Antunes F, Salvador A, Marinho H S, Alves R, Pinto R E
Grupo de Bioquímica e Biologia Teóricas, Instituto de Investigação Científica, Bento da Rocha Cabral, Lisboa, Portugal.
Free Radic Biol Med. 1996;21(7):917-43. doi: 10.1016/s0891-5849(96)00185-2.
An integrative mathematical model was developed to obtain an overall picture of lipid hydroperoxide metabolism in the mitochondrial inner membrane and surrounding matrix environment. The model explicitly considers an aqueous and a membrane phase, integrates a wide set of experimental data, and unsupported assumptions were minimized. The following biochemical processes were considered: the classic reactional scheme of lipid peroxidation; antioxidant and pro-oxidant effects of vitamin E; pro-oxidant effects of iron; action of phospholipase A2, glutathione-dependent peroxidases, glutathione reductase and superoxide dismutase; production of superoxide radicals by the mitochondrial respiratory chain; oxidative damage to proteins and DNA. Steady-state fluxes and concentrations as well as half-lives and mean displacements for the main metabolites were calculated. A picture of lipid hydroperoxide physiological metabolism in mitochondria in vivo showing the main pathways is presented. The main results are: (a) perhydroxyl radical is the main initiation agent of lipid peroxidation (with a flux of 10(-7)MS-1); (b) vitamin E efficiently inhibits lipid peroxidation keeping the amplification (kinetic chain length) of lipid peroxidation at low values (approximately equal to 10); (c) only a very minor fraction of lipid hydroperoxides escapes reduction via glutathione-dependent peroxidases; (d) oxidized glutathione is produced mainly from the reduction of hydrogen peroxide and not from the reduction of lipid hydroperoxides.
开发了一种综合数学模型,以全面了解线粒体内膜和周围基质环境中脂质过氧化氢的代谢情况。该模型明确考虑了水相和膜相,整合了大量实验数据,并将无根据的假设减至最少。考虑了以下生化过程:脂质过氧化的经典反应方案;维生素E的抗氧化和促氧化作用;铁的促氧化作用;磷脂酶A2、谷胱甘肽依赖性过氧化物酶、谷胱甘肽还原酶和超氧化物歧化酶的作用;线粒体呼吸链产生超氧自由基;蛋白质和DNA的氧化损伤。计算了主要代谢物的稳态通量和浓度以及半衰期和平均位移。展示了体内线粒体中脂质过氧化氢生理代谢的主要途径。主要结果如下:(a)过羟基自由基是脂质过氧化的主要引发剂(通量为10^(-7)MS^(-1));(b)维生素E有效地抑制脂质过氧化,使脂质过氧化的放大倍数(动力学链长)保持在较低值(约等于10);(c)只有极小部分的脂质过氧化氢通过谷胱甘肽依赖性过氧化物酶逃脱还原;(d)氧化型谷胱甘肽主要由过氧化氢的还原产生,而非脂质过氧化氢的还原产生。