The mechanism of prevention of paracetamol-induced hepatotoxicity by 3,5-dialkyl substitution: The roles of glutathione depletion and oxidative stress
Recently, we have reported that 3,5-dialkyl substitution of paracetamol, in contrast to 3-monoalkyl substitution, prevented the paracetamol-induced toxicity in freshly isolated rat hepatocytes without having any effect on its cytochrome P-450 mediated bioactivation to reactive N-acetyl- p-benzoquino...
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Veröffentlicht in: | Biochemical pharmacology 1987-07, Vol.36 (13), p.2065-2070 |
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