Literature DB >> 9831538

Toxic equivalency factors (TEFs) for PCBs, PCDDs, PCDFs for humans and wildlife.

M Van den Berg1, L Birnbaum, A T Bosveld, B Brunström, P Cook, M Feeley, J P Giesy, A Hanberg, R Hasegawa, S W Kennedy, T Kubiak, J C Larsen, F X van Leeuwen, A K Liem, C Nolt, R E Peterson, L Poellinger, S Safe, D Schrenk, D Tillitt, M Tysklind, M Younes, F Waern, T Zacharewski.   

Abstract

An expert meeting was organized by the World Health Organization (WHO) and held in Stockholm on 15-18 June 1997. The objective of this meeting was to derive consensus toxic equivalency factors (TEFs) for polychlorinated dibenzo-p-dioxins (PCDDs) and dibenzofurans (PCDFs) and dioxinlike polychlorinated biphenyls (PCBs) for both human, fish, and wildlife risk assessment. Based on existing literature data, TEFs were (re)evaluated and either revised (mammals) or established (fish and birds). A few mammalian WHO-TEFs were revised, including 1,2,3,7,8-pentachlorinated DD, octachlorinated DD, octachlorinated DF, and PCB 77. These mammalian TEFs are also considered applicable for humans and wild mammalian species. Furthermore, it was concluded that there was insufficient in vivo evidence to continue the use of TEFs for some di-ortho PCBs, as suggested earlier by Ahlborg et al. [Chemosphere 28:1049-1067 (1994)]. In addition, TEFs for fish and birds were determined. The WHO working group attempted to harmonize TEFs across different taxa to the extent possible. However, total synchronization of TEFs was not feasible, as there were orders of a magnitude difference in TEFs between taxa for some compounds. In this respect, the absent or very low response of fish to mono-ortho PCBs is most noticeable compared to mammals and birds. Uncertainties that could compromise the TEF concept were also reviewed, including nonadditive interactions, differences in shape of the dose-response curve, and species responsiveness. In spite of these uncertainties, it was concluded that the TEF concept is still the most plausible and feasible approach for risk assessment of halogenated aromatic hydrocarbons with dioxinlike properties.

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Year:  1998        PMID: 9831538      PMCID: PMC1533232          DOI: 10.1289/ehp.98106775

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  130 in total

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Authors:  D W Brewster; L S Birnbaum
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4.  Potency of a complex mixture of polychlorinated dibenzo-p-dioxin, dibenzofuran, and biphenyl congeners compared to 2,3,7,8-tetrachlorodibenzo-p-dioxin in causing fish early life stage mortality.

Authors:  M K Walker; P M Cook; B C Butterworth; E W Zabel; R E Peterson
Journal:  Fundam Appl Toxicol       Date:  1996-04

5.  H4IIE rat hepatoma cell bioassay-derived 2,3,7,8-tetrachlorodibenzo-p-dioxin equivalents in colonial fish-eating waterbird eggs from the Great Lakes.

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Journal:  Arch Environ Contam Toxicol       Date:  1991-07       Impact factor: 2.804

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Journal:  Carcinogenesis       Date:  1991-05       Impact factor: 4.944

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Authors:  B U Stahl; A Kettrup; K Rozman
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10.  Structure-dependent induction of CYP2B by polychlorinated biphenyl congeners in female Sprague-Dawley rats.

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Journal:  Biochem Pharmacol       Date:  1995-11-27       Impact factor: 5.858

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Review 2.  Ah receptor ligands and their impacts on gut resilience: structure-activity effects.

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4.  Eicosapentaenoic acid protects against 2,3,7,8-tetrachlorodibenzo-p-dioxin-induced hepatic toxicity in cultured rat hepatocytes.

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6.  Sensitivity to dioxin decreases as zebrafish mature.

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7.  2,3,7,8-Tetrachlorodibenzo-p-dioxin-induced MUC5AC expression: aryl hydrocarbon receptor-independent/EGFR/ERK/p38-dependent SP1-based transcription.

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Review 8.  Hormones and endocrine-disrupting chemicals: low-dose effects and nonmonotonic dose responses.

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9.  Analysis of dioxins in contaminated soils with the calux and caflux bioassays, an immunoassay, and gas chromatography/high-resolution mass spectrometry.

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10.  Human health risk assessment of soil dioxin/furans contamination and dioxin-like activity determined by ethoxyresorufin-O-deethylase bioassay.

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