Arthur M J, Bentley I S, Tanner A R, Saunders P K, Millward-Sadler G H, Wright R
Gastroenterology. 1985 Nov;89(5):1114-22. doi: 10.1016/0016-5085(85)90218-5.
We have investigated the possible protective effect of superoxide dismutase and allopurinol in a rat model of mild and severe hepatic necrosis produced by Corynebacterium parvum with or without endotoxin. Histology showed a sinusoidal mononuclear cell infiltrate with multiple granulomata but variable degrees of hepatic necrosis. In the severe hepatic injury model there was a reduction in mortality, associated with a decrease in histologic and biochemical evidence of hepatic necrosis, after treatment with superoxide dismutase. This protective effect was not demonstrated with partially heat-inactivated superoxide dismutase. In the mild hepatic injury model similar trends in reduction of serum levels of hepatic enzymes were observed after treatment with both superoxide dismutase and allopurinol. These results indicate that oxygen-derived free radicals may play an important role in the pathogenesis of hepatic injury in the rat.
我们研究了超氧化物歧化酶和别嘌呤醇在由小棒状杆菌伴或不伴内毒素所导致的轻、重度肝坏死大鼠模型中的可能保护作用。组织学显示有窦状单核细胞浸润及多个肉芽肿,但肝坏死程度各异。在重度肝损伤模型中,超氧化物歧化酶治疗后死亡率降低,同时肝坏死的组织学和生化证据减少。部分热灭活的超氧化物歧化酶未显示出这种保护作用。在轻度肝损伤模型中,超氧化物歧化酶和别嘌呤醇治疗后均观察到肝酶血清水平降低的类似趋势。这些结果表明,氧衍生的自由基可能在大鼠肝损伤的发病机制中起重要作用。