Hassing J M, Rosenberg H, Stohs S J
Res Commun Chem Pathol Pharmacol. 1979 Jul;25(1):3-11.
The time course of acetaminophen-induced hepatic glutathione depletion and recovery in control and streptozotocin-diabetic female rats was investigated. Initial hepatic glutathione levels were significantly higher in control animals. After a 1 g/kg intraperitoneal dose of acetaminophen, maximum depletion of reduced glutathione (GSH) occurred within 2 h in diabetics and began to increase thereafter, while maximum GSH depletion occurred at approx. 4 h in controls and did not begin to return to normal until after 12 h. The time course for changes in hepatic oxidized glutathione (GSSG) after acetaminophen administration followed that for GSH in both control and diabetic rats. Diurnal variations in hepatic glutathione levels do occur, but these variations can not explain the changes which occur following acetaminophen administration or the differences observed between control and diabetic rats. Diabetic rats are more susceptible to the glutathione depleting effects of high-dose acetaminophen, suggesting that the diabetic may be less able to detoxify drugs and foreign chemicals.
研究了对乙酰氨基酚诱导的对照雌性大鼠和链脲佐菌素诱导的糖尿病雌性大鼠肝脏谷胱甘肽耗竭及恢复的时间进程。对照动物的初始肝脏谷胱甘肽水平显著更高。腹腔注射1 g/kg对乙酰氨基酚后,糖尿病大鼠在2小时内出现还原型谷胱甘肽(GSH)的最大耗竭,此后开始增加,而对照大鼠在约4小时出现GSH最大耗竭,直到12小时后才开始恢复正常。对乙酰氨基酚给药后肝脏氧化型谷胱甘肽(GSSG)变化的时间进程在对照大鼠和糖尿病大鼠中均与GSH的情况一致。肝脏谷胱甘肽水平确实存在昼夜变化,但这些变化无法解释对乙酰氨基酚给药后发生的变化或对照大鼠与糖尿病大鼠之间观察到的差异。糖尿病大鼠对高剂量对乙酰氨基酚的谷胱甘肽耗竭作用更敏感,这表明糖尿病大鼠可能对药物和外来化学物质的解毒能力较低。