PUBLICATION

Testing estrogenicity of known and novel (xeno-)estrogens in the MolDarT using developing zebrafish (Danio rerio)

Authors
Muncke, J., Junghans, M., and Eggen, R.I.
ID
ZDB-PUB-070330-15
Date
2007
Source
Environmental toxicology   22(2): 185-193 (Journal)
Registered Authors
Keywords
atrazine, cyproconazol, estradiol, ethinylestradiol, nonylphenol, developing zebrafish, MolDarT, ecotoxicology, YES, real-time PCR
MeSH Terms
  • Animals
  • Atrazine/toxicity
  • Benzhydryl Compounds
  • Biological Assay
  • Estrogens/toxicity*
  • Ethinyl Estradiol/toxicity
  • Fungicides, Industrial/toxicity
  • Herbicides/toxicity
  • Phenols/toxicity
  • Receptors, Estrogen/metabolism
  • Triazoles/toxicity
  • Vitellogenins/metabolism*
  • Zebrafish/embryology
  • Zebrafish/metabolism*
PubMed
17366571 Full text @ Env. Tox.
CTD
17366571
Abstract
The MolDarT is a novel short-term assay for testing mechanism-based molecular effects in developing zebrafish embryos. The objective of this study was to evaluate the inducibility of vitellogenin1 mRNA (Vtg1) by the estrogenically active compounds 17beta-Estradiol (E2), 17alpha-Ethinylestradiol (EE2), Nonylphenol (NP), Bisphenol A (BPA), Cyproconazol, and the suspected xeno-estrogen Atrazin in the MolDarT. Freshly fertilized zebrafish eggs were exposed semistatically for 120 h. Using reverse transcription real-time PCR, the relative abundance of Vtg1 was measured. For EE2 a dose-response relationship was established with EC50 = 60.7 ng/L (205 pM). Induction of Vtg1 was significant at concentrations of 84 pM EE2 (25 ng EE2/L) and above, 10 nM E2 (2.7 mug E2/L), 100 nM E2 (27 mug E2/L), 10 muM BPA (2280 mug BPA/L), and 15 muM BPA (3420 mug BPA/L). At NP concentrations of 0.75 muM (165 mug NP/L) and 1.5 muM (330 mug NP/L) Vtg1 was significantly down-regulated. Both atrazine and cyproconazol showed no effect on relative Vtg1 abundance. With this study we further characterize the MolDarT assay and show its applicability for effect screening of compounds.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping