Use of alternative assays to identify and prioritize organophosphorus flame retardants for potential developmental and neurotoxicity

Abstract Due to their toxicity and persistence in the environment, brominated flame retardants (BFRs) are being phased out of commercial use, leading to the increased use of alternative chemicals such as the organophosphorus flame retardants (OPFRs). There is, however, limited information on the pot...

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Veröffentlicht in:Neurotoxicology and teratology 2015-11, Vol.52 (Pt B), p.181-193
Hauptverfasser: Behl, Mamta, Hsieh, Jui-Hua, Shafer, Timothy J, Mundy, William R, Rice, Julie R, Boyd, Windy A, Freedman, Jonathan H, Hunter, E. Sidney, Jarema, Kimberly A, Padilla, Stephanie, Tice, Raymond R
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container_end_page 193
container_issue Pt B
container_start_page 181
container_title Neurotoxicology and teratology
container_volume 52
creator Behl, Mamta
Hsieh, Jui-Hua
Shafer, Timothy J
Mundy, William R
Rice, Julie R
Boyd, Windy A
Freedman, Jonathan H
Hunter, E. Sidney
Jarema, Kimberly A
Padilla, Stephanie
Tice, Raymond R
description Abstract Due to their toxicity and persistence in the environment, brominated flame retardants (BFRs) are being phased out of commercial use, leading to the increased use of alternative chemicals such as the organophosphorus flame retardants (OPFRs). There is, however, limited information on the potential health effects of OPFRs. Due to the structural similarity of the OPFRs to organophosphorus insecticides, there is concern regarding developmental toxicity and neurotoxicity. In response, we evaluated a set of OPFRs (triphenyl phosphate [TPHP]), isopropylated phenyl phosphate [IPP], 2-ethylhexyl diphenyl phosphate [EHDP], tert-butylated phenyl diphenyl phosphate [BPDP], trimethyl phenyl phosphate [TMPP], isodecyl diphenyl phosphate [IDDP], (tris(1,3-dichloroisopropyl) phosphate [TDCIPP], and tris(2-chloroethyl)phosphate [TCEP]) in a battery of cell-based in vitro assays and alternative model organisms and compared the results to those obtained for two classical BFRs (3,3′,5,5′-tetrabromobisphenol A [TBBPA] and 2,2′4,4′-brominated diphenyl ether [BDE-47]). The assays used evaluated the effects of chemicals on the differentiation of mouse embryonic stem cells, the proliferation and growth of human neural stem cells, rat neuronal growth and network activity, and development of nematode ( Caenorhabditis elegans ) and zebrafish ( Danio rerio ). All assays were performed in a concentration-response format, allowing for the determination of the point of departure (POD: the lowest concentration where a chemically-induced response exceeds background noise). The majority of OPFRs (8/9) were active in multiple assays in the range of 1–10 μM, most of which had comparable activity to the BFRs TBBPA and BDE-47. TCEP was negative in all assays. The results indicate that the replacement OPFRs, with the exception of TCEP, showed comparable activity to the two BFRs in the assays tested. Based on these results, more comprehensive studies are warranted to further characterize the potential hazard of some of these OPFR compounds.
doi_str_mv 10.1016/j.ntt.2015.09.003
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In response, we evaluated a set of OPFRs (triphenyl phosphate [TPHP]), isopropylated phenyl phosphate [IPP], 2-ethylhexyl diphenyl phosphate [EHDP], tert-butylated phenyl diphenyl phosphate [BPDP], trimethyl phenyl phosphate [TMPP], isodecyl diphenyl phosphate [IDDP], (tris(1,3-dichloroisopropyl) phosphate [TDCIPP], and tris(2-chloroethyl)phosphate [TCEP]) in a battery of cell-based in vitro assays and alternative model organisms and compared the results to those obtained for two classical BFRs (3,3′,5,5′-tetrabromobisphenol A [TBBPA] and 2,2′4,4′-brominated diphenyl ether [BDE-47]). The assays used evaluated the effects of chemicals on the differentiation of mouse embryonic stem cells, the proliferation and growth of human neural stem cells, rat neuronal growth and network activity, and development of nematode ( Caenorhabditis elegans ) and zebrafish ( Danio rerio ). 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In response, we evaluated a set of OPFRs (triphenyl phosphate [TPHP]), isopropylated phenyl phosphate [IPP], 2-ethylhexyl diphenyl phosphate [EHDP], tert-butylated phenyl diphenyl phosphate [BPDP], trimethyl phenyl phosphate [TMPP], isodecyl diphenyl phosphate [IDDP], (tris(1,3-dichloroisopropyl) phosphate [TDCIPP], and tris(2-chloroethyl)phosphate [TCEP]) in a battery of cell-based in vitro assays and alternative model organisms and compared the results to those obtained for two classical BFRs (3,3′,5,5′-tetrabromobisphenol A [TBBPA] and 2,2′4,4′-brominated diphenyl ether [BDE-47]). The assays used evaluated the effects of chemicals on the differentiation of mouse embryonic stem cells, the proliferation and growth of human neural stem cells, rat neuronal growth and network activity, and development of nematode ( Caenorhabditis elegans ) and zebrafish ( Danio rerio ). All assays were performed in a concentration-response format, allowing for the determination of the point of departure (POD: the lowest concentration where a chemically-induced response exceeds background noise). The majority of OPFRs (8/9) were active in multiple assays in the range of 1–10 μM, most of which had comparable activity to the BFRs TBBPA and BDE-47. TCEP was negative in all assays. The results indicate that the replacement OPFRs, with the exception of TCEP, showed comparable activity to the two BFRs in the assays tested. 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The assays used evaluated the effects of chemicals on the differentiation of mouse embryonic stem cells, the proliferation and growth of human neural stem cells, rat neuronal growth and network activity, and development of nematode ( Caenorhabditis elegans ) and zebrafish ( Danio rerio ). All assays were performed in a concentration-response format, allowing for the determination of the point of departure (POD: the lowest concentration where a chemically-induced response exceeds background noise). The majority of OPFRs (8/9) were active in multiple assays in the range of 1–10 μM, most of which had comparable activity to the BFRs TBBPA and BDE-47. TCEP was negative in all assays. The results indicate that the replacement OPFRs, with the exception of TCEP, showed comparable activity to the two BFRs in the assays tested. 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ispartof Neurotoxicology and teratology, 2015-11, Vol.52 (Pt B), p.181-193
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subjects Action Potentials - drug effects
Animals
Caenorhabditis elegans
Cell Survival - drug effects
Cells, Cultured
Cerebral Cortex - drug effects
Cerebral Cortex - physiopathology
Danio rerio
developmental toxicity
Embryonic Development - drug effects
embryonic stem cells
Embryonic Stem Cells - drug effects
Emergency
Flame retardants
Flame Retardants - toxicity
Humans
Medical Education
Mice
Nematoda
Neurites - drug effects
Neurons - drug effects
Neurons - physiology
neurotoxicity
Organophosphorus Compounds - toxicity
Rats
Zebrafish
title Use of alternative assays to identify and prioritize organophosphorus flame retardants for potential developmental and neurotoxicity
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