PUBLICATION

Commentary: catching a conserved mechanism of ethanol teratogenicity

Authors
Lovely, C.B., Eberhart, J.K.
ID
ZDB-PUB-140827-6
Date
2014
Source
Alcoholism, clinical and experimental research   38: 2160-3 (Other)
Registered Authors
Eberhart, Johann
Keywords
Fetal Alcohol Spectrum Disorder, Zebrafish
MeSH Terms
  • Animals
  • Fetal Alcohol Spectrum Disorders/etiology*
  • Neurotoxicity Syndromes/embryology*
PubMed
25156611 Full text @ Alcoholism Clin. Exp. Res.
Abstract
Due to its profound impact on human development, ethanol (EtOH) teratogenicity is a field of intense study. The complexity of variables that influence the outcomes of embryonic or prenatal EtOH exposure compels the use of animal models in which these variables can be isolated.
Numerous model systems have been used in these studies. The zebrafish is a powerful model system, which has seen a recent increase in usage for EtOH studies.
Those using zebrafish for alcohol studies often face 2 questions: (i) How physiologically relevant are the doses of EtOH administered to zebrafish embryos? and (ii) Will the mechanisms of EtOH teratogenesis be conserved to other model systems and human?
The current article by Flentke and colleagues () helps to shed important light on these questions and clearly demonstrates that the zebrafish will be a valuable model system with which to understand EtOH teratogenicity.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping