Suntres Z E, Lui E M
Department of Pharmacology and Toxicology, University of Western Ontario, London.
J Pharmacol Exp Ther. 1991 Sep;258(3):797-806.
This study was concerned with the role of Cu and Cu-MT (metallothionein) in oxidative stress. Because hepatic Cu and Cu-MT concentrations are known to be high in the 3-day-old guinea pigs but decline to low adult levels by 7 days of life, the hepatotoxicity of ferric nitrilotriacetate (FeNTA) in the developing guinea pig was used as the experimental model in the present study. Results of this study showed that the hepatotoxic response to FeNTA (3.5 mg Fe /kg i.p.) as measured by elevation in serum aspartate aminotransferase activity, increase in lipid peroxidation, decrease in reduced glutathione/oxidized glutathione ratio and histopathological changes was higher in 3-day-old than in 7-day-old and adult guinea pigs. Furthermore, pretreatment of 7-day-old guinea pigs with cupric sulfate (0.5 mg Cu++/kg i.p.) increased hepatic Cu and Cu-MT levels and enhanced susceptibility to FeNTA. FeNTA treatment resulted in the oxidation of MT thiolates and reduction in the metal binding capacity and Cu content of MT in the 3-day-old and Cu-pretreated 7-day-old animals, providing evidence for the interaction between Cu-MT and cellular oxidants. In vitro study with FeNTA and hepatic microsomes revealed no age-related differences in microsomal lipid peroxidation; however, this parameter was stimulated in the presence of control or heat-treated cytosols isolated from 3-day-old but not those of 7-day-old animals. These observations were consistent with the involvement of Cu-MT, a heat-stable metalloprotein, in the sensitization of hepatic tissues to oxidative injury in the 3-day-old animal. Moreover, in vitro study involving the use of D-penicillamine, a Cu chelating agent, showed that the sensitization effect of Cu-MT was mediated by Cu ions. The results of this study suggest that Cu-MT may have a prooxidative property and tissues with high Cu-MT levels may be particularly susceptible to oxidative stress.
本研究关注铜及铜-金属硫蛋白(MT)在氧化应激中的作用。由于已知3日龄豚鼠肝脏中的铜和铜-金属硫蛋白浓度较高,但在出生7天时会降至成年时的低水平,因此本研究将发育中的豚鼠对次氮基三乙酸铁(FeNTA)的肝毒性用作实验模型。本研究结果表明,以血清天冬氨酸转氨酶活性升高、脂质过氧化增加、还原型谷胱甘肽/氧化型谷胱甘肽比值降低以及组织病理学变化来衡量,3日龄豚鼠对FeNTA(3.5mg铁/千克腹腔注射)的肝毒性反应高于7日龄和成年豚鼠。此外,用硫酸铜(0.5mg铜离子/千克腹腔注射)对7日龄豚鼠进行预处理会增加肝脏中的铜和铜-金属硫蛋白水平,并增强对FeNTA的易感性。FeNTA处理导致3日龄和经铜预处理的7日龄动物中MT硫醇盐的氧化以及MT的金属结合能力和铜含量的降低,这为铜-金属硫蛋白与细胞氧化剂之间的相互作用提供了证据。用FeNTA和肝微粒体进行的体外研究表明,微粒体脂质过氧化不存在年龄相关差异;然而,在存在从3日龄动物分离的对照或热处理细胞溶质的情况下,该参数会受到刺激,而7日龄动物的细胞溶质则不会。这些观察结果与热稳定金属蛋白铜-金属硫蛋白参与3日龄动物肝脏组织对氧化损伤的致敏作用一致。此外,涉及使用铜螯合剂D-青霉胺的体外研究表明,铜-金属硫蛋白的致敏作用是由铜离子介导的。本研究结果表明,铜-金属硫蛋白可能具有促氧化特性,铜-金属硫蛋白水平高的组织可能对氧化应激特别敏感。