Suppression of NF-kappaB activation and cytokine production by N-acetylcysteine in pancreatic acinar cells

Free Radic Biol Med. 2000 Oct 1;29(7):674-83. doi: 10.1016/s0891-5849(00)00368-3.

Abstract

Reactive oxygen species (ROS), generated by infiltrating neutrophils, are considered as an important regulator in the pathogenesis and development of pancreatitis. A hallmark of the inflammatory response is the induction of cytokine gene expression, which may be regulated by oxidant-sensitive transcription factor, nuclear factor-kappaB (NF-kappaB). Present study aims to investigate whether neutrophils primed by 4beta-phorbol 12beta-myristate 13alpha-acetate (PMA) affect the productions of H(2)O(2) and lipid peroxide (LPO), NF-kappaB activation and cytokine production in pancreatic acinar cells, and whether these alterations were inhibited by N-acetylcysteine (NAC) and superoxide dismutase (SOD). Neutrophils generated ROS by stimulation with PMA, which was inhibited by NAC and SOD. In acinar cells, PMA-primed neutrophils increased the productions of H(2)O(2), LPO, and cytokines both time and dose dependently. PMA-primed neutrophils resulted in the activation of two species of NF-kappaB dimers (a p50/p65 heterodimer and a p50 homodimer) in acinar cells. Both NAC and SOD inhibited neutrophil-induced, oxidant-mediated alterations in acinar cells. In conclusion, ROS, generated by neutrophils, activates NF-kappaB, resulting in upregulation of inflammatory cytokines in acinar cells. Antioxidants such as NAC might be useful antiinflammatory agents by inhibiting oxidant-mediated activation of NF-kappaB and decreasing cytokine production.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcysteine / pharmacology*
  • Animals
  • Antioxidants / pharmacology*
  • Cells, Cultured
  • Cytokines / analysis
  • Cytokines / genetics*
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology*
  • Hydrogen Peroxide / metabolism
  • Kinetics
  • Lipid Peroxidation / drug effects*
  • Male
  • NF-kappa B / antagonists & inhibitors*
  • Pancreas / drug effects
  • Pancreas / immunology
  • Pancreas / physiology*
  • RNA, Messenger / genetics
  • Rats
  • Rats, Sprague-Dawley
  • Superoxide Dismutase / metabolism
  • Tetradecanoylphorbol Acetate / pharmacology
  • Time Factors
  • Transcription, Genetic / drug effects

Substances

  • Antioxidants
  • Cytokines
  • NF-kappa B
  • RNA, Messenger
  • Hydrogen Peroxide
  • Superoxide Dismutase
  • Tetradecanoylphorbol Acetate
  • Acetylcysteine