Curcumin attenuates inflammatory responses by suppressing TLR4-mediated NF-κB signaling pathway in lipopolysaccharide-induced mastitis in mice

Int Immunopharmacol. 2014 May;20(1):54-8. doi: 10.1016/j.intimp.2014.01.024. Epub 2014 Feb 6.

Abstract

Curcumin, the main constituent of the spice turmeric, has been reported to have potent anti-inflammatory properties. However, the effect of curcumin on lipopolysaccharide (LPS)-induced mice mastitis has not been investigated. The aim of this study was to investigate whether curcumin could ameliorate the inflammation response in LPS-induced mice mastitis and to clarify the possible mechanism. The mouse model of mastitis was induced by injection of LPS through the duct of the mammary gland. Curcumin was applied 1h before and 12h after LPS treatment. The results showed that curcumin attenuated the infiltration of inflammatory cells, the activity of myeloperoxidase (MPO), and the expression of tumor necrosis factor-α (TNF-α), interleukin-6 (IL-6) and interleukin-1β (IL-1β) in a dose-dependent manner. Additionally, Western blotting results showed that curcumin inhibited the phosphorylation of IκB-α and NF-κB p65 and the expression of TLR4. These results indicated that curcumin has protective effect on mice mastitis and the anti-inflammatory mechanism of curcumin on LPS-induced mastitis in mice may be due to its ability to inhibit TLR4-mediated NF-κB signaling pathways. Curcumin may be a potential therapeutic agent against mastitis.

Keywords: Curcumin; Mastitis; Myeloperoxidase; Nuclear factor-kappa B (NF-κB); TLR4.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology*
  • Anti-Inflammatory Agents / therapeutic use
  • Curcumin / pharmacology*
  • Curcumin / therapeutic use
  • Cytokines / immunology
  • Female
  • Lipopolysaccharides
  • Male
  • Mammary Glands, Animal / drug effects
  • Mammary Glands, Animal / immunology
  • Mammary Glands, Animal / pathology
  • Mastitis / chemically induced
  • Mastitis / drug therapy
  • Mastitis / immunology*
  • Mastitis / pathology
  • Mice, Inbred BALB C
  • NF-kappa B / immunology*
  • Peroxidase / immunology
  • Signal Transduction / drug effects
  • Toll-Like Receptor 4 / immunology*

Substances

  • Anti-Inflammatory Agents
  • Cytokines
  • Lipopolysaccharides
  • NF-kappa B
  • Tlr4 protein, mouse
  • Toll-Like Receptor 4
  • Peroxidase
  • Curcumin