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    2,3,7,8-Tetrachlorodibenzo-p-Dioxin induced Oxygen Activation associated with Cell Respiration.
        
        Free Radical Biol. Med. 6, 369-374 (1989)
    
    
    
	    We have investigated the influence of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) on bioenergetic functions of isolated heart-mitochondria. Electron transfer and energy conservation activities were found to be decreased in the presence of very amounts of the polychlorinated biphenyl compound (1.5 nmol/mg mitochondrial protein). The effect was greatest when substrates for complex I were used. In this case coupling of oxidative phosphorylation to respiration was drastically diminished, essentially at the expense of state 3 respiration, and P/O values were found around 2 instead of 3. Succinate-related energy conservation remained practically unaffected in the presence of TCDD, suggesting an interference of the toxic compound at coupling site I. SOD plus catalase found to protect energy-linked respiration from the effect of dioxin indicating the involvement of superoxide radicals and H2O2 in the development of the observed phenomena. The present contribution provides experimental evidence on the formation of these oxygen species in the presence of TCDD. Furthermore, the site of action of TCDD is demonstrated and discussedd in relation to the oxygen radical formation observed.
	
	
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        Publication type
        Article: Journal article
    
 
    
        Document type
        Scientific Article
    
 
     
    
    
        Keywords
        TCDD; Inhibition of mitochondrial respiration; Oxygen activation; Energy conservation
    
 
     
    
    
        Language
        english
    
 
    
        Publication Year
        1989
    
 
     
    
        HGF-reported in Year
        0
    
 
    
    
        ISSN (print) / ISBN
        0891-5849
    
 
    
        e-ISSN
        1873-4596
    
 
    
     
     
	     
	 
	 
     
	
    
        Quellenangaben
        
	    Volume: 6,  
	    Issue: 4,  
	    Pages: 369-374 
	    
	    
	
    
 
    
         
        
            Publisher
            Elsevier
        
 
        
            Publishing Place
            New York, NY
        
 
	
         
         
         
         
         
	
         
         
         
    
         
         
         
         
         
         
         
    
        Reviewing status
        Peer reviewed
    
 
     
     
     
     
     
     	
    
    
        WOS ID
        WOS:A1989T816600005
    
    
        Erfassungsdatum
        1989-12-31