ULTRAVIOLET-A - INDUCED LIPID-PEROXIDATION AND ANTIOXIDANT DEFENSE SYSTEMS IN CULTURED HUMAN SKIN FIBROBLASTS

被引:103
作者
MOYSAN, A
MARQUIS, I
GABORIAU, F
SANTUS, R
DUBERTRET, L
MORLIERE, P
机构
[1] HOP HENRI MONDOR,DERMATOL LAB,INSERM,U312,RUE DE LATTRE TASSIGNY,F-94010 CRETEIL,FRANCE
[2] HOP ST LOUIS,SERV DERMATOL,INSERM,U312,F-75010 PARIS,FRANCE
[3] MUSEUM NATL HIST NAT,PHYS CHIM ADAPAT BIOL LAB,INSERM U312,F-75231 PARIS 05,FRANCE
关键词
D O I
10.1111/1523-1747.ep12472352
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Cultured human skin fibroblasts from healthy donors were irradiated with 180 kJ.m-2 ultraviolet (UV) A (320400 nm) and assayed for thiobarbituric acid-reactive substances (TBARS), taken as an indicator of lipid peroxidation. Antioxidant defenses, including total glutathione (GSH) levels, superoxide dismutase (SOD), glutathione peroxidase (GSHPx), and catalase (Cat) activities were simultaneously assayed before and after irradiation. For the various donors, with different activities of these antioxidant systems before irradiation, TBARS correlated positively with SOD activity and negatively with Cat activity, whereas no correlation with GSH level or GSHPx activity was found. These data support the view that O2- is generated by UVA irradiation. They also suggest that H2O2, arising from O2- dismutation by SOD is not completely removed by Cat. Thus, the sensitivity of human fibroblasts to UVA-induced lipid peroxidation depends on a balance between SOD and Cat activities. After UVA irradiation, Cat activity was strongly inhibited, whereas GSH level was slightly decreased. By contrast, GSHPx and SOD activity remained unchanged after UVA irradiation.
引用
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页码:692 / 698
页数:7
相关论文
共 68 条
[1]   THE BALANCE BETWEEN CU,ZN-SUPEROXIDE DISMUTASE AND CATALASE AFFECTS THE SENSITIVITY OF MOUSE EPIDERMAL-CELLS TO OXIDATIVE STRESS [J].
AMSTAD, P ;
PESKIN, A ;
SHAH, G ;
MIRAULT, ME ;
MORET, R ;
ZBINDEN, I ;
CERUTTI, P .
BIOCHEMISTRY, 1991, 30 (38) :9305-9313
[2]   CATALASE - KINETICS OF PHOTOOXIDATION [J].
ARONOFF, S .
SCIENCE, 1965, 150 (3692) :72-&
[3]  
AUST SD, 1986, HDB METHODS OXYGEN R, P203
[4]   MICROTITER PLATE ASSAY FOR THE MEASUREMENT OF GLUTATHIONE AND GLUTATHIONE DISULFIDE IN LARGE NUMBERS OF BIOLOGICAL SAMPLES [J].
BAKER, MA ;
CERNIGLIA, GJ ;
ZAMAN, A .
ANALYTICAL BIOCHEMISTRY, 1990, 190 (02) :360-365
[5]  
BEERS RF, 1952, J BIOL CHEM, V195, P133
[6]   POTENTIAL INVOLVEMENT OF FREE-RADICAL REACTIONS IN ULTRAVIOLET LIGHT-MEDIATED CUTANEOUS DAMAGE [J].
BLACK, HS .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (02) :213-221
[7]   DNA STRAND SCISSION BY ENZYMICALLY GENERATED OXYGEN RADICALS [J].
BRAWN, K ;
FRIDOVICH, I .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1981, 206 (02) :414-419
[8]  
BRODTHAGEN H, 1986, BIOL EFFECTS UVA RAD, P127
[9]   PHOTODAMAGE TO HEPATOCYTES BY VISIBLE-LIGHT [J].
CHENG, LYL ;
PACKER, L .
FEBS LETTERS, 1979, 97 (01) :124-128
[10]  
Clairborne A, 1986, HDB METHODS OXYGEN R, P283