Tesoriere L, D'Arpa D, Re R, Livrea M A
Istituto di Farmacologia e Farmacognosia, Universita' di Palermo, Italy.
Arch Biochem Biophys. 1997 Jul 1;343(1):13-8. doi: 10.1006/abbi.1997.0128.
Lipoperoxyl radical-scavenging activity of retinol in unilamellar soybean phosphatidylcholine liposomes was studied under a variety of conditions to appreciate to what extend retinol may be considered an effective antioxidant. Peroxidation, initiated by 2 mM 2,2'-azobis(amidino-propane)hydrochloride (AAPH), was carried out at 160 torr O2 or at 15 torr O2, in the absence or in the presence of 10 to 40 mM retinol. As evaluated by the length of the inhibition periods, t(inh), and by the ratio between the inhibition and propagation rate, R(inh)/R(p), the antioxidant activity of retinol was higher at 15 torr O2 than at 160 torr O2. The consumption rate of retinol was markedly faster at 160 torr O2 than at 15 torr O2 and increased with the increase of retinol concentration under both oxygen tensions. When liposome peroxidation was carried out under N2, retinol consumption was independent of retinol concentration. Peroxyl radicals oxidize retinol to 5,6-retinol epoxide. The ratio between 5,6-epoxide formed and the retinol consumed was markedly higher at 15 torr O2 than under air and decreased with the increased retinol concentrations. When butylated hydroxytoluene was included into the liposomal suspension, most of the consumed retinol was converted into 5,6-epoxide. Liposomes were incubated at 15 torr O2, in the presence of 0.5 to 10 mM AAPH. The antioxidant effectiveness of 40 mM retinol, as measured by the R(inh)/R(p) ratio, increased with the increase of the radical fluxes. The results suggest, besides radical trapping, that a major consumption of retinol during lipid oxidation occurs through self-oxidation reactions, which are concentration- and oxygen-dependent. A decreased self-oxidation makes retinol a better lipoperoxyl radical scavenger at low, rather than at high partial pressure of oxygen. However, when self-oxidation of retinol is prevented, only a minor fraction of the antioxidant is allowed to effectively act as a radical scavenger, suggesting that the radical-trapping reactions are rate-limiting for the antioxidant process. Peroxyl radical concentration, by shifting the route of the retinol activity toward radical scavenging, brings about an increasingly more efficient radical trapping. It is concluded that all-trans retinol behaves as a more effective antioxidant at low oxygen partial pressure, low retinol concentrations, and high radical flux.
在各种条件下研究了视黄醇在单层大豆磷脂酰胆碱脂质体中的脂过氧自由基清除活性,以了解视黄醇在多大程度上可被视为一种有效的抗氧化剂。由2 mM 2,2'-偶氮二(脒基丙烷)盐酸盐(AAPH)引发的过氧化反应,在160托氧气或15托氧气条件下进行,反应体系中不存在或存在10至40 mM视黄醇。通过抑制期的时长t(inh)以及抑制速率与传播速率之比R(inh)/R(p)评估,视黄醇在15托氧气条件下的抗氧化活性高于在160托氧气条件下。视黄醇的消耗速率在160托氧气条件下明显快于在15托氧气条件下,并且在两种氧分压下均随视黄醇浓度的增加而增加。当脂质体过氧化反应在氮气氛围下进行时,视黄醇的消耗与视黄醇浓度无关。过氧自由基将视黄醇氧化为5,6-视黄醇环氧化物。在15托氧气条件下形成的5,6-环氧化物与消耗的视黄醇之比明显高于在空气中的情况,并且随视黄醇浓度的增加而降低。当将丁基化羟基甲苯加入脂质体悬浮液中时,大部分消耗的视黄醇转化为5,6-环氧化物。脂质体在15托氧气条件下,存在0.5至10 mM AAPH的情况下进行孵育。通过R(inh)/R(p)比值测量,40 mM视黄醇的抗氧化效果随自由基通量的增加而增强。结果表明,除了自由基捕获外,脂质氧化过程中视黄醇的主要消耗是通过自氧化反应发生的,这些自氧化反应与浓度和氧气有关。自氧化反应的减少使视黄醇在低氧分压而非高氧分压下成为更好的脂过氧自由基清除剂。然而,当视黄醇的自氧化被阻止时,只有一小部分抗氧化剂能够有效地作为自由基清除剂起作用,这表明自由基捕获反应是抗氧化过程的限速步骤。过氧自由基浓度通过将视黄醇活性的途径转向自由基清除,导致自由基捕获越来越有效。得出的结论是,全反式视黄醇在低氧分压、低视黄醇浓度和高自由基通量下表现为更有效的抗氧化剂。