Modulation of gastric H+,K+-transporting ATPase function by sodium

FEBS Lett. 1985 Jun 3;185(1):24-8. doi: 10.1016/0014-5793(85)80733-x.

Abstract

Gastric H+,K+-ATPase activity is not affected by Na+ at pH 7.0 but is significantly stimulated by Na+ at pH 8.5. For the stimulation at the latter pH, the presence of both Na+ and K+ were essential. Contrary the H+,K+-ATPase, the associated K+-pNPPase was inhibited by Na+ at both pH values. Sodium competes with K+ for the K+-pNPPase reaction. Also, unlike the H+, K+-ATPase activity the ATPase-mediated transport of H+ within the gastric microsomal vesicles was inhibited by Na+. For the latter event only the extravesicular and not the intravesicular Na+ was effective. The data suggest that the K+-pNPPase activity does not represent the phosphatase step of the H+,K+-ATPase reaction. In addition, the observed inhibition of vesicular H+ uptake by Na+ appears to be due to the displacement by Na+ of a cytosolic (extravesicular) H+ site responsible for the vectorial translocation of H+.

MeSH terms

  • 4-Nitrophenylphosphatase* / antagonists & inhibitors
  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Binding, Competitive
  • Biological Transport / drug effects
  • H(+)-K(+)-Exchanging ATPase
  • Hydrogen-Ion Concentration
  • Microsomes / enzymology
  • Phosphoric Monoester Hydrolases* / antagonists & inhibitors
  • Protons
  • Sodium / pharmacology*
  • Stomach / enzymology*
  • Swine

Substances

  • Protons
  • Sodium
  • Phosphoric Monoester Hydrolases
  • 4-Nitrophenylphosphatase
  • Adenosine Triphosphatases
  • H(+)-K(+)-Exchanging ATPase