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The possibility of minimizing iron intake or removing iron may prove beneficial for the treatment of liver injury and it is clearly an area that deserves further research ( For investigating the pathogenesis and treatment of APAP-induced hepatotoxicity, the role of iron was evaluated as was whether PA played a role in the treatment of APAP-induced hepatotoxicity in light of its importance as an iron chelator and its ability to block the generation of iron-driven hydroxyl radicals as well as the suppression of lipid peroxidation ( The serum iron could reflect hepatic iron accumulation, which is considered an important factor in the progression of liver fibrosis ( On exposure to a toxic dose of APAP, ferrous iron is released into the cytosol from the ruptured lysosomes ( The current results showed that APAP treatment induced a statistically significant increase in MDA and a decrease in GSH levels compared to the control group, while PA produced a significant improvement in oxidative stress by decreasing the MDA level and increasing the GSH level compared to the APAP group

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