PUBLICATION

In vivo zebrafish assays for toxicity testing

Authors
Parng, C.
ID
ZDB-PUB-050201-10
Date
2005
Source
Curr. Opin. Drug Discov. Devel.   8(1): 100-106 (Review)
Registered Authors
Parng, Chuenlei
Keywords
none
MeSH Terms
  • Animals
  • Carcinogens/toxicity
  • Cardiovascular Diseases/chemically induced
  • Immune System/drug effects
  • Labyrinth Diseases/chemically induced
  • Neurotoxicity Syndromes/pathology
  • Toxicogenetics
  • Toxicology/methods*
  • Xenobiotics/metabolism
  • Zebrafish/physiology*
PubMed
15679177
Abstract
Toxicity, due to complications of in vivo adsorption, distribution, metabolism and excretion (ADME), is a major cause of failure during drug development; many drugs shown to be safe in cell culture prove toxic in animal studies. Effective in vivo toxicity screening early in the development process can reduce the number of compounds that progress to laborious and costly late-stage animal testing. The transparent zebrafish provides accessibility to internal organs, tissues and even cells, and has emerged as an invaluable model organism for toxicity testing and drug discovery. Straightforward in vivo zebrafish assays can serve as an intermediate step between cell-based and mammalian testing, thus streamlining the drug development time-line.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping