Rosen G M, Kloss M W, Rauckman E J
Mol Pharmacol. 1982 Nov;22(3):529-31.
Norcocaine nitroxide and N-hydroxynorcocaine were found to stimulate hepatic microsomal lipid peroxidation in vitro, as measured by spin-trapping techniques using the spin trap alpha-[4-pyridyl-1-oxide]-N-tert-butylnitrone. It was determined that either norcocaine nitroxide or N-hydroxynorcocaine markedly enhanced the rate of spin trapping of lipid peroxyl radicals when added to hepatic microsomal preparations. Glutathione, in the presence of dialyzed cytosol, inhibited the formation of lipid peroxyl spin-trapped adducts. This finding suggests that cytosolic glutathione-dependent enzymes perhaps including glutathione peroxidase play an important role in the prevention of norcocaine nitroxide-or N-hydroxynorcocaine-mediated lipid peroxidation.
通过使用自旋捕获剂α-[4-吡啶基-1-氧化物]-N-叔丁基硝酮的自旋捕获技术测定,发现去甲可卡因氮氧化物和N-羟基去甲可卡因在体外可刺激肝微粒体脂质过氧化。已确定,将去甲可卡因氮氧化物或N-羟基去甲可卡因添加到肝微粒体制剂中时,它们会显著提高脂质过氧自由基的自旋捕获速率。在透析后的胞质溶胶存在的情况下,谷胱甘肽可抑制脂质过氧自旋捕获加合物的形成。这一发现表明,胞质中依赖谷胱甘肽的酶(可能包括谷胱甘肽过氧化物酶)在预防去甲可卡因氮氧化物或N-羟基去甲可卡因介导的脂质过氧化中起重要作用。