Literature DB >> 20549633

Brominated diphenyl ether (BDE) levels in liver, adipose, and milk from adult and juvenile rats exposed by gavage to the DE-71 technical mixture.

G S Bondy1, D Gaertner, W Cherry, E MacLellan, L Coady, D L Arnold, J Doucet, P R Rowsell.   

Abstract

Brominated diphenyl ethers (BDEs) are used as flame retardants in consumer products. Rodent studies indicate that the liver, thyroid, and nervous system of developing animals are targets of BDEs. To explore the relationship between exposure and health in developing animals, BDE accumulation in adult and juvenile rats was examined in conjunction with changes in liver weight and serum thyroxine (T4). Adult (F0) rats received the commercial BDE mixture DE-71 by gavage at doses of 0.5, 5, and 25 mg kg(-1) body weight (bw)/day for 21 weeks. F0 rats were mated and exposure continued throughout breeding, pregnancy, lactation, and postweaning until the pups (F1 generation) reached postnatal day (PND) 42. Milk was collected from lactating dams. Adipose and liver samples were collected from F0 and F1 males and females for BDE congener analysis. Congener prevalence in rat tissues mimicked congener prevalence in wildlife and humans. Tissue concentrations of all congeners except BDE-153 were lower than would be expected based on dose proportionality, confirming that BDE-153 has a high capacity for bioaccumulation. BDEs were transferred from maternal tissues to milk during lactation. Milk congener profiles differed from maternal tissue profiles indicating that degree of bromination and maternal sequestration influenced BDE transfer to milk. Female F1 rats accumulated more BDEs than F1 males, indicating that female rats were less able to metabolize and/or excrete BDEs. Significant effects on liver weight and serum T4 levels were observed in adults and juveniles in the middle and high dose groups, corresponding to BDE levels in the μg g(-1) range. Although it remains to be determined how human liver and thyroid are affected by exposure to much lower BDE levels, the present study confirmed that gender and reproductive status influence BDE accumulation in tissues and BDE transfer to the neonate via milk.
Copyright © 2010 Wiley Periodicals, Inc.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20549633     DOI: 10.1002/tox.20603

Source DB:  PubMed          Journal:  Environ Toxicol        ISSN: 1520-4081            Impact factor:   4.119


  4 in total

1.  Polybrominated diphenyl ether (DE-71) interferes with thyroid hormone action independent of effects on circulating levels of thyroid hormone in male rats.

Authors:  Ruby Bansal; Daniel Tighe; Amin Danai; Dorothea F K Rawn; Dean W Gaertner; Doug L Arnold; Mary E Gilbert; R Thomas Zoeller
Journal:  Endocrinology       Date:  2014-07-25       Impact factor: 4.736

2.  Perinatal exposure to low-dose DE-71 increases serum thyroid hormones and gonadal osteopontin gene expression.

Authors:  Charles A Blake; George L McCoy; Yvonne Y Hui; Holly A LaVoie
Journal:  Exp Biol Med (Maywood)       Date:  2011-03-02

Review 3.  Windows of sensitivity to toxic chemicals in the development of the endocrine system: an analysis of ATSDR's toxicological profile database.

Authors:  M C Buser; H R Pohl; H G Abadin
Journal:  Int J Environ Health Res       Date:  2020-06-04       Impact factor: 3.411

4.  In utero and childhood polybrominated diphenyl ether exposures and body mass at age 7 years: the CHAMACOS study.

Authors:  Ayca Erkin-Cakmak; Kim G Harley; Jonathan Chevrier; Asa Bradman; Katherine Kogut; Karen Huen; Brenda Eskenazi
Journal:  Environ Health Perspect       Date:  2015-02-27       Impact factor: 9.031

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.