Department of Chemistry, Faculty of Science, University of Novi Sad, Novi Sad, Serbia.
Molecules. 2009 Nov 10;14(11):4505-16. doi: 10.3390/molecules14114505.
The aim of this work was to investigate the effect on antioxidant potential of some commonly used drugs (morphine, tramadol, bromocriptine, haloperidol and azithromycin) on immobilization stress (IS) combined with cold restraint stress (CRS) in the rat. After the drug treatment the animals were kept immobilized in the cold chamber at 4+/-0.3 degrees C for 3 hours and then decapitaed and the livers were extracted. The following parameters were determined in the liver homogenate: content of reduced glutathione, activities of catalase, xanthine oxidase, glutathione reductase, glutathione peroxidase, peroxidase, and lipid peroxidation intensity. A battery of biochemical assays was used and the resulting data were statistically analyzed. Combined stress exhibited a prooxidative action (increased catalase activity, lowered content of reduced glutathione). Significantly enhanced catalase activity that was observed in all groups compared to the control indicates that the primary reactive oxygen species (ROS) metabolite is hydrogen peroxide, which decomposes very rapidly (very high catalase activity), thus hindering formation of OH radicals as the most toxic ROS. None of the tested drugs showed a protective effect on combined IS and CRS. The intensity of lipid peroxidation did not change either in the combined stress or under additional influence of the drugs. Probably, under our experimental conditions, the time was not sufficiently long to observe damage of lipid membrane by ROS.
这项工作的目的是研究一些常用药物(吗啡、曲马多、溴隐亭、氟哌啶醇和阿奇霉素)对固定应激(IS)与冷束缚应激(CRS)联合作用于大鼠时的抗氧化潜力的影响。药物治疗后,动物在 4+/-0.3 摄氏度的冷室中固定 3 小时,然后断头并提取肝脏。在肝匀浆中测定以下参数:还原型谷胱甘肽含量、过氧化氢酶、黄嘌呤氧化酶、谷胱甘肽还原酶、谷胱甘肽过氧化物酶、过氧化物酶和脂质过氧化强度。采用一系列生化测定法,并对所得数据进行统计学分析。联合应激表现出促氧化作用(过氧化氢酶活性增加,还原型谷胱甘肽含量降低)。与对照组相比,所有组的过氧化氢酶活性均显著增强,表明主要的活性氧(ROS)代谢物是过氧化氢,它分解得非常快(过氧化氢酶活性非常高),从而阻止了 OH 自由基的形成,OH 自由基是最具毒性的 ROS。测试的药物均未显示对联合 IS 和 CRS 有保护作用。在联合应激或药物额外影响下,脂质过氧化的强度也没有变化。可能在我们的实验条件下,时间不够长,还不足以观察到 ROS 对脂质膜的损伤。