Sliwinski Tomasz, Rozej Wioletta, Morawiec-Bajda Alina, Morawiec Zbigniew, Reiter Russel, Blasiak Janusz
Department of Molecular Genetics, University of Lodz, Banacha 12/16, 90-237, Lodz, Poland.
Mutat Res. 2007 Dec 1;634(1-2):220-7. doi: 10.1016/j.mrgentox.2007.07.013. Epub 2007 Aug 9.
Melatonin is a hormone-like substance that has a variety of beneficial properties as regulator of the circadian rhythm and as anti-inflammatory and anti-cancer agent. The latter activity can be linked with the ability of melatonin to protect DNA against oxidative damage. It may exert such action either by scavenging reactive oxygen species or their primary sources, or by stimulating the repair of oxidative damage in DNA. Since such type of DNA damage is reflected in oxidative base modifications that are primarily repaired by base-excision repair (BER), we tried to investigate in the present work whether melatonin could influence this DNA-repair system. We also investigated the ability of melatonin to inactivate hydrogen peroxide, a potent source of reactive oxygen species. Melatonin at 50 microM and its direct metabolite N(1)-acetyl-N(2)-formyl-5-methoxykynuramine reduced DNA damage induced by hydrogen peroxide at approximately the same ratio. Melatonin stimulated the repair of DNA damage induced by hydrogen peroxide, as assessed by the alkaline comet assay. However, melatonin at 50 microM had no impact on the activity in vitro of three glycosylases playing a pivotal role in BER: Endo III, Fpg and ANPG 80. On the other hand, melatonin chemically inactivated hydrogen peroxide, reducing its potential to damage DNA. And finally, melatonin did not influence the repair of an a-basic (AP) site by cellular extracts, as was evaluated by a functional BER assay in vitro. In conclusion, melatonin can have a protective effect against oxidative DNA damage by chemical inactivation of a DNA-damaging agent as well as by stimulating DNA repair, but key factors in BER, viz. glycosylases and AP-endonucleases, do not seem to be affected by melatonin. Further study with other components of the BER machinery and studies aimed at other DNA-repair systems are needed to clarify the mechanism underlying the stimulation of DNA repair by melatonin.
褪黑素是一种类似激素的物质,作为昼夜节律的调节剂以及抗炎和抗癌剂,具有多种有益特性。后者的活性可能与褪黑素保护DNA免受氧化损伤的能力有关。它可能通过清除活性氧物种或其主要来源,或通过刺激DNA氧化损伤的修复来发挥这种作用。由于这种类型的DNA损伤反映在主要通过碱基切除修复(BER)修复的氧化碱基修饰中,我们在本研究中试图探究褪黑素是否会影响这种DNA修复系统。我们还研究了褪黑素灭活过氧化氢(一种活性氧物种的强大来源)的能力。50微摩尔的褪黑素及其直接代谢产物N(1)-乙酰-N(2)-甲酰基-5-甲氧基犬尿胺以大致相同的比例减少了过氧化氢诱导的DNA损伤。通过碱性彗星试验评估,褪黑素刺激了过氧化氢诱导的DNA损伤的修复。然而,50微摩尔的褪黑素对在BER中起关键作用的三种糖苷酶的体外活性没有影响:内切酶III、Fpg和ANPG 80。另一方面,褪黑素通过化学方法使过氧化氢失活,降低了其损伤DNA的潜力。最后,通过体外功能性BER试验评估,褪黑素不影响细胞提取物对无碱基(AP)位点的修复。总之,褪黑素可以通过化学灭活DNA损伤剂以及刺激DNA修复来对氧化DNA损伤起到保护作用,但BER中的关键因素,即糖苷酶和AP内切酶,似乎不受褪黑素影响。需要对BER机制的其他成分进行进一步研究以及针对其他DNA修复系统的研究,以阐明褪黑素刺激DNA修复的潜在机制。