Indole-3-carbinol inhibits LPS-induced inflammatory response by blocking TRIF-dependent signaling pathway in macrophages

Food Chem Toxicol. 2013 Jul:57:256-61. doi: 10.1016/j.fct.2013.03.040. Epub 2013 Apr 15.

Abstract

Indole-3-carbinol (I3C), a natural hydrolysis product of glucobrassicin, is a member of the Brassica family of vegetables and is known to have various anti-cancer activities. In the present study, we assessed in vitro and in vivo anti-inflammatory effects of I3C and its molecular mechanisms. I3C attenuated the production of pro-inflammatory mediators such as NO, IL-6, and IL-1β in LPS-induced Raw264.7 cells and THP-1 cells through attenuation of the TRIF-dependent signaling pathway. Furthermore, I3C suppressed the infiltration of immune cells into the lung and pro-inflammatory cytokine production such as IL-6, TNF-α in broncho-alveolar lavage fluid (BALF) in the LPS-induced acute lung injury mouse model. I3C also suppressed IL-1β secretion in nigericin treated in vivo model. I3C has potent anti-inflammatory effects through regulating TRIF-dependent signaling pathways, suggesting that I3C may provide a valuable therapeutic strategy in treating various inflammatory diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / metabolism*
  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Bronchoalveolar Lavage Fluid / immunology
  • Cell Line / drug effects
  • Cytokines / metabolism
  • Disease Models, Animal
  • Female
  • Indoles / pharmacology*
  • Inflammation / drug therapy*
  • Inflammation / metabolism
  • Inflammation / pathology
  • Inflammation Mediators / metabolism
  • Lipopolysaccharides / pharmacology*
  • Macrophages / drug effects*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mice
  • Mice, Inbred BALB C
  • Myeloid Differentiation Factor 88 / metabolism
  • Nitric Oxide / metabolism
  • Pneumonia / drug therapy
  • Pneumonia / etiology
  • Pneumonia / pathology
  • Signal Transduction / drug effects

Substances

  • Adaptor Proteins, Vesicular Transport
  • Anti-Inflammatory Agents, Non-Steroidal
  • Cytokines
  • Indoles
  • Inflammation Mediators
  • Lipopolysaccharides
  • Myd88 protein, mouse
  • Myeloid Differentiation Factor 88
  • TICAM-1 protein, mouse
  • Nitric Oxide
  • indole-3-carbinol