Effect of solution ionic strength on lipid peroxidation initiation by the perhydroxyl (xanthine oxidase-derived) and peroxyl radicals.
Effect of solution ionic strength on lipid peroxidation initiation by the perhydroxyl (xanthine oxidase-derived) and peroxyl radicals.
复制标题
溶液离子强度对过羟基(黄嘌呤氧化酶衍生的)和过氧自由基引发脂质过氧化的影响。
DOI:
10.1021/tx00026a018
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发表时间:
1992
影响因子:
4.1
通讯作者:
Dix,TA
中科院分区:
文献类型:
--
作者:
Aikens,J;Dix,TA
The role of solution ionic strength in perhydroxyl (HOO*) and peroxyl (ROO*) radical initiated lipid peroxidation has been defined and investigated. Xanthine oxidase activity was used as the source of superoxide (02 “) and its conjugate acid (HOO*) in these experiments. While the enzyme’s activity varied with changes in ionic strength, the effect could be factored out of the lipid peroxidation studies. Both HOO*-and ROO'-initiated peroxidations of linoleic acid were promoted by increases in solution ionic strength: the inclusion of 0.1 M of various alkali metal salts in the reaction resulted in up to a 4-fold increase in theoverall peroxidation rate. Significant differences between alkali metal cations (Li+, Na+, K+, Cs+) and halogen anions (F", Cl", Br") were not observed. Thus, the increased rates of lipid peroxidation were attributable to changes in solution ionic strength rather than specific ion-reaction interactions. Ionicstimulation of lipid peroxidation occurred only in the presence of preexisting fatty acid hydroperoxides (LOOHs), which provided additional support for the hydrogen atom transfer mechanism previously proposed [Aikens, J., and Dix, T. A.(1991) J. Biol. Chem. 266, 15091] for the HOO*/LOOH initiation process. Physiologically appropriate salt concentrations were used in these studies, hence the results may have biological significance.