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Two natural flavonoids, quercetin and isorhamnetin 3-O-acylglucosides, were examined for their inhibitory influence on the in vitro production and release of reactive oxygen spe­cies in polymorphonuclear neutrophils (PMNs). The generation of superoxide radical, hy­drogen peroxide and hypochlorous acid were measured by, respectively, cytochrome c re­duction, dichlorofluorescin oxidation and taurine chlorination. Membrane lipid oxidation was studied by the thiobarbituric acid method in mouse spleen microsomes. The addition of flavonoids at the concentration range 1-100 uM inhibited PMNs oxidative metabolism and lipid peroxidation in a dose-dependent manner. The results suggest that these flavonoids suppress the oxidative burst of PMNs and protect membranes against lipid peroxidation.
Naturally occurring phenolics: protocatechuic, chlorogenic, tannic acids and trihydroxystilbene and resveratrol were shown to inhibit multistage carcinogenesis in animal models, including mouse epidermis. Treatment of mouse skin with tumor promoter 12-Otetradecanoyl phorbol-13-acetate (TPA) may induce ROS production in keratinocytes and skin infiltrating leukocytes. In our study, the effect of these phenolics on intracellular ROS production and DNA damage was examined. ROS were analysed by flow cytometry, while DNA damage by comet assay. Following treatment with TPA (6.8 nmol/mouse) two subpopulations of epidermal cells were identified. Pretreatment of mice with 16 mmol of phenolics decreased ROS production in both subpopulations. The most efficient inhibitors of ROS in whole population of keratinocytes were chlorogenic acid and resveratrol. Tannic acid reduced the most DNA damage induced by TPA treatment. These results suggest that anti-promotional effects of these two plant phenols might be partially explained by the inhibition of TPA-induced inflammation.
Silybin and silydianin exerted an inhibitory effect on superoxide radical production, peak chemiluminescence and hydrogen peroxide production in human polymorphonuclear neutrophils activated with opsonized zymosan.
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