Nicotine stimulates the expression of cyclooxygenase-2 mRNA via NFkappaB activation in human gingival fibroblasts

Arch Oral Biol. 2009 Mar;54(3):251-7. doi: 10.1016/j.archoralbio.2008.11.006. Epub 2009 Jan 14.

Abstract

Nicotine, a major component in tobacco smoke, stimulates the synthesis of prostaglandin E(2). We investigated the involvement of the transcription nuclear factor kappa B (NFkappaB) in the nicotine-induced expression of cyclooxygenase-2 (COX-2), a key enzyme for prostaglandin synthesis, in human gingival fibroblasts. Nicotine-stimulated release of prostaglandin E(2) and expression of COX-2 mRNA in a time- and dose-dependent manner. The nicotine-stimulated release of prostaglandin E(2) and expression of COX-2 mRNA and protein were inhibited by an NFkappaB inhibitor, pyrrolidine dithiocarbamate (PDTC), by approximately 50%. Nicotine stimulation of IkappaBalpha, an inhibitor of NFkappaB degradation, was also characterized by Western blotting. Mecamylamine, a specific antagonist of the nicotinic acetylcholine receptor, failed to inhibit the effect of nicotine on prostaglandin E(2) release. When human gingival fibroblasts were incubated with [3H]-nicotine, uptake of nicotine was observed. These results suggest that nicotine is taken up by human gingival fibroblasts and that it then stimulates COX-2 expression via the activation of NFkappaB and the subsequent release of prostaglandin E(2).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cells, Cultured
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism*
  • Dinoprostone / metabolism
  • Fibroblasts / drug effects*
  • Fibroblasts / metabolism
  • Gingiva / drug effects
  • Gingiva / metabolism*
  • Humans
  • Mecamylamine / pharmacology
  • NF-kappa B / genetics
  • NF-kappa B / metabolism*
  • Nicotine / antagonists & inhibitors
  • Nicotine / metabolism
  • Nicotine / pharmacology*
  • Nicotinic Antagonists / pharmacology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Transcriptional Activation

Substances

  • NF-kappa B
  • Nicotinic Antagonists
  • RNA, Messenger
  • Mecamylamine
  • Nicotine
  • Cyclooxygenase 2
  • Dinoprostone