PUBLICATION

Using Zebrafish for Investigating the Molecular Mechanisms of Drug-Induced Cardiotoxicity

Authors
Zakaria, Z.Z., Benslimane, F.M., Nasrallah, G.K., Shurbaji, S., Younes, N.N., Mraiche, F., Da'as, S.I., Yalcin, H.C.
ID
ZDB-PUB-181027-8
Date
2018
Source
BioMed Research International   2018: 1642684 (Review)
Registered Authors
Da'as, Sahar, Nasrallah, Gheyath
Keywords
none
MeSH Terms
  • Animals
  • Cardiotoxicity/etiology*
  • Drug-Related Side Effects and Adverse Reactions/etiology*
  • Hemodynamics/physiology
  • Humans
  • Pharmaceutical Preparations/administration & dosage*
  • Zebrafish/physiology*
PubMed
30363733 Full text @ Biomed Res. Int.
Abstract
Over the last decade, the zebrafish (Danio rerio) has emerged as a model organism for cardiovascular research. Zebrafish have several advantages over mammalian models. For instance, the experimental cost of using zebrafish is comparatively low; the embryos are transparent, develop externally, and have high fecundity making them suitable for large-scale genetic screening. More recently, zebrafish embryos have been used for the screening of a variety of toxic agents, particularly for cardiotoxicity testing. Zebrafish has been shown to exhibit physiological responses that are similar to mammals after exposure to medicinal drugs including xenobiotics, hormones, cancer drugs, and also environmental pollutants, including pesticides and heavy metals. In this review, we provided a summary for recent studies that have used zebrafish to investigate the molecular mechanisms of drug-induced cardiotoxicity. More specifically, we focused on the techniques that were exploited by us and others for cardiovascular toxicity assessment and described several microscopic imaging and analysis protocols that are being used for the estimation of a variety of cardiac hemodynamic parameters.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping