzenes / metabolism*
Carbon Isotopes
Emulsions
Feces / chemistry*
Halogenated Diphenyl Ethers
Hydrocarbons, Brominated
Intestine, Small / chemistry,  drug effects
Kidney / chemistry,  drug effects
Liver / chemistry,  drug effects
Lung / chemistry,  drug effects
Male
Methylation
Molecular Structure
Phenols / analysis,  metabolism
Phenyl Ethers
Polybrominated Biphenyls
Protein Binding
Rats
Rats, Sprague-Dawley
Solubility
Tissue Distribution*
Chemical
Reg. No./Substance:
0/Bromobenzenes; 0/Carbon Isotopes; 0/Emulsions; 0/Halogenated Diphenyl Ethers; 0/Hydrocarbons, Brominated; 0/Phenols; 0/Phenyl Ethers; 0/Polybrominated Biphenyls; 1163-19-5/decabromobiphenyl ether

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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