PUBLICATION
Long-term exposure to bisphenol S damages the visual system and reduces the tracking capability of male zebrafish (Danio rerio)
- Authors
- Liu, W., Zhang, X., Wei, P., Tian, H., Wang, W., Ru, S.
- ID
- ZDB-PUB-170912-3
- Date
- 2017
- Source
- Journal of applied toxicology : JAT 38(2): 248-258 (Journal)
- Registered Authors
- Keywords
- bps, opsin genes, retinal structure, visual behaviors, zebrafish
- MeSH Terms
-
- Apoptosis/drug effects
- Apoptosis/genetics
- Behavior, Animal/drug effects*
- Opsins/genetics
- Animals
- PubMed
- 28892180 Full text @ J. Appl. Toxicol.
- CTD
- 28892180
Abstract
Bisphenol S (BPS) is widely detected in aquatic environments and in human bodies. BPS has reproductive and thyroid disrupting effects, but its effect on the visual system remains unknown. In the present study, zebrafish embryos were exposed to BPS at concentrations of 1, 10, 100 and 1000 μg l-1 until 120 days post-fertilization in a semistatic system, and the effect of BPS on the visual behavior was examined using the optokinetic response and the optomotor response tests in male zebrafish. The retinal histology, mRNA expression of photoreceptor opsin genes (zfrho, zfblue, zfgr1, zfred and zfuv) and apoptosis-related genes (bax and bcl-2) were also assessed. Long-term BPS exposure decreased the tracking capability of male zebrafish, consistent with structural damage to the retina. BPS induced different amounts of vacuoles in the retinal pigment epithelium, and 1000 μg l-1 BPS exposure decreased the length of the inner plexiform layer, ganglion cell layer and retina, and induced an irregular arrangement of photoreceptor cells. The expression levels of the opsin genes (zfred, zfgr1 and zfrho) were significantly elevated, indicating an enhanced spectral sensitivity to red, green and dim light to compensate for the reduction of the optomotor response. Together, the results showed for the first time that long-term exposure to BPS damaged the structure of male zebrafish retina and reduced their tracking capability.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping