Nelson E B, Montes M, Goldstein M
Toxicology. 1980;17(1):73-81. doi: 10.1016/0300-483x(80)90029-3.
Metyrapone tartrate, 400 mg/kg i.p. raised the LD50 for acetaminophen from 340 mg/kg i.p. to 540 mg/kg i.p. in fasting male Swiss white mice. The minimum protective dose of metyrapone was 200 mg/kg. Metyrapone was effective in preventing death when given up to 2 h after acetaminophen administration. The LD50 for metyrapone tartrate was 760 mg/kg i.p. Metyrapone decreased or prevented acetaminophen induced hepatic damage measured either by histology or plasma glutamate pyruvate transaminase activity. Metyrapone tartrate, 400 mg/kg i.p., inhibited the severe liver glutathione depletion seen with acetaminophen alone. It is proposed that metyrapone protects mice from acetaminophen induced liver toxicity and death by inhibiting the oxidation of acetaminophen to a toxic intermediate.
酒石酸美替拉酮,腹腔注射400毫克/千克,可使禁食的雄性瑞士小白鼠对乙酰氨基酚的半数致死量从腹腔注射340毫克/千克提高到540毫克/千克。美替拉酮的最小保护剂量为200毫克/千克。在乙酰氨基酚给药后2小时内给予美替拉酮可有效预防死亡。酒石酸美替拉酮的腹腔注射半数致死量为760毫克/千克。美替拉酮可减轻或预防通过组织学或血浆谷丙转氨酶活性测定的乙酰氨基酚诱导的肝损伤。腹腔注射400毫克/千克的酒石酸美替拉酮可抑制单独使用乙酰氨基酚时出现的严重肝脏谷胱甘肽耗竭。有人提出,美替拉酮通过抑制乙酰氨基酚氧化为有毒中间体来保护小鼠免受乙酰氨基酚诱导的肝毒性和死亡。