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首页> 外文期刊>The Biochemical Journal >The mechanism of Fe2+-initiated lipid peroxidation in liposomes: the dual function of ferrous ions, the roles of the pre-existing lipid peroxides and the lipid peroxyl radical
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The mechanism of Fe2+-initiated lipid peroxidation in liposomes: the dual function of ferrous ions, the roles of the pre-existing lipid peroxides and the lipid peroxyl radical

机译:Fe2 +引发脂质体脂质过氧化的机制:亚铁离子的双重功能,预先存在的脂质过氧化物和脂质过氧化自由基的作用

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The mechanism of Fe2+-initiated lipid peroxidation in a liposomal system was studied. It was found that a second addition of ferrous ions within the latent period lengthened the time lag before lipid peroxidation started. The apparent time lag depended on the total dose of Fe2+ whenever the second dose of Fe2+ was added, which indicates that Fe2+ has a dual function: to initiate lipid peroxidation on one hand and suppress the species responsible for the initiation of the peroxidation on the other. When the pre-existing lipid peroxides (LOOH) were removed by incorporating triphenylphosphine into liposomes, Fe2+ could no longer initiate lipid peroxidation and the acceleration of Fe2+ oxidation by the liposomes disappeared. However, when extra LOOH were introduced into liposomes, both enhancement of the lipid peroxidation and shortening of the latent period were observed. When the scavenger of lipid peroxyl radicals (LOO.), N,N'-diphenyl-p-phenylene-diamine, was incorporated into liposomes, neither initiation of the lipid peroxidation nor acceleration of the Fe2+ oxidation could be detected. The results may suggest that both the pre-existing LOOH and LOO. are necessary for the initiation of lipid peroxidation. The latter comes initially from the decomposition of the pre-existing LOOH by Fe2+ and can be scavenged by its reaction with Fe2+. Only when Fe2+ is oxidized to such a degree that LOO. is no longer effectively suppressed does lipid peroxidation start. It seems that by taking the reactions of Fe2+ with LOOH and LOO. into account, the basic chemistry in lipid peroxidation can explain fairly well the controversial phenomena observed in Fe2+-initiated lipid peroxidation, such as the existence of a latent period, the critical ratio of Fe2+ to lipid and the required oxidation of Fe2+. [References: 33]
机译:研究了脂质体系统中Fe2 +引发脂质过氧化的机理。发现在潜伏期内第二次添加亚铁离子延长了脂质过氧化开始之前的时间延迟。每当添加第二剂Fe2 +时,表观时间差取决于Fe2 +的总剂量,这表明Fe2 +具有双重功能:一方面引发脂质过氧化,另一方面抑制引起过氧化的物种。当通过将三苯基膦掺入脂质体中来清除先前存在的脂质过氧化物(LOOH)时,Fe2 +不再能够引发脂质过氧化作用,并且脂质体对Fe2 +氧化的加速作用也消失了。然而,当将额外的LOOH引入脂质体中时,观察到脂质过氧化作用的增强和潜伏期的缩短。当脂质过氧化物自由基(LOO。)的清除剂,N,N'-二苯基-对亚苯基-二胺被掺入脂质体中时,既没有检测到脂质过氧化的开始,也没有检测到Fe2 +氧化的加速。结果可能表明既存在的LOOH和LOO。是引发脂质过氧化反应所必需的。后者最初来自Fe 2+对先前存在的LOOH的分解,并且可以通过其与Fe 2+的反应进行清除。仅当Fe2 +被氧化至LOO的程度时。不再有效地抑制脂质过氧化作用的开始。似乎是通过采用Fe2 +与LOOH和LOO的反应。考虑到这一点,脂质过氧化反应的基本化学原理可以很好地解释在Fe2 +引发的脂质过氧化反应中观察到的有争议的现象,例如潜伏期的存在,Fe2 +与脂质的临界比以及所需的Fe2 +氧化。 [参考:33]

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