NEFAs activate the oxidative stress-mediated NF-κB signaling pathway to induce inflammatory response in calf hepatocytes

J Steroid Biochem Mol Biol. 2015 Jan:145:103-12. doi: 10.1016/j.jsbmb.2014.10.014. Epub 2014 Oct 22.

Abstract

Non-esterified fatty acids (NEFAs) are important induction factors of inflammatory responses in some metabolic diseases. High plasma levels of NEFAs and oxidative stress exist in the dairy cows with ketosis. The aim of this study was to investigate whether high levels of NEFAs can induce inflammatory response and the specific molecular mechanism in the hepatocytes of dairy cow. In vitro, primary cultured bovine hepatocytes were treated with different concentrations of NEFAs, PDTC (an NF-κB inhibitor) and NAC (an antioxidant). NEFAs significantly activated NF-κB pathway. Activated NF-κB upregulated the release of pro-inflammatory cytokines, thereby inducing inflammatory response in bovine hepatocytes. When PDTC was added, activation of NF-κB-mediated inflammatory response induced by NEFAs was inhibited. NEFAs treatment results in the overproduction of the markers of oxidative stress, reactive oxygen species (ROS) and malondialdehyde (MDA), which were ameliorated by NAC treatment. These increased ROS and MDA were caused by decreasing activity of antioxidant system, including glutathione peroxidase, superoxide dismutase and catalase, in bovine hepatocytes treated with NEFAs. NAC also ameliorated NEFAs-mediated NF-κB activation and the release of pro-inflammatory cytokines. These results indicate that high concentrations of NEFAs can induce cattle hepatocytes inflammatory response through activating the oxidative stress-mediated NF-κB signaling pathway.

Keywords: Bovine hepatocytes; Cow ketosis; Inflammatory injury; Non-esterified fatty acids; Oxidative stress.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Cattle
  • Cells, Cultured
  • Fatty Acids, Nonesterified / metabolism*
  • Female
  • Hepatocytes / drug effects
  • Hepatocytes / metabolism*
  • I-kappa B Kinase / metabolism
  • Inflammation
  • Interleukin-1beta / metabolism
  • Interleukin-6 / metabolism
  • Ketosis / pathology
  • NF-kappa B / metabolism*
  • Oxidative Stress*
  • Oxygen / metabolism
  • Phosphorylation
  • Reactive Oxygen Species / metabolism
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antioxidants
  • Fatty Acids, Nonesterified
  • Interleukin-1beta
  • Interleukin-6
  • NF-kappa B
  • Reactive Oxygen Species
  • Tumor Necrosis Factor-alpha
  • I-kappa B Kinase
  • Oxygen