Influence of COX-2 and local cytokine expressions in gastric ulcer mucosa by H. pylori and NSAID

Hepatogastroenterology. 2006 Sep-Oct;53(71):797-803.

Abstract

Background/aims: H. pylori and NSAIDs are the two most important pathogenic factors in gastric ulcer. NSAIDs and H. pylori share common pathogenic characteristics, but have different effects in modulating COX-2 and local cytokines in gastric ulcer mucosa. This study was designed to explore the influence of COX-2 and local cytokine expressions in gastric ulcer mucosa induced by H. pylori infection and NSAID use.

Methodology: Twenty-three patients were recruited. Sixteen subjects were infected with H. pylori. Fifteen patients used NSAIDs. Gastric biopsy specimens were obtained by endoscopy. COX-2 and local cytokine mRNA expressions were assessed by real-time RT-PCR.

Results: COX-2 and local cytokines were over-expressed in gastric ulcer and were positively intercorrelated. H. pylori did not alter COX-2 and local cytokine expressions in gastric ulcer, but induced IL-8 and COX-2 in antral mucosa. NSAIDs inhibited COX-2 expression in gastric ulcer, but had no effect on other local cytokines. COX-2 inhibition by NSAIDs in gastric ulcer was compatible with the findings that NSAIDs delayed gastric ulcer healing.

Conclusions: H. pylori increased IL-8 and COX-2 in the antral mucosa, but did not influence COX-2 and local cytokines in gastric ulcer. NSAIDs inhibited COX-2 in gastric ulcer and delayed gastric ulcer healing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Anti-Inflammatory Agents, Non-Steroidal / metabolism*
  • Cyclooxygenase 2 / metabolism*
  • Endoscopy, Gastrointestinal
  • Female
  • Helicobacter pylori*
  • Humans
  • Interleukin-4 / metabolism
  • Interleukin-8 / metabolism*
  • Intestinal Mucosa / metabolism*
  • Male
  • Membrane Proteins / metabolism*
  • Middle Aged
  • Prospective Studies
  • Pyloric Antrum / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Stomach Ulcer / drug therapy
  • Stomach Ulcer / metabolism*
  • Stomach Ulcer / physiopathology
  • Tumor Necrosis Factor-alpha / metabolism
  • Wound Healing

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Interleukin-8
  • Membrane Proteins
  • Tumor Necrosis Factor-alpha
  • Interleukin-4
  • Cyclooxygenase 2
  • PTGS2 protein, human