Celecoxib inhibits Helicobacter pylori colonization-related factors

World J Gastroenterol. 2010 Feb 21;16(7):846-53. doi: 10.3748/wjg.v16.i7.846.

Abstract

Aim: To investigate the effect of celecoxib, a selective COX-2 inhibitor, on Helicobacter pylori (H. pylori) colonization-related factors and its mechanism.

Methods: After co-incubation with celecoxib, morphology of H. pylori strain 26695 was observed under a transmission electron microscope. Flagella motility was assessed by stab agar motility test. Adherence of H. pylori to AGS cells was determined by enzyme linked immunosorbent assay. Levels of mRNA expression in flagellar genes (flaA, flaB), urease genes (ureA, ureB) and adhesin genes (babA, sabA, alpA, alpB, hpaA, hopZ) were measured by real-time polymerase chain reaction.

Results: Separation and non-integrity of bacterial cell wall, rarefaction and asymmetry of cytoplasm, and even lysis of H. pylori were observed in the presence of celecoxib. When H. pylori strains were incubated in the presence of celecoxib, their flagellar motility and adherence to AGS cells were inhibited. The expression of ureA, ureB, babA, sabA, alpA, alpB, hpaA, hopZ was up-regulated while the expression of flaA, flaB was down-regulated in the presence of celecoxib.

Conclusion: Celecoxib inhibits flagellar motility and adherence of H. pylori to AGS cells, and destructs their normal structure in vitro.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adhesins, Bacterial / genetics
  • Bacterial Adhesion / drug effects
  • Celecoxib
  • Cell Line, Tumor
  • Cyclooxygenase 2 Inhibitors / pharmacology*
  • Dose-Response Relationship, Drug
  • Enzyme-Linked Immunosorbent Assay
  • Flagella / drug effects
  • Flagella / ultrastructure
  • Flagellin / genetics
  • Gastric Mucosa / drug effects*
  • Gastric Mucosa / microbiology
  • Gastric Mucosa / pathology
  • Gene Expression Regulation, Bacterial / drug effects
  • Helicobacter pylori / drug effects*
  • Helicobacter pylori / genetics
  • Helicobacter pylori / growth & development
  • Helicobacter pylori / pathogenicity
  • Helicobacter pylori / ultrastructure
  • Humans
  • Microscopy, Electron, Transmission
  • Movement
  • Pyrazoles / pharmacology*
  • RNA, Bacterial / metabolism
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sulfonamides / pharmacology*
  • Urease / genetics

Substances

  • Adhesins, Bacterial
  • Cyclooxygenase 2 Inhibitors
  • Pyrazoles
  • RNA, Bacterial
  • RNA, Messenger
  • Sulfonamides
  • Flagellin
  • Urease
  • Celecoxib