PUBLICATION

Toxicant induced behavioural aberrations in larval zebrafish are dependent on minor methodological alterations

Authors
Fraser, T.W.K., Khezri, A., Jusdado, J.G.H., Lewandowska-Sabat, A.M., Henry, T., Ropstad, E.
ID
ZDB-PUB-170523-9
Date
2017
Source
Toxicology letters   276: 62-68 (Journal)
Registered Authors
Henry, Theodore B.
Keywords
bisphenol A, brain, endocrine disruption, locomotion, neurotoxicology, tetrabromobisphenol A
MeSH Terms
  • Animals
  • Behavior, Animal/drug effects*
  • Benzhydryl Compounds/toxicity*
  • Biological Assay*
  • Dose-Response Relationship, Drug
  • Larva/drug effects
  • Locomotion/drug effects*
  • Phenols/toxicity*
  • Photoperiod
  • Polybrominated Biphenyls/toxicity*
  • Reproducibility of Results
  • Risk Assessment
  • Time Factors
  • Toxicity Tests/methods*
  • Zebrafish/embryology*
PubMed
28529144 Full text @ Toxicol. Lett.
Abstract
Alterations in zebrafish motility are used to identify neurotoxic compounds, but few have reported how methodology may affect results. To investigate this, we exposed embryos to bisphenol A (BPA) or tetrabromobisphenol A (TBBPA) before assessing larval motility. Embryos were maintained on a day/night cycle (DN) or in constant darkness, were reared in 96 or 24 well plates (BPA only), and behavioural tests were carried out at 96, 100, or 118 (BPA only) hours post fertilisation (hpf). We found that the prior photo-regime, larval age, and/or arena size influence behavioural outcomes in response to toxicant exposure. For example, methodology determined whether 10μM BPA induced hyperactivity, hypoactivity, or had no behavioural effect. Furthermore, the minimum effect concentration was not consistent between different methodologies. Finally, we observed a mechanism previously used to explain hyperactivity following BPA exposure does not appear to explain the hypoactivity observed following minor alterations in methodology. Therefore, we demonstrate how methodology can have notable implications on dose responses and behavioural outcomes in larval zebrafish motility following identical chemical exposures. As such, our results have significant consequences for human and environmental risk assessment.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping