PUBLICATION
            Glutathione transferase pi class 2 (GSTp2) protects against the cardiac deformities caused by exposure to PAHs but not PCB-126 in zebrafish embryos
- Authors
- Garner, L.V., and Di Giulio, R.T.
- ID
- ZDB-PUB-120125-43
- Date
- 2012
- Source
- Comparative biochemistry and physiology. Toxicology & pharmacology : CBP 155(4): 573-579 (Journal)
- Registered Authors
- Di Giulio, Richard T.
- Keywords
- glutathione transferase, morpholino, polycyclic aromatic hydrocarbons, polychlorinated biphenyls, zebrafish, cardiotoxicity
- MeSH Terms
- 
    
        
        
            
                - Drug Therapy, Combination
- Zebrafish
- Gene Expression Regulation, Developmental/drug effects
- Animals
- Heart Defects, Congenital*/chemically induced
- Heart Defects, Congenital*/metabolism
- Heart Defects, Congenital*/prevention & control
- Embryo, Nonmammalian/drug effects*
- Embryo, Nonmammalian/enzymology
- Drug Synergism
- Polychlorinated Biphenyls/toxicity*
- Estrogen Antagonists/toxicity*
- Polycyclic Aromatic Hydrocarbons/classification
- Polycyclic Aromatic Hydrocarbons/toxicity*
- Embryonic Development/drug effects*
- Morpholinos/administration & dosage
- Morpholinos/genetics
- Gene Silencing/drug effects
- Gene Silencing/physiology
- Glutathione S-Transferase pi/genetics
- Glutathione S-Transferase pi/metabolism*
- Gene Knockdown Techniques
 
- PubMed
- 22269188 Full text @ Comp. Biochem. Physiol. C Toxicol. Pharmacol.
- CTD
- 22269188
            Citation
        
        
            Garner, L.V., and Di Giulio, R.T. (2012) Glutathione transferase pi class 2 (GSTp2) protects against the cardiac deformities caused by exposure to PAHs but not PCB-126 in zebrafish embryos. Comparative biochemistry and physiology. Toxicology & pharmacology : CBP. 155(4):573-579.
        
    
                
                    
                        Abstract
                    
                    
                
                
            
        
        
    
        
            
            
 
    
    
        
    
    
    
        
                Glutathione transferases (GSTs) are phase II enzymes that detoxify a wide range of toxicants and reactive intermediates. One such class of toxicants is the ubiquitous polycyclic aromatic hydrocarbons (PAHs). Certain PAHs are known to cause developmental cardiac toxicity in fish. Herein, we explored the role of GST pi class 2 (GSTp2) in PAH- and PCB-induced cardiac toxicity in zebrafish (Danio rerio) embryos. We measured expression of GSTp2 in embryos exposed to individual and co-exposures of the PAHs benzo[k]fluoranthene (BkF), benzo[a]pyrene (BaP), and fluoranthene (FL) as well as 3,32,4,42,5-pentachlorobiphenyl (PCB-126). GSTp2 mRNA expression was induced by exposure to BkF, BaP, PCB-126, and BaP + FL and BkF + FL co-exposure. A splice junction morpholino was then used to knockdown GSTp2 in developing zebrafish. GSTp2 knockdown exacerbated the toxicity caused by co-exposures to BkF + FL and BaP + FL. However, GSTp2 knockdown did not affect PCB-126 toxicity. These results further suggest that pi class GSTs serve a protective function against the synergistic toxicity caused by PAHs in developing zebrafish.
            
    
        
        
    
    
    
                
                    
                        Genes / Markers
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Expression
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Phenotype
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mutations / Transgenics
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Human Disease / Model
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Sequence Targeting Reagents
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Fish
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Orthology
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Engineered Foreign Genes
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    
                
                    
                        Mapping
                    
                    
                
                
            
        
        
    
        
            
            
        
        
    
    
    