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Hogberg, Helena T.; da Silveira E Sa, Rita de Cassia; Kleensang, Andre; Bouhifd, Mounir; Cemiloglu Ulker, Ozge; Smirnova, Lena; Behl, Mamta; Maertens, Alexandra; Zhao, Liang; Hartung, Thomas
{ "@context": "https://schema.org/", "@id": 3667, "@type": "ScholarlyArticle", "creator": [ { "@type": "Person", "affiliation": "Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing CAAT, Baltimore, MD 21205 USA", "name": "Hogberg, Helena T." }, { "@type": "Person", "name": "da Silveira E Sa, Rita de Cassia" }, { "@type": "Person", "affiliation": "Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing CAAT, Baltimore, MD 21205 USA", "name": "Kleensang, Andre" }, { "@type": "Person", "affiliation": "Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing CAAT, Baltimore, MD 21205 USA", "name": "Bouhifd, Mounir" }, { "@type": "Person", "name": "Cemiloglu Ulker, Ozge" }, { "@type": "Person", "affiliation": "Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing CAAT, Baltimore, MD 21205 USA", "name": "Smirnova, Lena" }, { "@type": "Person", "affiliation": "NIEHS, Natl Toxicol Program, Durham, NC USA", "name": "Behl, Mamta" }, { "@type": "Person", "affiliation": "Johns Hopkins Bloomberg Sch Publ Hlth, Ctr Alternat Anim Testing CAAT, Baltimore, MD 21205 USA", "name": "Maertens, Alexandra" }, { "@type": "Person", "name": "Zhao, Liang" }, { "@type": "Person", "name": "Hartung, Thomas" } ], "datePublished": "2021-01-01", "description": "Due to regulatory bans and voluntary substitutions, halogenated polybrominated diphenyl ether (PBDE) flame retardants (FR) are increasingly substituted by mainly organophosphorus FR (OPFR). Leveraging a 3D rat primary neural organotypic in vitro model (rat brainsphere), we compare developmental neurotoxic effects of BDE-47-the most abundant PBDE congener-with four OPFR (isopropylated phenyl phosphate-IPP, triphenyl phosphate-TPHP, isodecyl diphenyl phosphate-IDDP, and tricresyl phosphate (also known as trimethyl phenyl phosphate)-TMPP). Employing mass spectroscopy-based metabolomics and transcriptomics, we observe at similar human-relevant non-cytotoxic concentrations (0.1-5 mu M) stronger developmental neurotoxic effects by OPFR. This includes toxicity to neurons in the low mu M range; all FR decrease the neurotransmitters glutamate and GABA (except BDE-47 and TPHP). Furthermore,n-acetyl aspartate (NAA), considered a neurologic diagnostic molecule, was decreased by all OPFR. At similar concentrations, the FR currently in use decreased plasma membrane dopamine active transporter expression, while BDE-47 did not. Several findings suggest astrogliosis induced by the OPFR, but not BDE-47. At the 5 mu M concentrations, the OPFR more than BDE-47 interfered with myelination. An increase of cytokine gene and receptor expressions suggests that exposure to OPFR may induce an inflammatory response. Pathway/category overrepresentation shows disruption in 1) transmission of action potentials, cell-cell signaling, synaptic transmission, receptor signaling, (2) immune response, inflammation, defense response, (3) cell cycle and (4) lipids metabolism and transportation. Taken together, this appears to be a case of regretful substitution with substances not less developmentally neurotoxic in a primary rat 3D model.", "headline": "Organophosphorus flame retardants are developmental neurotoxicants in a rat primary brainsphere in vitro model", "identifier": 3667, "image": "https://aperta.ulakbim.gov.tr/static/img/logo/aperta_logo_with_icon.svg", "license": "http://www.opendefinition.org/licenses/cc-by", "name": "Organophosphorus flame retardants are developmental neurotoxicants in a rat primary brainsphere in vitro model", "url": "https://aperta.ulakbim.gov.tr/record/3667" }
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