Arkhipenko Iu V, Dobrina S K, Kagan V E, Kozlov Iu P, Nadirov N K, Pisarev V A, Ritov V B, Khafizov R Kh
Biokhimiia. 1977 Aug;42(8):1525-31.
Mechanisms of the inhibitory effect of vitamin E on the process of lipid peroxidation (LPO) in biological membranes are studied. Both alpha-tocopherol and its derivatives (a-tocopherylacetate, o- and p-tocopherylquinones possess no radical scavenging activity) inhibit non-enzymatic (Fe2+ + ascorbate)-induced LPO and prevent LPO-dependent inhibition of Ca2+ transport in sarcoplasmic reticulum membranes from skeletal muscles. The protective effect of alpha-tocopherylacetate, tocopherilquinones and partially of alpha-tocopherol is due to a stabilizing effect of these compounds on sarcoplasmic reticulum membranes, registered by a decrease of fluidity of membrane lipid bilayer (probed by nitroxile radical TEMPO) and by a decrease of its passive permeability for Ca2+. Under the enzymatic NADPH-dependent LPO induction in rat liver microsomal fraction a strong inhibitory effect of tocopherylquinones is similar to the effect of other electron acceptors (methylnaphtoquinone, TEMPO) and is due to their ability to compete with LPO reaction for reducing equivalents in NADPH-dependent electron carriers wich results in the formation of hydroxy-derivatives having pronounced radical scavenging activity.
研究了维生素E对生物膜中脂质过氧化(LPO)过程的抑制作用机制。α-生育酚及其衍生物(α-生育酚乙酸酯、邻-和对-生育醌均不具有自由基清除活性)可抑制非酶促(Fe2+ + 抗坏血酸)诱导的LPO,并防止LPO依赖性对骨骼肌肌浆网膜中Ca2+转运的抑制。α-生育酚乙酸酯、生育醌以及部分α-生育酚的保护作用归因于这些化合物对肌浆网膜的稳定作用,这可通过膜脂质双层流动性的降低(由硝酰自由基TEMPO探测)以及其对Ca2+的被动通透性的降低来证明。在大鼠肝微粒体部分依赖NADPH的酶促LPO诱导下,生育醌的强烈抑制作用类似于其他电子受体(甲基萘醌、TEMPO)的作用,这是由于它们能够与LPO反应竞争NADPH依赖性电子载体中的还原当量,从而导致形成具有明显自由基清除活性的羟基衍生物。