Increased cyclooxygenase expression and thymine dimer formation after repeated exposures of humans to low doses of solar simulated radiation

被引:9
作者
Narbutt, Joanna
Lesiak, Aleksandra
Jochymski, Cezary
Kozlowski, Wojciech
Sysa-Jedrzejowska, Anna
Norval, Mary
机构
[1] Med Univ Lodz, Dept Dermatol, PL-94017 Lodz, Poland
[2] Mil Med Inst, Dept Pathol, Warsaw, Poland
[3] Univ Edinburgh, Sch Med, Edinburgh, Midlothian, Scotland
关键词
cyclooxygenase-1; and; 2; photoadaptation; photoprotection; solar simulated radiation; thymine dimers;
D O I
10.1111/j.1600-0625.2007.00598.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
The impact of repeated doses of solar simulated radiation (SSR) has not been evaluated, particularly to determine if photoadaptation and photoprotection develop over time. In this study, erythema, pigmentation, cyclooxygenase (COX)-1 and 2 expression and thymine dimer (dTT) formation were evaluated in the skin of irradiated subjects of phototype II or III. Groups of 7-10 volunteers were whole-body irradiated with a low dose of SSR on each of 10 consecutive days followed by a single erythemal ultraviolet B (UVB) dose on a small body area, or irradiated only with the single erythemal UVB dose on a small body area, or irradiated with the low dose of SSR on each of 30 consecutive days, or were unirradiated. Erythema and pigmentation were measured 24 h after the final SSR or UVB, and skin biopsies collected for the assessment of COX+ cells and dTT(+) nuclei. The repeated SSR exposures induced a small increase in pigmentation without erythema, and were slightly protective against the erythemal effects of the subsequent high UVB dose. The number of COX-1(+) and 2(+) cells increased as a result of 10-days SSR and rose still further after 30-days SSR, indicating that photoadaptation had not developed. The SSR exposures did not result in any protection against the further increase in COX-1 and 2 expression caused by the erythemal UVB dose. In contrast, for dTT formation, the repeated SSR exposures led to a limited degree of both photoadaptation and photoprotection.
引用
收藏
页码:837 / 843
页数:7
相关论文
共 38 条
[1]  
Al Mahroos M, 2002, ARCH DERMATOL, V138, P1480
[2]  
An KP, 2002, PHOTOCHEM PHOTOBIOL, V76, P73, DOI 10.1562/0031-8655(2002)076<0073:CEIMAH>2.0.CO
[3]  
2
[4]   Ultraviolet B (UVB)-induced COX-2 expression in murine skin: An immunohistochemical study [J].
Athar, M ;
An, KP ;
Morel, KD ;
Kim, AL ;
Aszterbaum, M ;
Longley, J ;
Epstein, EH ;
Bickers, DR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (04) :1042-1047
[5]   [Nle4-D-Phe7]-α-melanocyte-stimulating hormone significantly increased pigmentation and decreased UV damage in fair-skinned Caucasian volunteers [J].
Barnetson, Ross StC. ;
Ooi, Terry K. T. ;
Zhuang, Liqing ;
Halliday, Gary M. ;
Reid, Catherine M. ;
Walker, Patrick C. ;
Humphrey, Stuart M. ;
Kleinig, Michael J. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (08) :1869-1878
[6]  
BECHTHOMSEN N, 1994, PHOTODERMATOL PHOTO, V10, P53
[7]   UV EXPOSURE REDUCES IMMUNIZATION RATES AND PROMOTES TOLERANCE TO EPICUTANEOUS ANTIGENS IN HUMANS - RELATIONSHIP TO DOSE, CD1A-DR+ EPIDERMAL MACROPHAGE INDUCTION, AND LANGERHANS CELL DEPLETION [J].
COOPER, KD ;
OBERHELMAN, L ;
HAMILTON, TA ;
BAADSGAARD, O ;
TERHUNE, M ;
LEVEE, G ;
ANDERSON, T ;
KOREN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (18) :8497-8501
[8]   Sources and measurement of ultraviolet radiation [J].
Diffey, BL .
METHODS, 2002, 28 (01) :4-13
[9]   DNA damage enhances melanogenesis [J].
Eller, MS ;
Ostrom, K ;
Gilchrest, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (03) :1087-1092
[10]   THE VALIDITY AND PRACTICALITY OF SUN-REACTIVE SKIN TYPE-I THROUGH TYPE-VI [J].
FITZPATRICK, TB .
ARCHIVES OF DERMATOLOGY, 1988, 124 (06) :869-871