Littarru G P, Lippa S, De Sole P, Oradei A, Dalla Torre F, Macrì M
Biochem Biophys Res Commun. 1984 Mar 30;119(3):1056-61. doi: 10.1016/0006-291x(84)90881-7.
The ability of D-alpha-tocopherol to act as a quencher of (1)0(2) (singlet oxygen) was tested with a biological source of (1)0(2), namely the phagocytosis activated myeloperoxidase contained in the homogenate of human circulating polymorphonuclear leukocytes. With this system, the (1)0(2) quenching efficiency of exogenously added D-alpha-tocopherol was estimated from its inhibitory effect on the luminol amplified chemiluminescence. This inhibitory effect was dose dependent. D-alpha-tocopherol was also efficient in quenching the chemiluminescence generated through the H2O2-horseradish system. In both systems the quenching effect may be almost entirely "physical", since very little tocopherol was destroyed when compared to the relatively large amount of H2O2 consumed.
用一种生物源单线态氧(¹O₂),即人循环多形核白细胞匀浆中吞噬作用激活的髓过氧化物酶,测试了D-α-生育酚作为¹O₂猝灭剂的能力。在这个系统中,根据外源性添加的D-α-生育酚对鲁米诺增强化学发光的抑制作用,估算其¹O₂猝灭效率。这种抑制作用呈剂量依赖性。D-α-生育酚在猝灭通过H₂O₂-辣根过氧化物酶系统产生的化学发光方面也很有效。在这两个系统中,猝灭作用几乎完全可能是“物理性的”,因为与消耗的相对大量的H₂O₂相比,只有极少的生育酚被破坏。