PUBLICATION
Aryl hydrocarbon receptor activation and developmental toxicity in zebrafish in response to soil extracts containing unsubstituted and oxygenated PAHs
- Authors
- Wincent, E., Jonsson, M., Bottai, M., Lundstedt, S., Dreij, K.
- ID
- ZDB-PUB-150226-1
- Date
- 2015
- Source
- Environmental science & technology 49(6): 3869-77 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Coke/analysis
- Embryo, Nonmammalian/drug effects*
- Embryo, Nonmammalian/metabolism
- Gene Expression Regulation/drug effects*
- Industry
- Natural Gas/analysis
- Polycyclic Aromatic Hydrocarbons/toxicity*
- Receptors, Aryl Hydrocarbon/metabolism*
- Soil Pollutants/toxicity*
- Wood/analysis
- Zebrafish/embryology
- Zebrafish/metabolism*
- PubMed
- 25715055 Full text @ Env. Sci. Tech.
Citation
Wincent, E., Jonsson, M., Bottai, M., Lundstedt, S., Dreij, K. (2015) Aryl hydrocarbon receptor activation and developmental toxicity in zebrafish in response to soil extracts containing unsubstituted and oxygenated PAHs. Environmental science & technology. 49(6):3869-77.
Abstract
Many industrial sites are polluted by complex mixtures of polycyclic aromatic compounds (PACs). Besides polycyclic aromatic hydrocarbons (PAHs) these mixtures often contain significant amounts of more polar PACs including oxygenated PAHs (oxy-PAHs). The effects of oxy-PAHs are however poorly known. Here we used zebrafish embryos to examine toxicities and transcriptional changes induced by PAC containing soil extracts from three different industrial sites; a gasworks (GAS), a former wood preservation site (WOOD), and a coke oven (COKE) and to PAH and oxy-PAH containing fractions of these. All extracts induced aryl hydrocarbon receptor (Ahr)-regulated mRNAs, malformations, and mortality. The WOOD extract was most toxic and the GAS extract least toxic. The extracts induced glutathione transferases and heat shock protein 70, suggesting that the toxicity also involved oxidative stress. With all extracts Ahr2-knock-down reduced the toxicity, indicating a significant Ahr2-dependence on the effects. Ahr2-knock-down was most effective with the PAH fraction of the WOOD extract and with the oxy-PAH fraction of the COKE extract. Our results indicate that oxy-PAH containing mixtures can be as potent Ahr activators and developmental toxicants as PAHs. In addition to Ahr activating potency, the profile of cytochrome P4501 inhibitors may also determine the toxic potency of the extracts.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping