Effect of deferrioxamine and diethyldithiocarbamate on paracetamol-induced hepato- and nephrotoxicity. The role of lipid peroxidation

✍ Scribed by Maged Younes; Christiane Sause; Claus-Peter Siegers; Robert Lemoine

• Publisher: John Wiley and Sons
• Year: 1988
• Tongue: English
• Weight: 513 KB
• Volume: 8
• Category: Article
• ISSN: 0260-437X
• DOI: 10.1002/jat.2550080407

✦ Synopsis

In mice subjected to glutathione depletion by pretreatment with phorone (diisopropylidene acetone, 200 mgl kg i.p. in 10 mlkg olive oil) paracetamol (acetaminophen, 300 mgkg p.0. in 10 ml/kg tylose 2 h later) led to a marked hepatotoxicity as evidenced by increased plasma activities of the liver-specific enzymes sorbitol dehydrogenase (SDH) and glutamate-pyruvate-transaminase (GPT) 3 and 24 h after treatment. Nephrotoxicity was also indicated at both timepoints by an increased creatinine concentration in plasma, while neither the urine volume nor Its content in y-glutamyl transpeptitase over 20 h were affected. Hepato-and nephrotoxicity were also assessed histomorphologically . In vivo lipid peroxidation (LPO), as measured by ethane exhalation over 3 h, was clearly enhanced by paracetamol. Malondialdehyde content was increased and glutathione concentration diminished in the liver, but not in the kidney. Diethyldithiocarbamate (DTC, 200 mglkg i.p.) or deferrioxamine (DFO, 500 mg/kg i.p.) both given 30 min before PA, inhibited in vivo LPO. However, only DTC was capable of antagonizing the hepato-and nephrotoxic effects of paracetamol, while DFO only delayed the onset of nephrotoxicity but left the hepatotoxicity unaffected. Both agents inhibited the rise in hepatic malondialdehyde-content, but only DTC prevented paracetamol-induced glutathione depletion. These results indicate that LPO is not mainly responsible for paracetamol toxicity towards liver or kidney.