The Modulatory Effect of Ellagic Acid and Rosmarinic Acid on Ultraviolet-B-Induced Cytokine/Chemokine Gene Expression in Skin Keratinocyte (HaCaT) Cells
Author(s) -
Serena Lembo,
Anna Balato,
Roberta Di Caprio,
Teresa Cirillo,
Valentina Giannini,
F Gasparri,
Giuseppe Monfrecola
Publication year - 2014
Publication title -
biomed research international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 126
eISSN - 2314-6141
pISSN - 2314-6133
DOI - 10.1155/2014/346793
Subject(s) - hacat , chemokine , rosmarinic acid , cytokine , chemistry , proinflammatory cytokine , gene expression , keratinocyte , ellagic acid , microbiology and biotechnology , tumor necrosis factor alpha , pharmacology , inflammation , immunology , biology , biochemistry , gene , in vitro , polyphenol , antioxidant
Ultraviolet radiation (UV) induces an increase in multiple cutaneous inflammatory mediators. Ellagic acid (EA) and rosmarinic acid (RA) are natural anti-inflammatory and immunomodulatory compounds found in many plants, fruits, and nuts. We assessed the ability of EA and RA to modulate IL-1 β , IL-6, IL-8, IL-10, MCP-1, and TNF- α gene expression in HaCaT cells after UVB irradiation. Cells were treated with UVB (100 mJ/cm 2 ) and simultaneously with EA (5 μ M in 0.1% DMSO) or RA (2.7 μ M in 0.5% DMSO). Moreover, these substances were added to the UVB-irradiated cells 1 h or 6 h before harvesting, depending on the established UVB-induced cytokine expression peak. Cytokine gene expression was examined using quantitative real time polymerase chain reaction. RA produced a significant reduction in UVB-induced expression of IL-6, IL-8, MCP-1, and TNF- α when applied at the same time as irradiation. EA showed milder effects compared with RA, except for TNF- α . Both substances decreased IL-6 expression, also when applied 5 h after irradiation, and always produced a significant increase in UVB-induced IL-10 expression. Our findings suggest that EA and RA are able to prevent and/or limit the UVB-induced inflammatory cascade, through a reduction in proinflammatory mediators and the enhancement of IL-10, with its protective function.
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