PUBLICATION
Enzymatic activity and gene expression changes in zebrafish embryos and larvae exposed to pesticides diazinon and diuron
- Authors
- Velki, M., Meyer-Alert, H., Seiler, T.B., Hollert, H.
- ID
- ZDB-PUB-171103-2
- Date
- 2017
- Source
- Aquatic toxicology (Amsterdam, Netherlands) 193: 187-200 (Journal)
- Registered Authors
- Keywords
- Danio rerio, diazinon, diuron, enzymatic activity, gene expression
- MeSH Terms
-
- Acetylcholinesterase/metabolism
- Animals
- Carboxylesterase/metabolism
- Catalase/metabolism
- Cytochrome P-450 CYP1A1/metabolism
- Diazinon/toxicity
- Diuron/toxicity*
- Embryo, Nonmammalian/drug effects
- Embryo, Nonmammalian/metabolism
- Gene Expression
- Glutathione Peroxidase/metabolism
- Glutathione Reductase/metabolism
- Glutathione Transferase/metabolism
- Herbicides/toxicity*
- Insecticides/toxicity*
- Larva/drug effects
- Larva/metabolism
- Water Pollutants, Chemical/toxicity*
- Zebrafish/embryology
- Zebrafish/growth & development
- Zebrafish/metabolism*
- PubMed
- 29096092 Full text @ Aquat. Toxicol.
Citation
Velki, M., Meyer-Alert, H., Seiler, T.B., Hollert, H. (2017) Enzymatic activity and gene expression changes in zebrafish embryos and larvae exposed to pesticides diazinon and diuron. Aquatic toxicology (Amsterdam, Netherlands). 193:187-200.
Abstract
The zebrafish as a test organism enables the investigation of effects on a wide range of biological levels from molecular level to the whole-organism level. The use of fish embryos represents an attractive model for studies aimed at understanding toxic mechanisms and the environmental risk assessment of chemicals. In the present study, a zebrafish (Danio rerio) in vivo model was employed in order to assess the effects of two commonly used pesticides, the insecticide diazinon and the herbicide diuron, on zebrafish early life stages. Since it was previously established that diazinon and diuron cause effects at the whole-organism level, this study assessed the suborganismic responses to exposure to these pesticides and the enzymatic responses (biochemical level) and the gene expression changes (molecular level) were analyzed. Different exposure scenarios were employed and the following endpoints measured: acetylcholinesterase (AChE), carboxylesterase (CES), ethoxyresorufin-O-deethylase (EROD), glutathione-S-transferase (GST), catalase (CAT) and glutathione peroxidase (GPx) activities; and gene expressions of the corresponding genes: acetylcholinesterase (ache), carboxylesterase (ces2), cytochrome P450 (cyp1a), glutathione-S-transferase (gstp1), catalase (cat), glutathione peroxidase (gpx1a) and additionally glutathione reductase (gsr). Significant changes at both the biochemical and the molecular level were detected. In addition, different sensitivities of different developmental stages of zebrafish were determined and partial recovery of the enzyme activity 48h after the end of the exposure was observed. The observed disparity between gene expression changes and alterations in enzyme activities points to the necessity of monitoring changes at different levels of biological organization. Different exposure scenarios, together with a comparison of the responses at the biochemical and molecular level, provide valuable data on the effects of diazinon and diuron on low organizational levels in zebrafish embryos and larvae.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping