Miura Y, Utsumi H, Hamada A
Department of Health Chemistry, School of Pharmaceutical Sciences, Showa University, Tokyo, Japan.
Arch Biochem Biophys. 1993 Jan;300(1):148-56. doi: 10.1006/abbi.1993.1021.
Inhibition of lipid peroxidation by nitroxide radicals in rat liver microsomes was studied using several nitroxide compounds which have various lipophilicities. Addition of NADPH to microsomes in an oxygen atmosphere induced lipid peroxidation as indicated by the increase of thiobarbituric acid (TBA)-reactive substances, hydroperoxide, conjugated diene, and oxygen consumption. Lipid peroxidation was inhibited by nitroxides located in both water phase and membrane. Oxygen consumption and the generation of active oxygens were inhibited by water-soluble nitroxides but not by intramembranous ones. Intramembranous nitroxides significantly prevented the production of conjugated dienes and lipid hydroperoxides. The facts suggest that water-soluble nitroxides interfere with the generation of active oxygens as preventive antioxidants, while intramembranous nitroxides inhibit the formation of lipid alkyl radical as chain-breaking antioxidants. The intensity of ESR signals due to intramembranous nitroxide radicals remained constant during the inhibition reaction of lipid peroxidation, suggesting that the prevention of lipid peroxidation is coupled with the reversible redox reaction between nitroxides and the reduced nitroxides in microsomes. The reduced forms of nitroxides, which were prepared by the reduction of intramembranous nitroxides, also inhibited the generation of TBA-reactive substances as well as the parent nitroxide. These facts indicate that either intramembranous nitroxide radicals or their reduced forms, "hydroxylamines," may be useful lipophilic antioxidants.
使用几种具有不同亲脂性的氮氧化物化合物,研究了氮氧化物自由基对大鼠肝微粒体脂质过氧化的抑制作用。在氧气氛围中向微粒体中添加NADPH会诱导脂质过氧化,这可通过硫代巴比妥酸(TBA)反应性物质、氢过氧化物、共轭二烯和耗氧量的增加来表明。水相和膜中的氮氧化物均可抑制脂质过氧化。水溶性氮氧化物可抑制耗氧量和活性氧的生成,但膜内氮氧化物则不能。膜内氮氧化物可显著阻止共轭二烯和脂质氢过氧化物的产生。这些事实表明,水溶性氮氧化物作为预防性抗氧化剂可干扰活性氧的生成,而膜内氮氧化物作为链断裂抗氧化剂可抑制脂质烷基自由基的形成。在脂质过氧化抑制反应过程中,膜内氮氧化物自由基引起的电子自旋共振(ESR)信号强度保持恒定,这表明脂质过氧化的预防与微粒体中氮氧化物与还原型氮氧化物之间的可逆氧化还原反应相关。通过还原膜内氮氧化物制备的还原型氮氧化物也可抑制TBA反应性物质的生成以及母体氮氧化物的生成。这些事实表明,膜内氮氧化物自由基或其还原形式“羟胺”可能是有用的亲脂性抗氧化剂。