PUBLICATION
Decabromodiphenyl ethane induced hyperactivity in developing zebrafish at environmentally relevant concentrations
- Authors
- Hua, J., Wang, X., Zhu, J., Wang, Q., Zhang, W., Lei, L., Zhu, B., Han, J., Yang, L., Zhou, B.
- ID
- ZDB-PUB-220903-8
- Date
- 2022
- Source
- Ecotoxicology and environmental safety 244: 114044 (Journal)
- Registered Authors
- Yang, LiHua, Zhou, BingSheng
- Keywords
- Decabromodiphenyl ethane, Developmental toxicity, Hyperactivity, Motor behavior, Zebrafish embryos/larvae
- MeSH Terms
-
- Animals
- Bromobenzenes
- Cholinergic Agents/metabolism
- Cholinergic Agents/pharmacology
- Flame Retardants*/metabolism
- Flame Retardants*/toxicity
- Larva
- Molecular Docking Simulation
- Neurotransmitter Agents/metabolism
- Tubulin/metabolism
- Tubulin/pharmacology
- Zebrafish*/metabolism
- PubMed
- 36055044 Full text @ Ecotoxicol. Environ. Saf.
Citation
Hua, J., Wang, X., Zhu, J., Wang, Q., Zhang, W., Lei, L., Zhu, B., Han, J., Yang, L., Zhou, B. (2022) Decabromodiphenyl ethane induced hyperactivity in developing zebrafish at environmentally relevant concentrations. Ecotoxicology and environmental safety. 244:114044.
Abstract
Decabromodiphenyl ethane (DBDPE), a widely used novel brominated flame retardant, is gaining concerns due to rapidly increased contents in various environmental and biota samples. In the present study, zebrafish (Danio rerio) embryos were exposed to 2.91, 9.71, 29.14 and 97.12 μg/L of DBDPE until 120 h post-fertilization (hpf) to investigate the potential developmental neurotoxicity and underlying mechanisms. Chemical analysis revealed concentration-dependently increased body burdens of DBDPE in zebrafish larvae, with bioaccumulation factors (BCFs) ranging from 414 to 726. Embryonic exposure to DBDPE caused hyperactivity without affecting the development of secondary motoneuron axons and muscle fibers. However, further results implicated that DBDPE may affect the locomotor regulatory network via different mechanisms at lower and higher concentrations. On the one hand, embryonic exposure to 2.91 μg/L DBDPE transiently promoted spontaneous coiling contractions, but showed no effects on touch-response and swimming activity in zebrafish larvae. The whole-body contents of neurotransmitters were significantly decreased. Significant decreased protein abundances of α1-TUBULIN and SYN2a and molecular docking results pointed out possible interactions of DBDPE with these two proteins. However, these changes may be unconcerned with the transient hyperactivity, and the exact molecular mechanisms need further investigation. On the other hand, 29.14 and 97.12 μg/L DBDPE exposure caused longer-lasting effects in promoting spontaneous coiling contractions, and also touch-response and swimming activity. At the same time, increased ACh contents (without changes of other neurotransmitters) and ChAT activity and inhibited transcription of nAChRs were observed at higher concentrations. Molecular docking indicated direct interaction of DBDPE with ChAT. The results suggested that DBDPE induced hyperactivity at higher concentrations was probably involved with disrupted cholinergic system, with ChAT as a potential target. Given that the body burden of DBDPE in lower concentration group was comparable with those detected in wild fish, the current results may provide useful information for ecological risk assessment.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping