| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5832124 | International Immunopharmacology | 2015 | 8 Pages |
â¢Fisetin induced HO-1 mRNA and protein expression in human keratinocyte HaCaT.â¢Fisetin prevented hydrogen peroxide-induced oxidative toxicity and ROS generation.â¢Fisetin suppressed inflammatory mediator, cytokine and protein via NF-κB signaling.â¢Fisetin increased Nrf2-mediated HO-1 expression via the PI3K/AKT cascade.â¢Fisetin can be potential used for the prevention of functional keratinocyte damage.
Oxidative skin damage and skin inflammation play key roles in the pathogenesis of skin-related diseases. Fisetin is a naturally occurring flavonoid abundantly found in several vegetables and fruits. Fisetin has been shown to exert various positive biological effects, such as anti-cancer, anti-proliferative, neuroprotective and anti-oxidative effects. In this study, we investigate the skin protective effects and anti-inflammatory properties of fisetin in hydrogen peroxide- and TNF-α-challenged human keratinocyte HaCaT cells. When HaCaT cells were treated with non-cytotoxic concentrations of fisetin (1-20 μM), heme oxygenase (HO)-1 mRNA and protein expression increased in a dose-dependent manner. Furthermore, fisetin dose-dependently increased cell viability and reduced ROS production in hydrogen peroxide-treated HaCaT cells. Fisetin also inhibited the production of NO, PGE2 IL-1β, IL-6, expression of iNOS and COX-2, and activation of NF-κB in HaCaT cells treated with TNF-α. Fisetin induced Nrf2 translocation to the nuclei. HO-1 siRNA transient transfection reversed the effects of fisetin on cytoprotection, ROS reduction, NO, PGE2, IL-1β, IL-6, and TNF-α production, and NF-κB DNA-binding activity. Moreover, fisetin increased Akt phosphorylation and a PI3K pathway inhibitor (LY294002) abolished fisetin-induced cytoprotection and NO inhibition. Taken together, these results provide evidence for a beneficial role of fisetin in skin therapy.
