Oxidative damage to nucleic acids and benzo(a)pyrene-7,8-diol-9,10-epoxide-DNA adducts and chromosomal aberration in children with psoriasis repeatedly exposed to crude coal tar ointment and UV radiation
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25197429
PubMed Central
PMC4146480
DOI
10.1155/2014/302528
Knihovny.cz E-resources
- MeSH
- 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide analysis chemistry MeSH
- DNA Adducts analysis chemistry MeSH
- Benzo(a)pyrene chemistry toxicity MeSH
- Chromosome Aberrations * MeSH
- Coal Tar pharmacology therapeutic use MeSH
- Child MeSH
- DNA chemistry MeSH
- Keratolytic Agents pharmacology therapeutic use MeSH
- Cohort Studies MeSH
- Humans MeSH
- Lymphocytes cytology metabolism MeSH
- Ointments pharmacology therapeutic use MeSH
- Adolescent MeSH
- Oxidative Stress drug effects MeSH
- DNA Damage drug effects MeSH
- Child, Preschool MeSH
- Prospective Studies MeSH
- Psoriasis drug therapy metabolism pathology MeSH
- Ultraviolet Rays * MeSH
- Check Tag
- Child MeSH
- Humans MeSH
- Adolescent MeSH
- Male MeSH
- Child, Preschool MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide MeSH
- DNA Adducts MeSH
- benzo(a)pyrene-7,8-dihydrodiol-9,10-epoxide-DNA MeSH Browser
- Benzo(a)pyrene MeSH
- Coal Tar MeSH
- DNA MeSH
- Keratolytic Agents MeSH
- Ointments MeSH
The paper presents a prospective cohort study. Observed group was formed of children with plaque psoriasis (n=19) treated by Goeckerman therapy (GT). The study describes adverse (side) effects associated with application of GT (combined exposure of 3% crude coal tar ointment and UV radiation). After GT we found significantly increased markers of oxidative stress (8-hydroxy-2'-deoxyguanosine, 8-hydroxyguanosine, and 8-hydroxyguanine), significantly increased levels of benzo[a]pyrene-7,8-diol-9,10-epoxide (BPDE) DNA adducts (BPDE-DNA), and significantly increased levels of total number of chromosomal aberrations in peripheral lymphocytes. We found significant relationship between (1) time of UV exposure and total number of aberrated cells and (2) daily topical application of 3% crude coal tar ointment (% of body surface) and level of BPDE-DNA adducts. The findings indicated increased hazard of oxidative stress and genotoxic effects related to the treatment. However, it must be noted that the oxidized guanine species and BPDE-DNA adducts also reflect individual variations in metabolic enzyme activity (different extent of bioactivation of benzo[a]pyrene to BPDE) and overall efficiency of DNA/RNA repair system. The study confirmed good effectiveness of the GT (significantly decreased PASI score).
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