Literature DB >> 26386178

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

Mamta Behl1, Jui-Hua Hsieh2, Timothy J Shafer3, William R Mundy3, Julie R Rice4, Windy A Boyd4, Jonathan H Freedman5, E Sidney Hunter3, Kimberly A Jarema3, Stephanie Padilla3, Raymond R Tice4.   

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. Published by Elsevier Inc.

Entities:  

Keywords:  Caenorhabditis elegans; Flame retardants; developmental toxicity; embryonic stem cells; neurotoxicity; zebrafish

Mesh:

Substances:

Year:  2015        PMID: 26386178     DOI: 10.1016/j.ntt.2015.09.003

Source DB:  PubMed          Journal:  Neurotoxicol Teratol        ISSN: 0892-0362            Impact factor:   3.763


  51 in total

1.  Assessment of the DNA damaging potential of environmental chemicals using a quantitative high-throughput screening approach to measure p53 activation.

Authors:  Kristine L Witt; Jui-Hua Hsieh; Stephanie L Smith-Roe; Menghang Xia; Ruili Huang; Jinghua Zhao; Scott S Auerbach; Junguk Hur; Raymond R Tice
Journal:  Environ Mol Mutagen       Date:  2017-07-17       Impact factor: 3.216

2.  Polychlorinated biphenyl and polybrominated diphenyl ether profiles in serum from cattle, sheep, and goats across California.

Authors:  S Sethi; X Chen; P H Kass; B Puschner
Journal:  Chemosphere       Date:  2017-04-14       Impact factor: 7.086

3.  Organophosphate Ester Flame Retardants: Are They a Regrettable Substitution for Polybrominated Diphenyl Ethers?

Authors:  Arlene Blum; Mamta Behl; Linda Birnbaum; Miriam L Diamond; Allison Phillips; Veena Singla; Nisha S Sipes; Heather M Stapleton; Marta Venier
Journal:  Environ Sci Technol Lett       Date:  2019-10-21

4.  Transcriptome profiling of HepG2 cells exposed to the flame retardant 9,10-dihydro-9-oxa-10-phosphaphenanthrene 10-oxide (DOPO).

Authors:  Boris V Krivoshiev; Gerrit T S Beemster; Katrien Sprangers; Bart Cuypers; Kris Laukens; Ronny Blust; Steven J Husson
Journal:  Toxicol Res (Camb)       Date:  2018-03-12       Impact factor: 3.524

5.  Predictors of urinary flame retardant concentration among pregnant women.

Authors:  Kate Hoffman; Amelia Lorenzo; Craig M Butt; Linda Adair; Amy H Herring; Heather M Stapleton; Julie L Daniels
Journal:  Environ Int       Date:  2016-10-13       Impact factor: 9.621

6.  From the Cover: BDE-47 and BDE-49 Inhibit Axonal Growth in Primary Rat Hippocampal Neuron-Glia Co-Cultures via Ryanodine Receptor-Dependent Mechanisms.

Authors:  Hao Chen; Karin M Streifel; Vikrant Singh; Dongren Yang; Linley Mangini; Heike Wulff; Pamela J Lein
Journal:  Toxicol Sci       Date:  2017-04-01       Impact factor: 4.849

7.  Potential frameworks to support evaluation of mechanistic data for developmental neurotoxicity outcomes: A symposium report.

Authors:  Laura M Carlson; Frances A Champagne; Deborah A Cory-Slechta; Laura Dishaw; Elaine Faustman; William Mundy; Deborah Segal; Christina Sobin; Carol Starkey; Michele Taylor; Susan L Makris; Andrew Kraft
Journal:  Neurotoxicol Teratol       Date:  2020-02-14       Impact factor: 3.763

8.  Effects of Prenatal Exposure to a Mixture of Organophosphate Flame Retardants on Placental Gene Expression and Serotonergic Innervation in the Fetal Rat Brain.

Authors:  Kylie D Rock; Genevieve St Armour; Brian Horman; Allison Phillips; Matthew Ruis; Allison K Stewart; Dereje Jima; David C Muddiman; Heather M Stapleton; Heather B Patisaul
Journal:  Toxicol Sci       Date:  2020-07-01       Impact factor: 4.849

9.  Editor's Highlight: Comparative Toxicity of Organophosphate Flame Retardants and Polybrominated Diphenyl Ethers to Caenorhabditis elegans.

Authors:  Mamta Behl; Julie R Rice; Marjo V Smith; Caroll A Co; Matthew F Bridge; Jui-Hua Hsieh; Jonathan H Freedman; Windy A Boyd
Journal:  Toxicol Sci       Date:  2016-08-26       Impact factor: 4.849

10.  Brominated and organophosphate flame retardants target different neurodevelopmental stages, characterized with embryonic neural stem cells and neuronotypic PC12 cells.

Authors:  Theodore A Slotkin; Samantha Skavicus; Heather M Stapleton; Frederic J Seidler
Journal:  Toxicology       Date:  2017-08-26       Impact factor: 4.221

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