Yang C M, Carlson G P
Department of Pharmacology and Toxicology, School of Pharmacy and Pharmacal Sciences, Purdue University, West Lafayette, IN 47907.
Biochem Pharmacol. 1991;41(6-7):923-9. doi: 10.1016/0006-2952(91)90197-d.
The ability of ethanol to alter glutathione (GSH) conjugation and its dependence upon duration of administration were investigated in rats in correlation with lipid peroxidation and the induction of microsomal enzymes. Significant decreases in hepatic GSH and glutathione-S-transferase (GST) activity in both liver and lung were found in rats treated acutely with ethanol (4 g/kg body weight 6 hr prior to killing). These decreases were accompanied by an increased loss of both GSH and GST into the plasma and increased hepatic lipid peroxidation. On the other hand, there was a dose-dependent increase in hepatic GSH after chronic administration of ethanol in drinking water (5 and 10%) for 3 weeks. This increase in hepatic GSH may be due to increased synthesis of GSH in the liver. No significant induction of GST by chronic ethanol treatment was observed in either organ. Ethanol was compared with the well-known inducers phenobarbital and beta-naphthoflavone. Although there was some evidence of increases in lipid peroxidation and/or microsomal enzyme activity with the inducers, no simple link between these increases and the induction of GST activity was identified.
研究了乙醇改变谷胱甘肽(GSH)结合作用的能力及其对给药持续时间的依赖性,并将其与脂质过氧化和微粒体酶的诱导作用相关联,在大鼠中进行了研究。在用乙醇急性处理的大鼠(处死前6小时给予4克/千克体重)中,发现肝脏和肺中的肝GSH和谷胱甘肽-S-转移酶(GST)活性显著降低。这些降低伴随着GSH和GST向血浆中的损失增加以及肝脂质过氧化增加。另一方面,在饮用水中慢性给予乙醇(5%和10%)3周后,肝脏GSH呈剂量依赖性增加。肝脏GSH的这种增加可能是由于肝脏中GSH合成增加所致。在任一器官中,均未观察到慢性乙醇处理对GST有显著诱导作用。将乙醇与著名的诱导剂苯巴比妥和β-萘黄酮进行了比较。尽管有一些证据表明诱导剂会导致脂质过氧化和/或微粒体酶活性增加,但未发现这些增加与GST活性诱导之间存在简单联系。