Acute effects of Helicobacter pylori extracts on gastric mucosal blood flow in the mouse

World J Gastroenterol. 2009 Jan 14;15(2):219-25. doi: 10.3748/wjg.15.219.

Abstract

Aim: To investigate the mechanisms underlying the reduction in gastric blood flow induced by a luminal water extract of Helicobacter pylori (HPE).

Methods: The stomachs of isoflurane-anesthetized mice were exteriorized, and the mucosal surface exposed. Blood flow was measured with the laser-Doppler technique, and systemic arterial blood pressure monitored. C57BL/6 mice were exposed to water extract produced from H pylori strain 88-23. To investigate the role of a nerve- or iNOS-mediated pathway, we used intraluminal lidocaine and iNOS-/- mice. Blood flow response to the endogenous nitric oxide synthase inhibitor asymmetric dimethyl arginine (ADMA) was also assessed.

Results: In wild-type mice, HPE decreased mucosal blood flow by approximately 30%. This reduction was abolished in iNOS-deficient mice, and by pre-treatment with lidocaine. Luminally applied ADMA resulted in reduction in blood flow similar to that observed in wild-type mice exposed to HPE.

Conclusion: A H pylori water extract reduces gastric mucosal blood flow acutely through iNOS- and nerve-mediated pathways.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arginine / analogs & derivatives
  • Arginine / pharmacology
  • Blood Flow Velocity / drug effects
  • Gastric Mucosa / blood supply*
  • Gastric Mucosa / drug effects
  • Gastric Mucosa / innervation
  • Gastric Mucosa / microbiology*
  • Helicobacter pylori / chemistry
  • Helicobacter pylori / pathogenicity*
  • Lidocaine / pharmacology
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nitric Oxide Synthase Type II / deficiency
  • Nitric Oxide Synthase Type II / genetics
  • Nitric Oxide Synthase Type II / physiology
  • Signal Transduction / drug effects
  • Water

Substances

  • Water
  • N,N-dimethylarginine
  • Arginine
  • Lidocaine
  • Nitric Oxide Synthase Type II
  • Nos2 protein, mouse