2019
DOI: 10.1016/j.scitotenv.2019.02.055
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1H NMR-based metabolomic analysis of nine organophosphate flame retardants metabolic disturbance in Hep G2 cell line

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Cited by 36 publications
(24 citation statements)
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“…In contrast, phosphate conjugation dominates phase II metabolism of tributyl phosphates (TBPs) in earthworms additionally (Wang et al, 2018a(Wang et al, , 2018b. The metabolism of OPFRs in earthworm corresponds with HepG cell in vitro metabolic experiment, in which two modules (glutathione biosynthesis and histidine degradation) and three metabolic pathways (alanine, aspartate, and glutamine metabolism; glycine, serine, and threonine metabolism; and glutamine and glutamate metabolism) were dominant (Jokanović, 2001;Gu et al, 2019). OPFRs transformed by soil animal may be detoxified to some extent, which prompts soil back to its initial condition (González-Alcaraz et al, 2020).…”
Section: Biotic Transformationsmentioning
confidence: 99%
“…In contrast, phosphate conjugation dominates phase II metabolism of tributyl phosphates (TBPs) in earthworms additionally (Wang et al, 2018a(Wang et al, , 2018b. The metabolism of OPFRs in earthworm corresponds with HepG cell in vitro metabolic experiment, in which two modules (glutathione biosynthesis and histidine degradation) and three metabolic pathways (alanine, aspartate, and glutamine metabolism; glycine, serine, and threonine metabolism; and glutamine and glutamate metabolism) were dominant (Jokanović, 2001;Gu et al, 2019). OPFRs transformed by soil animal may be detoxified to some extent, which prompts soil back to its initial condition (González-Alcaraz et al, 2020).…”
Section: Biotic Transformationsmentioning
confidence: 99%
“…However, some studies have also reported that the chronic neurotoxic mechanism of organophosphates cannot be related only to cholinesterase inhibition. Therefore, the molecular mechanism behind their toxicity is still elusive [158].…”
Section: Environmental Impacts Of Opfrsmentioning
confidence: 99%
“…to be transferred to offspring, resulting in developmental neurotoxicity (Du et al, 2015;Liu et al, 2013;Yu et al, 2017;Zhang et al, 2018a;Zhang et al, 2018b). Additional adverse effects of OPE exposure include developmental toxicity (Dasgupta et al, 2018;Dasgupta et al, 2017;Jacobsen et al, 2017;Li et al, 2018;Oliveri et al, 2018;Yan & Hales, 2018), oxidative stress (Chen et al, 2015a;Chen et al, 2015b;Gu et al, 2019;Yan et al, 2017), thyroid disruption (Fernie et al, 2017;Hill et al, 2018;Liu et al, 2019;Preston et al, 2017), neurotoxicity (Andresen et al, 2004;Hong et al, 2018;Shi et al, 2018;Slotkin et al, 2017), carcinogenicity (Hoffman et al, 2017b;Ni et al, 2007;Van den Eede et al, 2013b), endocrine disruption (Arukwe et al, 2016;Kojima et al, 2013;Kojima et al, 2016;, and cellular toxicity (Shen et al, 2019;Canbaz et al, 2017;Crump et al, 2012;Shen et al, 2019;Su et al, 2014a agonists, similar to their parent compound TBOEP as well as TEHP, and TNBP (Kojima et al, 2016). Metabolism can significantly influence the accumulation and adverse effects of chemicals in organisms, however the transformation of OPEs and distribution of their metabolites are still unknown.…”
Section: Metabolismmentioning
confidence: 99%