Total antioxidant capacity and nuclear DNA damage in keratinocytes after exposure to H2O2

被引:19
作者
Armeni, T
Battino, M
Stronati, A
Pugnaloni, A
Tomassini, G
Rosi, G
Biagini, G
Principato, G [1 ]
机构
[1] Univ Ancona, Inst Biol & Genet, I-60100 Ancona, Italy
[2] Univ Ancona, Inst Biochem, I-60100 Ancona, Italy
[3] Univ Ancona, Inst Human Morphol, I-60100 Ancona, Italy
[4] Univ Perugia, Inst Cellular Biol, I-06100 Perugia, Italy
[5] Univ Perugia, Sch Plast Surg, I-06100 Perugia, Italy
关键词
antioxidant enzymes; DNA damage; hydrogen peroxide; keratinocytes; total antioxidant capacity;
D O I
10.1515/BC.2001.205
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Studies of oxidative stress have classically been performed by analyzing specific, single antioxidants. In this study, susceptibility to oxidative stress in the human keratinocyte cell line NCTC2544 exposed to hydrogen peroxide (H2O2) was measured by the TOSC (total oxyradical scavenging capacity) assay, which discriminates between the antioxidant capacity toward peroxyl radicals and hydroxyl radical. The generation of H2O2-induced DNA damage, total antioxidant capacity and levels of antioxidant enzymes (catalase, superoxide dismutase, glutathione reductase, glutathione S-transferase, glutathione peroxidase) were studied. Exposure to H2O2-induced DNA damage that was gradually restored while a significant reduction in cellular TOSC values was obtained independently of stressor concentrations and the degree of DNA repair. Whereas TOSC values and cell resistance to H2O2 showed a good relationship, the extent of DNA damage is independent from cellular total antioxidant capacity. Indeed, maximum DNA damage and cell mortality were observed in the first 4 h, whereas TOSC remained persistently low until 48 h. Catalase levels were significantly lower in exposed cells after 24 and 48 h. Keratinocytes exposed after 48 h to a second H2O2 treatment exhibited massive cell death. A possible linkage was observed between TOSC values and NCTC2544 resistance to H2O2 challenge. The TOSC assay appears to be a useful tool for evaluating cellular resistance to oxidative stress.
引用
收藏
页码:1697 / 1705
页数:9
相关论文
共 35 条
  • [1] Oxidative stress and gene regulation
    Allen, RG
    Tresini, M
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (03) : 463 - 499
  • [2] ALLEN RG, 1993, FREE RADICALS AGING, P11
  • [3] Claiborne A., 1985, Handbook of Methods of Oxygen Radicals Research, DOI DOI 10.1016/0531-5565(85)90021-X
  • [4] Increased oxidative modification of albumin when illuminated in vitro in the presence of a common sunscreen ingredient: Protection by nitroxide radicals
    Damiani, E
    Carloni, P
    Biondi, C
    Greci, L
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2000, 28 (02) : 193 - 201
  • [5] FREE-RADICALS IN CUTANEOUS BIOLOGY
    DARR, D
    FRIDOVICH, I
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1994, 102 (05) : 671 - 675
  • [6] Biomarkers of free radical damage applications in experimental animals and in humans
    De Zwart, LL
    Meerman, JHN
    Commandeur, JNM
    Vermeulen, NPE
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1999, 26 (1-2) : 202 - 226
  • [7] The influence of cell growth, detoxifying enzymes and DNA repair on hydrogen peroxide-mediated DNA damage (measured using the comet assay) in human cells
    Duthie, SJ
    Collins, AR
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 1997, 22 (04) : 717 - 724
  • [8] Whale songs lengthen in response to sonar
    Miller, PJO
    Biassoni, N
    Samuels, A
    Tyack, PL
    [J]. NATURE, 2000, 405 (6789) : 903 - 903
  • [9] Free radicals and hearing - Cause, consequence, and criteria
    Evans, P
    Halliwell, B
    [J]. OTOTOXICITY: BASIC SCIENCE AND CLINICAL APPLICATIONS, 1999, 884 : 19 - 40
  • [10] Habig W H, 1981, Methods Enzymol, V77, P398