Oettl K, Dikalov S, Freisleben H J, Mlekusch W, Reibnegger G
Medical Chemical Institute and Pregl Laboratory, Karl-Franzens-University Graz, Austria.
Biochem Biophys Res Commun. 1997 May 29;234(3):774-8. doi: 10.1006/bbrc.1997.6712.
Previously, it has been shown that pteridine derivatives are capable of modulating the action of free radicals and both prooxidant and antioxidant properties have been described. However, the mechanism of manifestation of these properties is still unclear. We studied the radical scavenging properties of 7,8-dihydroneopterin and neopterin using the spin trap 5,5-dimethyl-1-pyrroline-1-oxide (DMPO). It was found that dihydroneopterin acts generally as a radical scavenger. In the presence of dihydroneopterin the ESR signal was reduced by 30 to 90% compared to the control signal. The rate constants for the reactions of 7,8-dihydroneopterin with superoxide (10(3) M(-1) s(-1)) and peroxyl radicals (10(7) M(-1) s(-1)) were determined. Neopterin in contrast showed no reduction of the ESR signal except with superoxide radicals produced by xanthine oxidase. However, this effect was shown to be due to an inhibition of enzyme rather than to radical scavenging. Our results provide a basis for understanding previous observations of radical scavenger activity of 7,8-dihydroneopterin.
此前已表明,蝶啶衍生物能够调节自由基的作用,并且已描述了其促氧化和抗氧化特性。然而,这些特性表现的机制仍不清楚。我们使用自旋捕获剂5,5-二甲基-1-吡咯啉-1-氧化物(DMPO)研究了7,8-二氢新蝶呤和新蝶呤的自由基清除特性。发现二氢新蝶呤通常作为自由基清除剂起作用。与对照信号相比,在二氢新蝶呤存在下,电子自旋共振(ESR)信号降低了30%至90%。测定了7,8-二氢新蝶呤与超氧阴离子(10³ M⁻¹ s⁻¹)和过氧自由基(10⁷ M⁻¹ s⁻¹)反应的速率常数。相比之下,新蝶呤除了对黄嘌呤氧化酶产生的超氧阴离子自由基外,未显示出ESR信号的降低。然而,这种效应被证明是由于酶的抑制而不是自由基清除。我们的结果为理解先前关于7,8-二氢新蝶呤自由基清除活性的观察结果提供了基础。