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Wolf, P; Yarosh, DB; Kripke, ML.
Effects of sunscreens and a DNA excision repair enzyme on ultraviolet radiation-induced inflammation, immune suppression, and cyclobutane pyrimidine dimer formation in mice.
J Invest Dermatol. 1993; 101(4):523-527 Doi: 10.1111/1523-1747.ep12365902 [OPEN ACCESS]
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Leading authors Med Uni Graz
Wolf Peter
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Abstract:
Exposure of skin to ultraviolet (UV) radiation inhibits the induction of delayed-type hypersensitivity (DTH) responses initiated at a distant, unirradiated site. Recent studies attributed this form of immune suppression to DNA damage in the form of cyclobutane pyrimidine dimers (CPD). In the present study, we investigated the protective defects of sunscreens on UV-induced systemic suppression of DTH to Candida albicans, inflammation, and DNA damage. The photoprotective effects of sunscreen preparations containing 8% octyl-N-dimethyl-p-aminobenzoate, 7.5% 2-ethylhexyl-p-methoxycinnamate, or 6% benzophenone-3 were studied in C3H mice exposed to a single dose of 500 mJ/cm2 UVB radiation from FS40 sunlamps. Inflammation was determined by the amount of skin edema at the site of UV irradiation, and DNA damage was assessed by measuring the frequency of endonuclease-sensitive sites in the epidermis. Application of the sunscreens before UV irradiation gave 75-97% protection against UV-induced edema, 67-91% protection against formation of CPD, but only 30-54% protection against suppression of DTH. In contrast, the topical application of liposomes containing a CPD-specific DNA repair enzyme immediately after UV irradiation resulted in 82% protection against suppression of DTH, but at best, 39% protection against skin edema. These findings demonstrate that sunscreens give less protection against UV-induced immune suppression than against skin edema and CPD formation. Furthermore, they suggest that less DNA damage is required to cause UV-induced immune suppression than to cause sunburn.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
DNA Ligases - pharmacology
Deoxyribonuclease (Pyrimidine Dimer) - pharmacology
Dermatitis - etiology
Drug Carriers - etiology
Endodeoxyribonucleases - administration and dosage
Female - administration and dosage
Hypersensitivity, Delayed - prevention and control
Immunosuppression - prevention and control
Liposomes - prevention and control
Mice - prevention and control
Mice, Inbred C3H - prevention and control
Pyrimidine Dimers - biosynthesis
Radiation Injuries, Experimental - biosynthesis
Research Support, Non-U.S. Gov't - biosynthesis
Research Support, U.S. Gov't, P.H.S. - biosynthesis
Skin - metabolism
Sunscreening Agents - pharmacology
Ultraviolet Rays - pharmacology

Find related publications in this database (Keywords)
DELAYED-TYPE HYPERSENSITIVITY
DNA DAMAGE
LIPOSOMES
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