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Co-Exposure of Phenanthrene and the cyp-Inducer 3-Methylchrysene Leads to Altered Biotransformation and Increased Toxicity in Fish Egg and Larvae.
Donald, Carey E; Sørhus, Elin; Perrichon, Prescilla; Nakken, Charlotte L; Goksøyr, Anders; Jørgensen, Kåre B; Mayer, Philipp; da Silva, Denis A M; Meier, Sonnich.
Afiliación
  • Donald CE; Marine Toxicology, Institute of Marine Research, 5004 Bergen, Norway.
  • Sørhus E; Marine Toxicology, Institute of Marine Research, 5004 Bergen, Norway.
  • Perrichon P; Reproduction and Developmental Biology, Institute of Marine Research, Austevoll Research Station, 5392 Storebø, Norway.
  • Nakken CL; Department of Chemistry, University of Bergen, 5007 Bergen, Norway.
  • Goksøyr A; Department of Biological Sciences, University of Bergen, 5006 Bergen, Norway.
  • Jørgensen KB; Department of Chemistry, Bioscience and Environmental Engineering, Faculty of Science and Technology, University of Stavanger, 4021 Stavanger, Norway.
  • Mayer P; Department of Environmental & Resource Engineering, Technical University of Denmark, 2800 Kgs. Lyngby, Denmark.
  • da Silva DAM; Environmental Chemistry Program, Northwest Fisheries Science Center (NOAA), Seattle, Washington 98112, United States.
  • Meier S; Marine Toxicology, Institute of Marine Research, 5004 Bergen, Norway.
Environ Sci Technol ; 57(30): 11022-11031, 2023 Aug 01.
Article en En | MEDLINE | ID: mdl-37465931
Polycyclic aromatic hydrocarbons (PAHs) have frequently been suspected of governing crude oil toxicity because of similar morphological defects in fish. However, PAH concentrations are often not high enough to explain the observed crude oil toxicity. We hypothesize that one PAH can enhance the metabolism and toxicity of another PAH when administered as a mixture. Early life stage Atlantic haddock (Melanogrammus aeglefinus) were in this study exposed to phenanthrene in the presence and absence of 3-methylchrysene that is known to induce the metabolic enzyme cytochrome P450 1A via cyp1a gene expression. Uptake, metabolism, and multiple toxicity endpoints were then measured in a time-course study up to 3 days post-hatching. Passive dosing provided aqueous concentrations ≈180 µg/L for phenanthrene and ≈0.6 µg/L for 3-methylchrysene, which resulted in tissue concentrations ≈60 µg/g ww for phenanthrene and ≈0.15 µg/g ww for 3-methylchrysene. The low concentration of 3-methylchrysene led to the elevated expression of cyp1a but no toxicity. Levels of phenanthrene metabolites were 5-fold higher, and morphological defects and cardiotoxicity were consistently greater when co-exposed to both compounds relative to phenanthrene alone. This work highlights the metabolic activation of PAH toxicity by a co-occurring PAH, which can lead to excess toxicity, synergistic effects, and the overproportional contribution of PAHs to crude oil toxicity.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Environ Sci Technol Año: 2023 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Environ Sci Technol Año: 2023 Tipo del documento: Article País de afiliación: Noruega Pais de publicación: Estados Unidos