Junqueira V B, Barros S B, Simizu K, Fernández V, Carrión Y, Pimentel R, Azzalis L A, Videla L A
Departamento de Bioquímica, Universidade de São Paulo, Brasil.
Toxicol Lett. 1993 Aug;69(2):211-6. doi: 10.1016/0378-4274(93)90106-8.
The administration of lindane (60 mg/kg) to fed rats diminished the content of hepatic glutathione (GSH) 4 h after treatment, which was recovered at 24 h. At these experimental times, the activities of glutathione peroxidase, glutathione reductase, glutathione-S-transferases and gamma-glutamyltransferase in the liver of lindane-treated rats and control animals were comparable. Liver GSH turnover, measured after a pulse of [35S]cysteine, was enhanced by 69% (P < 0.05) in lindane-treated rats 24 h after intoxication compared to controls, with a 63% (P < 0.05) increase in the estimated rate of GSH synthesis. It is concluded that lindane enhances GSH synthesis in rat liver 24 h after treatment as a consequence of the decrement in its content observed at early times of intoxication (4 h), thus allowing the recovery of the normal level of hepatic GSH.
给喂食后的大鼠施用林丹(60毫克/千克),处理后4小时肝脏谷胱甘肽(GSH)含量降低,24小时后恢复。在这些实验时间点,林丹处理组大鼠和对照组动物肝脏中的谷胱甘肽过氧化物酶、谷胱甘肽还原酶、谷胱甘肽-S-转移酶和γ-谷氨酰转移酶的活性相当。与对照组相比,中毒24小时后,经[35S]半胱氨酸脉冲处理后测定的林丹处理组大鼠肝脏GSH周转率提高了69%(P<0.05),GSH合成估计速率增加了63%(P<0.05)。结论是,由于中毒早期(4小时)观察到林丹含量下降,处理24小时后林丹可增强大鼠肝脏GSH的合成,从而使肝脏GSH恢复到正常水平。