Photoprotective properties of Prunella vulgaris and rosmarinic acid on human keratinocytes
Language English Country Switzerland Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
16631374
DOI
10.1016/j.jphotobiol.2006.02.012
PII: S1011-1344(06)00075-3
Knihovny.cz E-resources
- MeSH
- Apoptosis drug effects radiation effects MeSH
- Cell Line MeSH
- Cinnamates pharmacology MeSH
- Depsides MeSH
- Photobiology MeSH
- Keratinocytes cytology drug effects metabolism radiation effects MeSH
- Rosmarinic Acid MeSH
- Humans MeSH
- Oxidative Stress drug effects radiation effects MeSH
- DNA Damage drug effects MeSH
- Cell Proliferation drug effects radiation effects MeSH
- Prunella * MeSH
- Radiation-Protective Agents pharmacology MeSH
- Plant Extracts pharmacology MeSH
- Ultraviolet Rays adverse effects MeSH
- Cell Survival drug effects radiation effects MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cinnamates MeSH
- Depsides MeSH
- Radiation-Protective Agents MeSH
- Plant Extracts MeSH
UVA radiation provokes the generation of reactive oxygen species (ROS), which induce oxidative stress in the exposed cells leading to extensive cellular damage and cell death either by apoptosis or necrosis. One approach to protecting human skin against the harmful effects of UV radiation is by using herbal compounds as photoprotectants. This study evaluated the protective effects of Prunella vulgaris L. (Labiatae) and its main phenolic acid component, rosmarinic acid (RA), against UVA-induced changes in a human keratinocyte cell line (HaCaT). Human keratinocytes exposed to UVA (10-30 J/cm(2)) were treated with an extract of P. vulgaris (1-75 mg/l) or RA (0.9-18 mg/l) for 4h. P. vulgaris and RA exhibited ability to reduce the UVA-caused decrease in a cell viability monitored by neutral red retention and by LDH release into medium. The P. vulgaris extract and RA significantly suppressed UVA-induced ROS production, which manifests as a decrease in intracellular lipid peroxidation, elevation of ATP and reduced glutathione. Post-treatment with P. vulgaris extract and RA also significantly reduced DNA damage. In addition, UVA-induced activation of caspase-3 was inhibited by treatment with P. vulgaris and RA. The P. vulgaris extract and RA demonstrated a concentration-dependent photoprotection (maximum at 25-50 mg/l and 9 mg/l, respectively). These results suggest that P. vulgaris and RA, used in skin care cosmetics, may offer protection against UVA-induced oxidative stress and may be beneficial as a supplement in photoprotective dermatological preparations.
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