Metabolic aspects of membrane lipid peroxidation.

J Wilhelm
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Abstract

Lipid peroxidation is a free radical initiated chain oxidation of unsaturated lipids. With respect to the ubiquity of unsaturated fatty acids in the cellular membranes, the peroxidative damage has the potential to affect many cellular functions. Some of the products of lipid peroxidation are diffusible and can spread the damage far beyond the site of the original free radical attack. There is an interdependency between reactive oxygen species and lipid peroxidation - reactive oxygen species initiate the reactions of lipid peroxidation and are also produced in these reactions as intermediates. The generation of reactive oxygen species can be triggered either by nonenzymatic mechanisms, in which iron ions play the major role, or by a wide range of enzymatic systems. The primary damaging effect of lipid peroxidation is exerted by the interactions with proteins and DNA. These interactions are then revealed at the subcellular (cellular organelles), cellular, and organ levels. The production of lipid peroxides interferes with the regulation of several metabolic pathways. In this review, particular attention is focused on the interaction of non-specifically formed lipid peroxides with the regulatory factors produced by the controlled oxidation of arachidonic acid (prostaglandins and leukotrienes), the effects on ionic pumps and intracellular calcium metabolism, the participation of lipid peroxidation in the ageing process, and the modulation of hormonal regulations by lipid peroxidation. Lipid peroxidation is induced at the level of the whole organism by various extrinsic factors such as ionizing irradiation, physical activity, diet and fasting, and various drugs. There is increasing awareness of the association between pathologic states and lipid peroxidation. Among the most studied are inflammation, ischaemia-reperfusion injury, and atherogenesis. Lipid peroxidation also plays a dual and complex role in cancer. Organisms have developed an efficient multilevel protective system against lipid peroxidation, but this can be overwhelmed by certain pathologies.

代谢方面的膜脂过氧化。
脂质过氧化是自由基引发的不饱和脂质的链式氧化。由于细胞膜中不饱和脂肪酸的普遍存在,其过氧化损伤有可能影响许多细胞功能。脂质过氧化的一些产物是可扩散的,可以将损伤扩散到远远超出原始自由基攻击的部位。活性氧与脂质过氧化反应之间存在相互依赖关系——活性氧引发脂质过氧化反应,并在这些反应中作为中间体产生。活性氧的产生既可以由非酶机制触发,其中铁离子起主要作用,也可以由广泛的酶系统触发。脂质过氧化的主要破坏作用是通过与蛋白质和DNA的相互作用发挥的。然后在亚细胞(细胞器)、细胞和器官水平上揭示这些相互作用。脂质过氧化物的产生干扰了几种代谢途径的调节。在这篇综述中,特别关注非特异性形成的脂质过氧化物与花生四烯酸(前列腺素和白三烯)氧化控制产生的调节因子的相互作用,对离子泵和细胞内钙代谢的影响,脂质过氧化在衰老过程中的参与,以及脂质过氧化对激素调节的调节。在整个机体水平上脂质过氧化是由多种外在因素引起的,如电离照射、身体活动、饮食和禁食以及各种药物。越来越多的人意识到病理状态和脂质过氧化之间的联系。其中研究最多的是炎症、缺血再灌注损伤和动脉粥样硬化。脂质过氧化在癌症中也起着双重和复杂的作用。生物体已经发展出一种有效的多级保护系统来对抗脂质过氧化,但这可能被某些病理所淹没。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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