Stratton S P, Liebler D C
Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona 85721, USA.
Biochemistry. 1997 Oct 21;36(42):12911-20. doi: 10.1021/bi9708646.
Photosensitized oxidation reactions damage tissue by catalyzing the formation of oxyradicals and singlet oxygen. beta-Carotene is hypothesized to exert photoprotective effects by quenching singlet oxygen formed by Type II reactions and by scavenging free radicals formed by Type I reactions. beta-Carotene antioxidant mechanisms were studied in a phospholipid membrane model of photooxidation with a new isotope dilution gas chromatography-mass spectrometry (GC-MS) assay that quantitatively distinguishes singlet oxygen-mediated and radical-mediated lipid peroxidation. This assay measures 9- and 10-hydroxylinoleate methyl esters and was used to generate photooxidation profiles for the photosensitizers methylene blue, Rose Bengal, and tetraphenylporphine. These profiles indicate a shift from Type II to Type I photooxidation mechanisms in later stages of photooxidation. beta-Carotene (0.45 mol %) inhibited singlet oxygen-mediated lipid peroxidation at early stages of methylene blue-sensitized photooxidation. Production of radical-mediated products increased faster than singlet oxygen-mediated products at later stages. beta-Carotene-5,8-endoperoxide, a specific marker for singlet oxygen oxidation of beta-carotene in solution, was unstable under the incubation conditions and was not detected in this system. alpha-Tocopherol (0.45 mol %) was ineffective in inhibiting photosensitized lipid peroxidation, whereas 4.5 mol % alpha-tocopherol inhibited almost all radical-mediated lipid peroxidation as well as early-stage singlet oxygen-mediated lipid peroxidation. Cumene hydroperoxide stimulated radical-mediated lipid peroxidation, indicating that accumulation of hydroperoxides from Type II photooxidation may enhance Type I reactions. These data suggest that singlet oxygen quenching, rather than radical scavenging reactions, accounts for the photoprotective actions of beta-carotene.
光敏氧化反应通过催化氧自由基和单线态氧的形成来损伤组织。据推测,β-胡萝卜素通过淬灭II型反应形成的单线态氧以及清除I型反应形成的自由基来发挥光保护作用。在光氧化的磷脂膜模型中,采用一种新的同位素稀释气相色谱-质谱联用(GC-MS)分析方法对β-胡萝卜素的抗氧化机制进行了研究,该方法能够定量区分单线态氧介导的和自由基介导的脂质过氧化反应。该分析方法可测定9-和10-羟基亚油酸甲酯,并用于生成亚甲蓝、孟加拉玫瑰红和四苯基卟啉等光敏剂的光氧化图谱。这些图谱表明在光氧化后期,光氧化机制从II型转变为I型。在亚甲蓝敏化的光氧化早期阶段,β-胡萝卜素(0.45摩尔%)抑制了单线态氧介导的脂质过氧化反应。在后期,自由基介导产物的生成速度比单线态氧介导产物增加得更快。β-胡萝卜素-5,8-内过氧化物是溶液中β-胡萝卜素单线态氧氧化的特异性标志物,在孵育条件下不稳定,在该系统中未检测到。α-生育酚(0.45摩尔%)在抑制光敏脂质过氧化方面无效,而4.5摩尔%的α-生育酚几乎抑制了所有自由基介导的脂质过氧化以及早期单线态氧介导的脂质过氧化。异丙苯过氧化氢刺激了自由基介导的脂质过氧化,表明II型光氧化产生的氢过氧化物积累可能会增强I型反应。这些数据表明,β-胡萝卜素的光保护作用是通过淬灭单线态氧,而非清除自由基反应来实现的。