Abstract
In the present study, we investigated that (-)-aptosimon, isolated from flower buds of Daphne genkwa, inhibited cyclooxygenase-2 (COX-2) and inducible nitric oxide (NO) synthase (iNOS) expression in lipopolysaccharide (LPS)-stimulated RAW264.7 cells. Similarly, (-)-aptosimon suppressed tumor necrosis factor (TNF)-alpha production. Our results clearly indicated that (-)-aptosimon inhibited LPS-induced nuclear factor-kappaB (NF-kappaB) activation, by preventing degradation of the inhibitor kappa B-alpha (IkappaB-alpha). (-)-Aptosimon also inhibited interleukin-4 (IL-4) and interleukin-13 (IL-13) production in ConA-induced splenocytes. In conclusion, the anti-inflammatory effects of (-)-aptosimon are attributed to the suppression of pro-inflammatory cytokines and mediators by blocking NF-kappaB activation. These data suggest that (-)-aptosimon as a potential therapeutic agent for inflammation-associated disorders.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
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Cell Line
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Concanavalin A / metabolism
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Cyclooxygenase 2 / genetics
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Cyclooxygenase 2 / metabolism
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Daphne*
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Dioxoles / pharmacology*
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Enzyme Activation / drug effects
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Enzyme Activation / immunology
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Flowers
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Furans / pharmacology*
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Interleukin-13 / genetics
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Interleukin-13 / metabolism
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Interleukin-4 / genetics
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Interleukin-4 / metabolism
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Lipopolysaccharides / metabolism
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Macrophages / drug effects*
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Macrophages / immunology
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Macrophages / metabolism
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Macrophages / pathology
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Mice
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NF-kappa B / antagonists & inhibitors
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Nitric Oxide Synthase Type II / genetics
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Nitric Oxide Synthase Type II / metabolism
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Phytotherapy / trends*
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Transcriptional Activation / drug effects
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Tumor Necrosis Factor-alpha / genetics
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Tumor Necrosis Factor-alpha / metabolism
Substances
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Anti-Inflammatory Agents, Non-Steroidal
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Dioxoles
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Furans
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Interleukin-13
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Lipopolysaccharides
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NF-kappa B
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Tumor Necrosis Factor-alpha
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Concanavalin A
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Interleukin-4
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aptosimon
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Nitric Oxide Synthase Type II
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Nos2 protein, mouse
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Ptgs2 protein, mouse
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Cyclooxygenase 2