Wendel A
Z Gastroenterol. 1984 Jan;22(1):9-15.
Using the primary hepatotoxin paracetamol (acetaminophen) as a model it is shown in vivo in the mouse that the phase I metabolism of this agent causes a dose-dependent lipid peroxidation. This finding is extended to other xenobiotics activated in phase I and becomes manifest only if the glutathione redox systems as an endogenous defense system is paralyzed. The concept of lipid peroxidation being an early causal event in hepatocellular destruction was experimentally examined: Animals with alimentary selenium deficiency lacking glutathione peroxidase activity were much more susceptible to drug overdosage. Animals pretreated with liposomally entrapped reduced glutathione were totally resistant. Using the isolated perfused liver it is demonstrated that lipid peroxidation precedes cell disintegration. These animal data are discussed with respect to the biochemical parameters available for man. The results suggest an involvement of lipid peroxidation in certain acute chemical lesions, but do not justify to derive a general pathogenic concept based on lipid peroxidation.
以原发性肝毒素对乙酰氨基酚(扑热息痛)为模型,在小鼠体内研究表明,该药物的I相代谢会导致剂量依赖性脂质过氧化。这一发现扩展到其他在I相被激活的外源性物质,并且只有当作为内源性防御系统的谷胱甘肽氧化还原系统瘫痪时才会显现出来。脂质过氧化是肝细胞破坏早期因果事件的概念通过实验进行了检验:缺乏谷胱甘肽过氧化物酶活性的膳食硒缺乏动物对药物过量更敏感。用脂质体包裹的还原型谷胱甘肽预处理的动物则完全具有抗性。利用离体灌注肝脏证明,脂质过氧化先于细胞解体。结合人类可用的生化参数对这些动物数据进行了讨论。结果表明脂质过氧化参与了某些急性化学损伤,但并不足以得出基于脂质过氧化的一般致病概念。