PUBLICATION

Effects of multi-walled carbon nanotubes on the enantioselective toxicity of the chiral insecticide indoxacarb toward zebrafish (Danio rerio)

Authors
Wang, J., Jia, B., Li, Y., Ren, B., Liang, H., Yan, D., Xie, H., Zhang, X., Liang, H.
ID
ZDB-PUB-200511-11
Date
2020
Source
Journal of hazardous materials   397: 122724 (Journal)
Registered Authors
Keywords
Altered enantioselective toxicity, Indoxacarb, MWCNTs, Zebrafish
MeSH Terms
  • Animals
  • Insecticides*
  • Nanotubes, Carbon*/toxicity
  • Oxazines
  • Stereoisomerism
  • Zebrafish
PubMed
32387829 Full text @ J. Hazard. Mater.
Abstract
The mass production and usage of carbon nanotubes (CNTs) have led to the inevitable release into the environment, and the effects of CNTs on the toxicity of co-existing pollutants have been well documented. However, knowledge of the effects of CNTs on the enantioselective toxicity of chiral compounds is limited. Using zebrafish as an experimental model, the enantioselective expression of the apoptosis, CYP3C and EAAT-related genes were analyzed following exposure to multi-walled carbon nanotubes (MWCNTs) (0.05 and 0.5 mg/L), rac-/R-/S-indoxacarb (0.01 mg/L), or the combination of rac-/R-/S-indoxacarb mixed with MWCNTs for 28d. Sex-specific differences were observed in both the liver and brain of zebrafish. The expression of apoptosis and CYP3C-related genes was 16.55-44.29 times higher in the livers of males treated with R-indoxacarb than in S-indoxacarb treated groups. The EAAT-related genes were expressed at 1.38-2.56 times higher levels in the brain of females treated with R-indoxacarb than in S-indoxacarb-treated groups. In the presence of MWCNTs, the expression of caspase-3, cyp3c3, cyp3c4, eaat1a, eaat1b and eaat2 in the livers of males and brains of females treated with S-indoxacarb were 1.65-15.33 times higher than in fish treated with R-indoxacarb. Based on these results, MWCNTs affected the enantioselective toxicity of indoxacarb toward zebrafish.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping