Tectorigenin inhibits IFN-gamma/LPS-induced inflammatory responses in murine macrophage RAW 264.7 cells

Arch Pharm Res. 2008 Nov;31(11):1447-56. doi: 10.1007/s12272-001-2129-7. Epub 2008 Nov 21.

Abstract

Tectorigenin (Tg) and tectoridin (Td) are the major compounds isolated from the rhizomes of iridaceous plant Belamcanda chinensis which is well known as a chinese traditional medicine for the treatment of inflammatory diseases. In this study we investigated whether tectorigenin and tectoridin can be applied to the suppression of interferon-gamma and lipopolysaccharide (IFN-gamma/LPS)-induced inflammatory responses in macrophages. Anti-inflammatory activities of tectorigenin and tectoridin were compared with genistein (Ge), well known isoflavonoid as a phytoestrogen and regarded as an emerging anti-inflammatory agent. Both compounds showed low cytotoxic effect. In Raw 264.7 cells activated with IFN-gamma/LPS, pre-treated tectorigenin was found to inhibit the expression of inducible nitric oxide synthase (iNOS), the production of nitric oxide (NO) and the secretion of interleukin (IL)-1beta dose-dependently. Tectorigenin also decreased the expression of cyclooxigenase (COX)-2 and the production of prostaglandin E(2) (PGE(2)) in dose-dependent manner. These inhibitory effects of tectorigenin were found to be caused by the blocking of nuclear factor kappa-B (NF-kappaB) activation. Compared with genistein and tectoridin, tectorigenin showed significant inhibitory effect for almost anti-inflammatory tests in this study. All these results clearly demonstrated that tectorigenin appears to have the potential to prevent inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Blotting, Western
  • Cell Line
  • Cyclooxygenase 2 / metabolism
  • Dinoprostone / metabolism
  • Enzyme-Linked Immunosorbent Assay
  • Genistein / pharmacology
  • I-kappa B Kinase / metabolism
  • Indicators and Reagents
  • Interferon-gamma / antagonists & inhibitors*
  • Interleukin-1beta / metabolism
  • Isoflavones / pharmacology*
  • Lipopolysaccharides / antagonists & inhibitors*
  • Macrophages / drug effects
  • Macrophages / pathology*
  • Mice
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Phytoestrogens / pharmacology
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Indicators and Reagents
  • Interleukin-1beta
  • Isoflavones
  • Lipopolysaccharides
  • Phytoestrogens
  • Tumor Necrosis Factor-alpha
  • Nitric Oxide
  • Interferon-gamma
  • tectorigenin
  • tectoridin
  • Genistein
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2
  • I-kappa B Kinase
  • Dinoprostone