In vitro assessment of potential mechanism-specific effects of polybrominated diphenyl ethers

Environ Toxicol Chem. 2002 Nov;21(11):2431-3.

Abstract

This study examined the ability of environmentally relevant concentrations of 10 different polybrominated diphenyl ethers (PBDEs) to induce aryl hydrocarbon receptor (AhR)- and estrogen receptor (ER)-mediated gene expression in vitro. It also examined the ability of PBDEs to displace steroid hormones from serum proteins in vitro. At concentrations ranging up to 880 ng/ ml, none of the PBDEs significantly displaced tritiated 17beta-estradiol (E2) or testosterone from hormone-stripped carp serum. At concentrations ranging up to 500 ng/ml, 9 of 10 PBDEs tested failed to induce ER- or AhR-mediated gene expression in MVLN and H4IIE-luc cells, respectively. One congener, 3,3',4,4',5-pentabromodiphenylether (BDE 126), induced significant AhR-mediated gene expression at 500 ng/ml, but the magnitude of induction was only 13% of that caused by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Overall, the PBDEs tested were found to be at least 200,000 times less potent than TCDD and 50,000 times less potent than E2 for inducing AhR- and ER-mediated gene expression, respectively.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biological Assay
  • Blood Proteins / metabolism
  • Carps
  • Environmental Pollutants / toxicity*
  • Estradiol / metabolism*
  • Female
  • Flame Retardants / toxicity*
  • Gene Expression
  • Humans
  • Phenyl Ethers
  • Polybrominated Biphenyls / toxicity*
  • Rats
  • Receptors, Aryl Hydrocarbon / biosynthesis*
  • Receptors, Aryl Hydrocarbon / genetics
  • Receptors, Estrogen / biosynthesis*
  • Receptors, Estrogen / genetics
  • Structure-Activity Relationship
  • Testosterone / metabolism*
  • Tumor Cells, Cultured

Substances

  • Blood Proteins
  • Environmental Pollutants
  • Flame Retardants
  • Phenyl Ethers
  • Polybrominated Biphenyls
  • Receptors, Aryl Hydrocarbon
  • Receptors, Estrogen
  • Testosterone
  • Estradiol