Sauchinone suppresses pro-inflammatory mediators by inducing heme oxygenase-1 in RAW264.7 macrophages

Biol Pharm Bull. 2011;34(10):1566-71. doi: 10.1248/bpb.34.1566.

Abstract

Sauchinone, a biologically active lignan isolated from the roots of Saururus chinensis (LOUR.) BAILL. (Saururaceae), is reported to exert a variety of biological activities, such as hepatoprotective, anti-inflammatory actions and inhibitory effects on bone resorption. In this study, we investigated the effect of sauchinone in suppressing cyclooxygenase-2 (COX-2) and inducible nitric oxide synthase (iNOS) expression, leading to a reduction in COX-2-derived prostaglandin E(2) (PGE(2)) and iNOS-derived nitric oxide (NO) production in lipopolysaccharide (LPS) stimulated RAW264.7 macrophages. Present study also demonstrates the effects of sauchinone in inducing heme oxygenase-1 (HO-1) expression and an increase in heme oxygenase (HO) activity in RAW264.7 macrophages. The effects of sauchinone on LPS-induced PGE(2), NO, tumor necrosis factor-α (TNF-α) and interlukine-1β (IL-1β) production were partially reversed by the HO-1 inhibitor Tin protoporphyrin was also seen in this study. In addition, we found that treatment with extracellular signal-regulated kinase (ERK) inhibitor (PD98059) reduced sauchinone-induced HO-1 expression. Sauchinone also increased ERK phosphorylation. These results suggest that sauchinone inhibits pro-inflammatory mediators through expression of anti-inflammatory HO-1 via ERK pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / immunology
  • Anti-Inflammatory Agents / metabolism
  • Anti-Inflammatory Agents / pharmacology*
  • Benzopyrans / chemistry
  • Benzopyrans / immunology
  • Benzopyrans / metabolism
  • Benzopyrans / pharmacology*
  • Cell Line
  • Cyclooxygenase 2 / immunology
  • Cyclooxygenase 2 / metabolism
  • Dioxoles / chemistry
  • Dioxoles / immunology
  • Dioxoles / metabolism
  • Dioxoles / pharmacology*
  • Drug Evaluation, Preclinical
  • Enzyme Inhibitors / metabolism
  • Enzyme Inhibitors / pharmacology
  • Extracellular Signal-Regulated MAP Kinases / drug effects
  • Extracellular Signal-Regulated MAP Kinases / immunology
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Flavonoids / metabolism
  • Flavonoids / pharmacology
  • Heme Oxygenase-1 / immunology
  • Heme Oxygenase-1 / metabolism
  • Inflammation / drug therapy*
  • Inflammation / physiopathology
  • Inflammation Mediators / antagonists & inhibitors*
  • Inflammation Mediators / immunology
  • Lipopolysaccharides / immunology
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Macrophages / immunology
  • Metalloporphyrins
  • Mice
  • Molecular Targeted Therapy
  • Nitric Oxide / biosynthesis
  • Nitric Oxide / immunology
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / drug effects
  • Phosphorylation / drug effects
  • Phytotherapy
  • Plant Preparations / chemistry
  • Plant Preparations / isolation & purification
  • Plant Preparations / pharmacology*
  • Plant Roots
  • Protoporphyrins
  • Saururaceae*
  • Signal Transduction / drug effects
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / immunology

Substances

  • Anti-Inflammatory Agents
  • Benzopyrans
  • Dioxoles
  • Enzyme Inhibitors
  • Flavonoids
  • Inflammation Mediators
  • Lipopolysaccharides
  • Metalloporphyrins
  • Plant Preparations
  • Protoporphyrins
  • Tumor Necrosis Factor-alpha
  • sauchinone
  • Nitric Oxide
  • tin protoporphyrin IX
  • NOS2 protein, human
  • Nitric Oxide Synthase Type II
  • Heme Oxygenase-1
  • Cyclooxygenase 2
  • Extracellular Signal-Regulated MAP Kinases
  • 2-(2-amino-3-methoxyphenyl)-4H-1-benzopyran-4-one