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Phloroglucinol protects human keratinocytes from ultraviolet B radiation by attenuating oxidative stress
Author(s) -
Kim Ki Cheon,
Piao Mei Jing,
Cho Suk Ju,
Lee Nam Ho,
Hyun Jin Won
Publication year - 2012
Publication title -
photodermatology, photoimmunology and photomedicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.736
H-Index - 60
eISSN - 1600-0781
pISSN - 0905-4383
DOI - 10.1111/phpp.12010
Subject(s) - phloroglucinol , hacat , lipid peroxidation , superoxide dismutase , reactive oxygen species , chemistry , oxidative stress , keratinocyte , photoprotection , catalase , superoxide , human skin , antioxidant , biochemistry , dna damage , biology , enzyme , dna , in vitro , photosynthesis , organic chemistry , genetics
Summary Background Ultraviolet B generates reactive oxygen species by interacting with water in irradiated skin tissues and cells in turn causes lipid peroxidation, protein modification and further DNA damage. Purpose This study examined the cytoprotective effects of phloroglucinol (1,3,5‐trihydroxybenzene) on ultraviolet B ‐irradiated cultured human keratinocytes. Methods The human keratinocyte cell line HaCaT cells were treated with 10 μM of phloroglucinol. After 1 h, the cells were irradiated with ultraviolet B light at 30 mJ /cm 2 and incubated at 37° C . Results Phloroglucinol scavenged both the superoxide anion and hydroxyl radical in a cell‐free system and ultraviolet B ‐induced intracellular reactive oxygen species. Phloroglucinol reduced ultraviolet B ‐generated lipid peroxidation, protein modification and DNA strand breaks. The enzymatic effects of phloroglucinol restored cellular glutathione levels, superoxide dismutase and catalase activities, which were impaired by ultraviolet B radiation. Conclusion: Phloroglucinol provides the protective effects in human keratinocyte cell line exposed to ultraviolet B radiation, suggesting that phloroglucinol can be used as a photoprotective agent.
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