PUBLICATION
Stronger estrogenic and antiandrogenic effects on zebrafish larvae displayed by 6:2 polyfluoroalkyl phosphate diester than the 8:2 congener at environmentally relevant concentrations
- Authors
- Chen, P., Wang, R., Yang, J., Zhong, W., Liu, M., Yi, S., Zhu, L.
- ID
- ZDB-PUB-190820-13
- Date
- 2019
- Source
- The Science of the total environment 695: 133907 (Journal)
- Registered Authors
- Keywords
- Androgen receptor, Estrogen receptor, Molecular docking, Molecular dynamic simulations, Polyfluoroalkyl phosphate esters, Zebrafish
- MeSH Terms
-
- Animals
- Toxicity Tests
- Zebrafish/physiology
- Organophosphates/toxicity*
- Water Pollutants, Chemical/toxicity*
- Estrogens/toxicity*
- PubMed
- 31425999 Full text @ Sci. Total Environ.
Citation
Chen, P., Wang, R., Yang, J., Zhong, W., Liu, M., Yi, S., Zhu, L. (2019) Stronger estrogenic and antiandrogenic effects on zebrafish larvae displayed by 6:2 polyfluoroalkyl phosphate diester than the 8:2 congener at environmentally relevant concentrations. The Science of the total environment. 695:133907.
Abstract
Polyfluoroalkyl phosphate esters (PAPs) are one kind of emerging polyfluoroalkyl substances in the environment. However, their in vivo toxicities are largely unknown, especially at environmental relevant concentrations. To fill this gap, zebrafish embryos were exposed to 6:2 or 8:2 diPAP at environmentally relevant concentrations (0.5, 5, 50 ng/L) for 7 d. 6:2 and 8:2 diPAPs upregulated the mRNA and protein levels of aromatase in the exposed larvae, and elevated estradiol (E2) and vitellogenin (VTG) levels, but reduced testosterone (T) and 11-ketotestosterone (11-KT) levels, demonstrating estrogenic and antiandrogenic effects. Among the three ER subtypes, ERβ2 displayed the highest in vivo mRNA expression and the lowest in silico binding energies, suggesting that it was the main target ER subtype responsible for the estrogenic effect. Molecular simulation results indicated that diPAPs and E2 could bind to one common residue, arginine (Arg) 87, in the binding pocket of ERβ2, inducing similar estrogenic disruption mechanisms as E2. Both compounds could form hydrophobic interaction with glutamic acid (Glu) 12 and tryptophan (Trp) 80 and two hydrogen bonds with Arg81 of androgen receptor (AR) ligand-binding domains (LBDs) in antagonistic mode, resulting in a reduced level of AR upon exposure. The in silico binding energies of 6:2 diPAP with both ER and AR were lower than 8:2 diPAP, explaining the observed greater in vivo estrogenic and antiandrogenic activities of 6:2 diPAP. This study provided the first line of evidences that diPAPs could display adverse effects on the endocrine functions of fish species.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping