PUBLICATION
Development of a screening assay to identify teratogenic and embryotoxic chemicals using the zebrafish embryo
- Authors
- Selderslaghs, I.W., Van Rompay, A.R., De Coen, W., and Witters, H.E.
- ID
- ZDB-PUB-090526-3
- Date
- 2009
- Source
- Reproductive toxicology (Elmsford, N.Y.) 28(3): 308-320 (Journal)
- Registered Authors
- Witters, Hilda
- Keywords
- Zebrafish embryo, Screening, Chemicals, Teratogenicity, Embryotoxicity
- MeSH Terms
-
- Abnormalities, Drug-Induced*
- Animal Testing Alternatives*
- Animals
- Bone and Bones/abnormalities
- Bone and Bones/drug effects
- Dose-Response Relationship, Drug
- Embryo, Nonmammalian/drug effects*
- Embryonic Development/drug effects*
- Female
- In Vitro Techniques
- Life Cycle Stages/drug effects
- Male
- Predictive Value of Tests
- Reproducibility of Results
- Risk Assessment
- Teratogens/classification
- Teratogens/toxicity*
- Toxicity Tests/methods
- Xenobiotics/classification
- Xenobiotics/toxicity*
- Zebrafish*
- PubMed
- 19447169 Full text @ Reprod. Toxicol.
Citation
Selderslaghs, I.W., Van Rompay, A.R., De Coen, W., and Witters, H.E. (2009) Development of a screening assay to identify teratogenic and embryotoxic chemicals using the zebrafish embryo. Reproductive toxicology (Elmsford, N.Y.). 28(3):308-320.
Abstract
We developed and optimized a screening procedure, in which zebrafish embryos were explored as a model for the evaluation of the specific embryotoxic and teratogenic potential of chemicals. A selection of known positive (retinoic acid, valproic acid, caffeine, lithium chloride) and negative (glucose, saccharin) compounds for developmental toxicity were used to evaluate this method. We exposed embryos and evaluated embryotoxicity and morphological characteristics of the embryos at 24, 48, 72 and 144hours post fertilization. After evaluation of the induced effects, concentration-response curves were created for both embryotoxicity and teratogenic effects. Values for teratogenic indices (TI) were calculated as the ratio LC(50)/EC(50). The results obtained were compared to existing data from studies with laboratory animals and humans. We demonstrated that our classification of the compounds, based on TI values, allows to distinguish teratogens from non-teratogens and supports the application of zebrafish embryos as an alternative method for developmental toxicity studies to predict effects in mammals.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping