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Arch Toxicol. 2018 Feb;92(2):571-586. doi: 10.1007/s00204-017-2068-9. Epub 2017 Nov 1.

Comparative developmental toxicity of a comprehensive suite of polycyclic aromatic hydrocarbons.

Author information

1
Department of Environmental and Molecular Toxicology, Oregon State University, ALS 1007, Corvallis, OR, 97331, USA.
2
Department of Environmental and Molecular Toxicology, Oregon State University, ALS 1007, Corvallis, OR, 97331, USA. Robert.Tanguay@oregonstate.edu.

Abstract

Polycyclic aromatic hydrocarbons (PAHs) are widespread environmental contaminants that occur in complex mixtures. Several PAHs are known or suspected mutagens and/or carcinogens, but developmental toxicity data is lacking for PAHs, particularly their oxygenated and nitrated derivatives. Such data are necessary to understand and predict the toxicity of environmental mixtures. 123 PAHs were assessed for morphological and neurobehavioral effects for a range of concentrations between 0.1 and 50 µM, using a high throughput early-life stage zebrafish assay, including 33 parent, 22 nitrated, 17 oxygenated, 19 hydroxylated, 14 methylated, 16 heterocyclic, and 2 aminated PAHs. Additionally, each PAH was evaluated for AHR activation, by assessing CYP1A protein expression using whole animal immunohistochemistry (IHC). Responses to PAHs varied in a structurally dependent manner. High-molecular weight PAHs were significantly more developmentally toxic than the low-molecular weight PAHs, and CYP1A expression was detected in five distinct tissues, including vasculature, liver, skin, neuromasts and yolk.

KEYWORDS:

AHR; CYP1A; Developmental toxicity; PAH; Zebrafish

PMID:
29094189
PMCID:
PMC5820187
[Available on 2019-02-01]
DOI:
10.1007/s00204-017-2068-9

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