Helicobacter pylori fatty acid cis 9,10-methyleneoctadecanoic acid increases [Ca2+]i, activates protein kinase C and stimulates acid secretion in parietal cells

Prostaglandins Leukot Essent Fatty Acids. 1998 Aug;59(2):119-25. doi: 10.1016/s0952-3278(98)90090-4.

Abstract

The effect of the Helicobacter pylori (H. pylori) fatty acid cis 9,10-methyleneoctadecanoic acid (MOA) on gastric acid secretion was studied in isolated guinea-pig parietal cells. MOA (1 and 3 micromol/l) stimulated basal and enhanced histamine- and dibutyryl cyclic AMP-stimulated acid secretion in parietal cells. MOA increased intracellular free [Ca2+]i concentration in a concentration-dependent manner. The source of [Ca2+]i was extracellular as demonstrated by depletion of [Ca2+]i with EGTA. Furthermore, MOA caused activation of parietal cell protein kinase C (PKC). The effect of MOA upon PKC activation was [Ca2+]i-dependent but did not require phosphatidylserine as phospholipid co-factor. Similarly to the effect of diolein, MOA increased the stimulatory effect of phosphatidylserine at low [Ca2+]i concentrations. Treatment of parietal cells with MOA caused translocation of PKC from the cytosol to the membrane-associated cell fraction. We propose that MOA stimulates parietal cell acid secretion presumably by an increase of cytosolic free [Ca2+]i concentrations and PKC activation.

MeSH terms

  • 1-Methyl-3-isobutylxanthine / pharmacology
  • Aminopyrine / metabolism
  • Animals
  • Bucladesine / pharmacology
  • Calcium Signaling / drug effects*
  • Carbachol / pharmacology
  • Diglycerides / pharmacology
  • Enzyme Activation
  • Fatty Acids / analysis
  • Fatty Acids / pharmacology*
  • Gastric Acid / metabolism*
  • Guinea Pigs
  • Helicobacter pylori / chemistry*
  • Histamine / pharmacology
  • L-Lactate Dehydrogenase / metabolism
  • Parietal Cells, Gastric / drug effects
  • Parietal Cells, Gastric / metabolism*
  • Parietal Cells, Gastric / microbiology
  • Phosphatidylserines / pharmacology
  • Phosphodiesterase Inhibitors / pharmacology
  • Protein Kinase C / antagonists & inhibitors
  • Protein Kinase C / metabolism*
  • Staurosporine / pharmacology

Substances

  • Diglycerides
  • Fatty Acids
  • Phosphatidylserines
  • Phosphodiesterase Inhibitors
  • Aminopyrine
  • dihydrosterculic acid
  • Bucladesine
  • Histamine
  • Carbachol
  • L-Lactate Dehydrogenase
  • Protein Kinase C
  • Staurosporine
  • 1-Methyl-3-isobutylxanthine
  • diolein