McCray P B, Gibson D D, Fong K L, Hornbrook K R
Biochim Biophys Acta. 1976 Jun 22;431(3):459-68.
Results are presented indicating that, although glutathione peroxidase activity inhibits lipid peroxidation in membranes, it does not appear to do so by reducing membrane lipid peroxides to lipid alcohols, as has been shown by others to be the case for free fatty acid peroxides in solution. Lipid peroxidation was studied in an enzymic system (microsomal NADPH oxidase) and in a non-enzymic system (mitochondria plus ascorbate). A study of the fatty acids in the phospholipids of microsomes and mitochondria demonstrated that detectable amounts of hydroxy fatty acids were not formed in the membranes when the latter were incubated in the presence of the glutathione peroxidase system even under conditions known to have generated significant levels of lipid peroxides in the membrane. Fatty acid analyses of the microsomal and mitochondrial particles indicated that glutathione peroxidase activity inhibited loss of polyunsaturated fatty acids when these organelles were exposed to peroxidizing conditions. If glutathione peroxidase activity were inhibiting the formation of malondialdehyde (a product of lipid peroxidation) by converting peroxide groups to alcohols, the loss of the constitutive polyunsaturated fatty acids in the membrane should not have been appreciably affected by addition of the peroxidase system. The protective effect cannot be due to quenching of an autocatalytic type of lipid peroxidation (at least in the microsomal system) since it has been established that the microsomal enzyme system (NADPH oxidase) catalyzes a continuous attack on microsomal polyunsaturated fatty acyl groups during the reaction and that the peroxidative process is not autocatalytic in nature. It appears, therefore, that glutathione peroxidase activity must exert its effect on this system by preventing free radical attack on the polyunsaturated membrane lipids in the first place. A possible mechanism for the interruption of a free radical attack on the lipids is proposed.
研究结果表明,尽管谷胱甘肽过氧化物酶活性可抑制膜中的脂质过氧化作用,但它似乎并非像其他人所表明的溶液中游离脂肪酸过氧化物那样,通过将膜脂质过氧化物还原为脂质醇来实现这一作用。在酶系统(微粒体NADPH氧化酶)和非酶系统(线粒体加抗坏血酸)中研究了脂质过氧化作用。对微粒体和线粒体磷脂中的脂肪酸进行的一项研究表明,当微粒体和线粒体在谷胱甘肽过氧化物酶系统存在的情况下孵育时,即使在已知会在膜中产生大量脂质过氧化物的条件下,膜中也不会形成可检测量的羟基脂肪酸。对微粒体和线粒体颗粒的脂肪酸分析表明,当这些细胞器暴露于过氧化条件时,谷胱甘肽过氧化物酶活性可抑制多不饱和脂肪酸的损失。如果谷胱甘肽过氧化物酶活性通过将过氧化物基团转化为醇来抑制丙二醛(脂质过氧化产物)的形成,那么膜中组成性多不饱和脂肪酸的损失应该不会因添加过氧化物酶系统而受到明显影响。这种保护作用不可能是由于淬灭了一种自催化类型 的脂质过氧化作用(至少在微粒体系统中),因为已经确定微粒体酶系统(NADPH氧化酶)在反应过程中催化对微粒体多不饱和脂肪酰基的持续攻击,并且过氧化过程本质上不是自催化的。因此,似乎谷胱甘肽过氧化物酶活性必须首先通过防止自由基对多不饱和膜脂质的攻击来对该系统发挥作用。本文提出了一种自由基对脂质攻击的中断机制。