PHOTOPROTECTION AND 5-MOP PHOTOCHEMOPROTECTION FROM UVR-INDUCED DNA DAMAGE IN HUMANS - THE ROLE OF SKIN TYPE

被引:62
作者
YOUNG, AR
POTTEN, CS
CHADWICK, CA
MURPHY, GM
HAWK, JLM
COHEN, AJ
机构
[1] CHRISTIE HOSP & HOLT RADIUM INST, PATERSON INST CANC RES, CANC RES CAMPAIGN DEPT EPITHELIAL BIOL, MANCHESTER M20 9BX, LANCS, ENGLAND
[2] TOXICOL ADVISORY SERV, SUTTON, SURREY, ENGLAND
关键词
D O I
10.1111/1523-1747.ep12491807
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Sites on previously unexposed buttock skin in 18 subjects (skin types I-V) were treated daily for 2 weeks with suberythemogenic doses of solar-simulated radiation (SSR) alone, SSR plus a UVB sunscreen, and SSR plus the same sunscreen with 5-methoxypsoralen at 30 ppm. The three sites of treatment (designated SSR, SSR/S, and SSR/S/5-MOP), and a control site that received no SSR or topical treatment, were challenged with 2MED SSR 1 week after the treatment had ceased. Biopsy samples, taken within 15 min after the challenge dose, were assessed for unscheduled DNA synthesis (UDS, interpreted as a measure of DNA damage), melanin deposition, and stratum corneum thickening. Within a given skin type, when compared with controls, the significant increase in either pigmentation or stratum corneum thickening was similar for SSR and SSR/S/5-MOP. SSR/S inhibited these endpoints. Compared with controls, UDS was significantly reduced in skin types III-V by SSR and in all skin types by SSR/S/5-MOP. SSR/S elicited no effect apart from minimal reductions in skin types IV and V. Thus, the increases in pigmentation and stratum corneum thickening seen in all skin types with SSR and SSR/S/5-MOP were accompanied by reduced UDS in all skin types with SSR/S/5-MOP but only in skin types III-V with SSR. These findings suggest that, although induced pigmentation and stratum corneum thickening may account in part for the reduction of UDS, qualitative differences in induced pigmentation may exist in skin types I-II between SSR and SSR/S/5-MOP treatments. The findings can also be interpreted to indicate that SSR/S/5-MOP treatment can afford protection against DNA damage from subsequent exposure to solar ultraviolet radiation. Risk-benefit considerations on the use of sunscreens with and without 5-MOP are discussed and the conclusion is drawn that the judicious use of 5-MOP sunscreens, particularly in skin types I-II, affords an alternative option to those seeking a suntan.
引用
收藏
页码:942 / 948
页数:7
相关论文
共 55 条
[1]   CHROMOSOME-DAMAGE INDUCED IN HUMAN-LYMPHOCYTES BY 5-METHOXYPSORALEN AND 8-METHOXYPSORALEN PLUS UV-A [J].
ABEL, G .
MUTATION RESEARCH, 1987, 190 (01) :63-68
[2]  
[Anonymous], 1987, J ROY COLL PHYS LOND, V21, P91
[3]   5-METHOXYPSORALEN, AN INGREDIENT IN SEVERAL SUNTAN PREPARATIONS, HAS LETHAL, MUTAGENIC AND CLASTOGENIC PROPERTIES [J].
ASHWOODSMITH, MJ ;
POULTON, GA ;
BARKER, M ;
MILDENBERGER, M .
NATURE, 1980, 285 (5764) :407-409
[4]   GENOTOXICITY OF BERGAPTEN AND BERGAMOT OIL IN SACCHAROMYCES-CEREVISIAE [J].
AVERBECK, D ;
AVERBECK, S ;
DUBERTRET, L ;
YOUNG, AR ;
MORLIERE, P .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY B-BIOLOGY, 1990, 7 (2-4) :209-229
[5]   THE VALUE OF TOPICAL SUNSCREENS CONTAINING PSORALENS [J].
BRENNER, W ;
GSCHNAIT, F .
ARCHIVES OF DERMATOLOGICAL RESEARCH, 1980, 267 (02) :189-190
[6]   TYROSINASE SYNTHESIS IN DIFFERENT SKIN TYPES AND THE EFFECTS OF ALPHA-MELANOCYTE-STIMULATING HORMONE AND CYCLIC-AMP [J].
BURCHILL, SA ;
MARKS, JM ;
THODY, AJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1990, 95 (05) :558-561
[7]  
CLEAVER JE, 1987, PHOTOMEDICINE, V2, P31
[8]   DEPLETION OF CUTANEOUS GLUTATHIONE BY ULTRAVIOLET-RADIATION [J].
CONNOR, MJ ;
WHEELER, LA .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (02) :239-245
[9]   NATURAL AND ARTIFICIAL PHOTOPROTECTION [J].
CRIPPS, DJ .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1981, 77 (01) :154-157
[10]   EARLY EFFECTS OF ULTRAVIOLET LIGHT ON DNA SYNTHESIS IN HUMAN SKIN IN VIVO [J].
EPSTEIN, WL ;
FUKUYAMA, K ;
EPSTEIN, JH .
ARCHIVES OF DERMATOLOGY, 1969, 100 (01) :84-+