Cervato G, Viani P, Cestaro B
Dept. of Medical Chemistry and Biochemistry, Faculty of Medicine, University of Milan, Italy.
Chem Phys Lipids. 1990 Dec;56(2-3):91-9. doi: 10.1016/0009-3084(90)90092-6.
Phosphate-containing compounds of both a lipophilic (dipalmitoylphosphatidic acid, lysophosphatidic acid and dicetylphosphate) and hydrophilic nature (orthophosphate, 3-phosphoglyceric acid, 2,3-diphosphoglyceric acid and pyrophosphate in particular) have been found to inhibit to varying degrees the lipoperoxidation of liposomal arachidonic acid. Lipophilic compounds seem to act exclusively at the lipid component level of the membrane, giving rise to polyanionic complexes with free arachidonic acid or its radical derivatives that could bind the Fe2+ strongly (thereby inhibiting the iron pro-oxidation activity) or to minimize the lateral mobility of the lipid radicals (thereby reducing the propagation of lipid peroxidation). The high antiperoxidative power of hydrophilic compounds, and in particular of pyrophosphate, must, on the contrary, be primarily attributed to their ability to form very stable complexes with the Fe present in the solution surrounding the liposomal membranes. The possible contribution of these physiological compounds to the in vivo defense mechanism against radical-induced damage is discussed.
已发现具有亲脂性(二棕榈酰磷脂酸、溶血磷脂酸和十六烷基磷酸酯)和亲水性(特别是正磷酸盐、3-磷酸甘油酸、2,3-二磷酸甘油酸和焦磷酸盐)的含磷化合物在不同程度上抑制脂质体花生四烯酸的脂质过氧化。亲脂性化合物似乎仅作用于膜的脂质成分水平,与游离花生四烯酸或其自由基衍生物形成聚阴离子复合物,这些复合物可以强烈结合Fe2+(从而抑制铁的促氧化活性)或使脂质自由基的侧向流动性最小化(从而减少脂质过氧化的传播)。相反,亲水性化合物,特别是焦磷酸盐的高抗过氧化能力,主要必须归因于它们与脂质体膜周围溶液中存在的铁形成非常稳定复合物的能力。讨论了这些生理化合物对体内抗自由基诱导损伤防御机制的可能贡献。