Kagan V E, Prilipko L L, Savov V M, Pisarev V A, Eluashvili I A, Kozlov Iu P
Biokhimiia. 1979 Mar;44(3):482-9.
The participation of oxygen activated species in the induction of lipid peroxidation (LPO) in the membrane systems containing cytochrome P-450 (liver microsomes) and in the membrane fragments devoid of this hemoprotein (brain and skeletal muscle microsomes) was studied. It was shown that the rate of NADH-dependent LPO does not depend on the presence of hemoproteins and the activity of NADH-specific flavoprotein in the membranes. On the other hand, the microsomal membranes of the liver with high specific contents of b5 and P-450 cytochromes and NADPH-specific flavoprotein, had the highest rates of NADPH-dependent LPO. It was found that the most effective inhibitors of free oxygen activated species in the case of NADPH- and NADH-dependent LPO in the microsomal fractions of liver, brain and skeletal muscles are the superoxide (O ./2) anion radical inhibitors. The singlet oxygen (1O2) quenchers inhibit only NADPH-dependent LPO in the liver, however, in a far lesser degree. The hydroxyl radical (OH) scavengers had no effect on enzymatic LPO in all systems studied.
研究了氧活性物质在含细胞色素P - 450的膜系统(肝微粒体)和不含这种血红蛋白的膜片段(脑和骨骼肌微粒体)中诱导脂质过氧化(LPO)的参与情况。结果表明,NADH依赖性LPO的速率不取决于血红蛋白的存在以及膜中NADH特异性黄素蛋白的活性。另一方面,具有高含量b5和P - 450细胞色素以及NADPH特异性黄素蛋白的肝微粒体膜,其NADPH依赖性LPO的速率最高。结果发现,对于肝、脑和骨骼肌微粒体部分中NADPH和NADH依赖性LPO而言,最有效的游离氧活性物质抑制剂是超氧阴离子自由基(O₂⁻)抑制剂。单线态氧(¹O₂)猝灭剂仅在肝中抑制NADPH依赖性LPO,然而程度要小得多。羟基自由基(OH)清除剂对所有研究系统中的酶促LPO均无影响。