In vitro inhibition of Helicobacter pylori urease: biochemical and ultrastructural analysis

Eur J Clin Invest. 1991 Oct;21(5):551-7. doi: 10.1111/j.1365-2362.1991.tb01409.x.

Abstract

Inhibition of H. pylori urease was studied by means of electron-microscopy and electrophoretic methods using different urease inhibitors, such as acetohydroxamic-acid (AHA), L-ascorbic acid (AsA), copper ions, a combination of L-ascorbic acid with copper ions and UV light. AHA in two different concentrations and AsA at a concentration of 0.1 mg ml-1 showed incomplete inhibition of H. pylori urease activity in our electrophoretic experiments. Only membrane-bound activity was inhibited with AHA but not the activity localized within the cytoplasma as demonstrated by electron-microscopy. AsA at a concentration of 0.5 mg ml-1 and the combination of copper ions (1 microgram ml-1) with AsA completely inhibited the urease activity as demonstrated by electron-microscopy and electrophoretic experiments. Cu2+ ions in high concentrations (100 micrograms ml-1) and UV light exposure for more than 4 h induced a complete disintegration of H. pylori. Electrophoresis showed no active protein after UV light exposure of 2 h. Different urease inhibitors tested in this study showed dose-dependent inhibitory effects on H. pylori urease in vitro.

MeSH terms

  • Ascorbic Acid / pharmacology
  • Copper / pharmacology
  • Helicobacter pylori / drug effects
  • Helicobacter pylori / enzymology*
  • Helicobacter pylori / ultrastructure
  • Hydroxamic Acids / pharmacology
  • Microscopy, Electron
  • Ultraviolet Rays
  • Urease / antagonists & inhibitors*
  • Urease / radiation effects

Substances

  • Hydroxamic Acids
  • acetohydroxamic acid
  • Copper
  • Urease
  • Ascorbic Acid