Protective effect of ferulic acid ethyl ester against oxidative stress mediated by UVB irradiation in human epidermal melanocytes

被引:47
作者
Di Domenico, F. [1 ]
Perluigi, M. [1 ]
Foppoli, C. [2 ]
Blarzino, C. [1 ]
Coccia, R. [1 ]
De Marco, F. [3 ]
Butterfield, D. A. [4 ,5 ,6 ]
Cini, C. [1 ,2 ]
机构
[1] Univ Roma La Sapienza, Dept Biochem Sci, I-00185 Rome, Italy
[2] CNR, Inst Mol Biol & Pathol, I-00185 Rome, Italy
[3] Regina Elena Inst Canc Res, Virol Lab, I-00156 Rome, Italy
[4] Univ Kentucky, Dept Chem, Lexington, KY 40506 USA
[5] Univ Kentucky, Sanders Brown Ctr Aging, Lexington, KY 40506 USA
[6] Univ Kentucky, Ctr Membrane Sci, Lexington, KY 40506 USA
基金
美国国家卫生研究院;
关键词
UVB; oxidative stress; melanocytes; heme oxygenase-1; MICHAEL REACTION ACCEPTORS; HEAT-SHOCK-PROTEIN; NITRIC-OXIDE; ULTRAVIOLET-RADIATION; HEME OXYGENASE-1; ANTIOXIDANT PROPERTIES; NITRATED PROTEINS; IDENTIFICATION; EXPRESSION; DISEASE;
D O I
10.1080/10715760902777329
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
UV solar radiation is the major environmental risk factor for malignant melanoma. A great effort is currently posed on the search of new compounds able to prevent or reduce UV-mediated cell damage. Ferulic acid is a natural compound recently included in the formulation of solar protecting dermatological products. The purpose of the present work was to assess whether its ethyl ester derivative, FAEE, could protect skin melanocytes from UV-induced oxidative stress and cell damage. Experiments on human melanocytes irradiated with UVB showed that FAEE treatment reduced the generation of ROS, with a net decrease of protein oxidation. FAEE treatment was accompanied by an induction of HSP70 and heme oxygenase, by a marked suppression of PARP activation and a significant suppression of apoptosis. Moreover FAEE prevented iNOS induction, thus suppressing the secondary generation of NO-derived oxidizing agents. FAEE may represent a potentially effective pharmacological approach to reduce UV radiation-induced skin damage.
引用
收藏
页码:365 / 375
页数:11
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