PUBLICATION

Effect of combined exposure to lead and decabromodiphenyl ether on neurodevelopment of zebrafish larvae

Authors
Zhu, B., Wang, Q., Shi, X., Guo, Y., Xu, T., Zhou, B.
ID
ZDB-PUB-151101-1
Date
2016
Source
Chemosphere   144: 1646-1654 (Journal)
Registered Authors
Guo, YongYong, Zhou, BingSheng
Keywords
BDE-209, Co-exposure, Developmental neurotoxicity, Lead, ROS
MeSH Terms
  • Animals
  • Axons/drug effects*
  • Axons/metabolism
  • Central Nervous System/drug effects
  • Central Nervous System/growth & development
  • Central Nervous System/metabolism
  • Gene Expression Regulation, Developmental/drug effects*
  • Halogenated Diphenyl Ethers/toxicity*
  • Lead/toxicity*
  • Motor Activity/drug effects
  • Motor Neurons/drug effects
  • Motor Neurons/metabolism
  • Oxidative Stress
  • Random Allocation
  • Reactive Oxygen Species/metabolism
  • Water Pollutants, Chemical/toxicity*
  • Zebrafish/genetics
  • Zebrafish/growth & development
  • Zebrafish/metabolism*
PubMed
26519795 Full text @ Chemosphere
Abstract
The effect of combined exposure to decabromodiphenyl ether (BDE-209) and lead (Pb) on neurodevelopment of zebrafish (Danio rerio) larvae was investigated. Zebrafish embryos were exposed to Pb (0, 5, 10, 20 μg/L) and BDE-209 (0, 50, 100, 200 μg/L), either alone or in combination (Mix1: 5 + 50 μg/L, Mix2: 10 + 100 μg/L, Mix3: 20 + 200 μg/L) for up to 144 h post-fertilization. Growth of secondary motoneuron axons and expression of genes related to central nervous system development was significantly inhibited in Mix3 co-exposure group. A significant increase in reactive oxygen species (ROS), lipid peroxidation, DNA damage, and perturbation of the antioxidant system was detected in the Mix3 group compared to single-toxicant treatments or control. Depressed locomotor activity was recorded in the Mix2 and Mix3 groups. Addition of N-acetyl cysteine to Mix3 eliminated excessive ROS, and protected against lipid peroxidation, DNA damage, and locomotor dysfunction. Pb uptake was increased in the presence of BDE-209, but BDE-209 bioconcentration and the ability to metabolize BDE-209 were decreased in the presence of Pb. These results suggest that BDE-209 and Pb have a synergistic disruptive effect on neurodevelopment in zebrafish larvae by enhanced generation of ROS, which is a major factor that contributes to developmental neurotoxicity.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping