“ APAP administration induces hepatotoxicity, lipid peroxidation, and glutathione (GSH) depletion, and these were markedly suppressed by the ferroptosis-specific inhibitor Ferrostatin-1 (Fer-1), the iron chelator deferoxamine, and α-tocopherol ( vitamin E ), indicating that ferroptosis in hepatocytes contributes to the development of APAP-induced hepatotoxicity.”