Zebrafish developmental toxicity assay: A fishy solution to reproductive toxicity screening, or just a red herring?

Reprod Toxicol. 2011 Sep;32(2):213-9. doi: 10.1016/j.reprotox.2011.06.119. Epub 2011 Jun 21.

Abstract

The zebrafish embryotoxicity/teratogenicity assay is described as a useful alternative screening model to evaluate the effect of drugs on embryofoetal development. Fertilized eggs were exposed to different concentrations of 15 compounds with teratogenic (8) and non-teratogenic (7) potential until 96h post-fertilization when 28 morphological endpoints and the level of compound uptake was assessed. The majority of drugs testing positive in mammals was also positive in zebrafish (75% sensitivity), while a relative high number of false positives were noted (43% specificity). Compound uptake determination appears useful for clarifying classifications as teratogenic or potential overdose although assay sensitivity could be improved to 71% if the exposure threshold, previously suggested as ∼50ng/larvae, is reconsidered. The zebrafish assay shows some potential, though limited in its current form, as a screening tool for developmental toxicity within Janssen drug development. Further assay refinement with respect to endpoints and body burden threshold is required.

MeSH terms

  • Animals
  • Body Burden
  • Congenital Abnormalities / etiology
  • Dose-Response Relationship, Drug
  • Embryo, Nonmammalian / abnormalities
  • Embryo, Nonmammalian / drug effects*
  • Embryonic Development / drug effects*
  • Endpoint Determination
  • False Positive Reactions
  • Teratogens / pharmacokinetics
  • Teratogens / toxicity*
  • Toxicity Tests* / methods
  • Toxicity Tests* / standards
  • Toxicity Tests* / statistics & numerical data
  • Zebrafish / abnormalities
  • Zebrafish / embryology*

Substances

  • Teratogens