Reduction of acute photodamage in skin by topical application of a novel PARP inhibitor

被引:45
作者
Farkas, B
Magyarlaki, M
Csete, B
Nemeth, J
Rabloczky, G
Bernath, S
Nagy, PL
Sümegi, B
机构
[1] Univ Pecs, Fac Med, Dept Dermatol, H-7624 Pecs, Hungary
[2] Univ Pecs, Fac Med, Dept Pharmacol, H-7624 Pecs, Hungary
[3] Univ Pecs, Fac Med, Dept Biochem, H-7624 Pecs, Hungary
[4] N Gene Res Labs Inc, Budapest, Hungary
关键词
photodamage; PARP-inhibitor; poly-ADP-ribosylation; DNA damage; immunosuppression; photoprotection;
D O I
10.1016/S0006-2952(01)00929-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The ultraviolet (UV) components of sunlight induce damage to the DNA in skin cells, which is considered to be the initiating step in the harmful biological effects of UV radiation. Repair of DNA damage results in the formation of single-strand DNA breaks, which activate the nuclear poly(ADP-ribose) polymerase WARP). Overactivation of PARP worsens the oxidative cell damage and impairs the energy metabolism, raising the possibility that moderation of PARP activation following DNA damage may protect skin cells from UV radiation. The topical effects of the novel PARP inhibitor O-(3-pyperidino-2-hydroxy-1-propyl) pyridine-3-carboxylic acid amidoxime monohydrochloride (BGP-15M) were investigated on UV-induced skin damage in a hairless mouse model. For evaluation of the UV-induced acute photodamage to the skin and the potential protective effect of BGP-15M, DNA injury was detected by measuring the formation of single-strand DNA breaks and counting the resulting sunburn (apoptotic) cells. The ADP-ribosylation of PARP was assessed by Western blot analysis and then quantified. In addition, the UV-induced immunosuppression was investigated by the immunostaining of tumor necrosis factor alpha and interleukin-10 expressions in epidermal cells. The signs of inflammation were examined clinically and histochemically. Besides its primary effect in decreasing the activity of nuclear PARP, topically applied BGP-15M proved to be protective against solar and artificial UV radiation-induced acute skin damage. The DNA injury was decreased (P < 0.01). An inhibition of immunosuppression was observed by down-regulation of the epidermal production of cytokines IL-10 and TNFalpha. In the mouse skin, clinical or histological signs of UV-induced inflammation could not be observed. These data suggest that BGP-15M directly interferes with UV-induced cellular processes and modifies the activity of PARR The effects provided by topical application of the new PARP-regulator BGP-15M indicate that it may be a novel type of agent in photoprotection of the skin. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:921 / 932
页数:12
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