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- W2064647661 abstract "In the present study, experiments were performed to explore the action of quercetin, the most widely distributed flavonoids, and its major metabolite, quercetin-3′-sulfate, on lipopolysaccharide (LPS)- and interferon-γ (IFN-γ)-induced nitric oxide (NO) production in BV-2 microglia. Quercetin could suppress LPS- and IFN-γ-induced NO production and inducible nitric oxide synthase (iNOS) gene transcription, while quercetin-3′-sulfate had no effect. LPS-induced IκB kinase (IKK), nuclear factor-κB (NF-κB) and activating protein-1 (AP-1) activation, and IFN-γ-induced NF-κB, signal transducer and activator of transcription-1 (STAT1) and interferon regulatory factor-1 (IRF-1) activation were reduced by quercetin. Moreover quercetin was able to induce heme oxygenase-1 expression. To address the involvement of heme oxygenase-1 induction in iNOS inhibition, heme oxygenase-1 antisense oligodeoxynucleotide was used. Quercetin-mediated inhibition of NO production and iNOS protein expression were partially reversed by heme oxygenase-1 antisense oligodeoxynucleotide, but was mimicked by hemin, a heme oxygenase-1 inducer. The involvement of signal pathways in quercetin-induced heme oxygenase-1 gene expression was associated with tyrosine kinase and mitogen-activated protein kinases activation. All these results suggest quercetin should provide therapeutic benefits for suppression of inflammatory-related neuronal injury in neurodegenerative diseases." @default.
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- W2064647661 date "2005-10-01" @default.
- W2064647661 modified "2023-10-15" @default.
- W2064647661 title "Inhibition of iNOS gene expression by quercetin is mediated by the inhibition of IκB kinase, nuclear factor-kappa B and STAT1, and depends on heme oxygenase-1 induction in mouse BV-2 microglia" @default.
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- W2064647661 doi "https://doi.org/10.1016/j.ejphar.2005.08.005" @default.
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