2015
DOI: 10.1016/j.envint.2014.09.002
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Identification of a group of brominated flame retardants as novel androgen receptor antagonists and potential neuronal and endocrine disrupters

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Cited by 36 publications
(23 citation statements)
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“…Degradation of BRF emits vapors that have negative health impacts. Studies have shown that BFR has endocrine disrupting effects (44), neurotoxic effects (45), and causes tissue accumulation (46). However, limited toxicity information is present, and results are mostly incomplete and often conflicting.…”
Section: Indoor Air Pollutants -Sources and Health Effectsmentioning
confidence: 99%
“…Degradation of BRF emits vapors that have negative health impacts. Studies have shown that BFR has endocrine disrupting effects (44), neurotoxic effects (45), and causes tissue accumulation (46). However, limited toxicity information is present, and results are mostly incomplete and often conflicting.…”
Section: Indoor Air Pollutants -Sources and Health Effectsmentioning
confidence: 99%
“…The BFR exposures that trigger neural effects and behavioral changes in animals are comparable to the higher end of the range of concentrations found in some infants and toddlers (Costa and Giordano, 2007; Costa et al, 2009). Some neurotoxicity of BFRs comes from disrupting the L‐type amino acid transporter system, which has been implicated in several neural disorders (Kharlyngdoh et al, 2015). Oxidative stress and Ca ++ regulation have also been implicated (Dingemans et al, 2011; it is interesting to note that disruption of neural Ca ++ homeostasis is a known neurotoxic factor in traumatic brain injury).…”
Section: Basis Of Links Between Volatiles and Neurotoxic Risk Factorsmentioning
confidence: 99%
“…In particular, Nguon et al focus on cerebellar defects, altered startle responses and impaired fine motor coordination, which have each been reported in autism. Endocrine effects are also reported for brominated flame retardants and phthalates; both phthalates and BFRs modulate androgen receptors (Chen et al, 2014; Costa and Giordano, 2007; Costa et al, 2009; Kharlyngdoh et al, 2015; Patisaul et al, 2015; Pradhan et al, 2013, 2015) and may modulate developmental effects in a sex‐specific manner (Chevrier et al, 2016; Lilienthal et al, 2006; Nguon et al, 2005; Patisaul et al, 2015; Swan et al, 2010). Lilienthal et al (2006) found PBDE exposures during pregnancy affected male rats much more than female rates, with sex differential effects in levels of circulating sex hormones, changes in physical development and behavior.…”
Section: Basis Of Links Between Volatiles and Neurotoxic Risk Factorsmentioning
confidence: 99%
“…EDs can disrupt the endocrine system through different mechanisms [ 7 , 8 , 9 , 10 , 11 , 12 ]. One of the well-known mechanisms is mediated by the hormone receptors such estrogen receptor (ER) and androgen receptor (AR), in which EDs exhibit their estrogenic and androgenic effects through binding to the ER and AR in the target cells [ 13 , 14 , 15 , 16 ]. Therefore, a huge amount of estrogenic and androgenic activity data of structurally diverse chemicals have been generated and organized in sophisticated databases such as the FDA’s Endocrine Disruptors Knowledge Base (EDKB) [ 17 ] and Estrogenic Activity Database (EADB) [ 18 ].…”
Section: Introductionmentioning
confidence: 99%