Protein kinase C-dependent stimulation of Na(+)-K(+)-ATP epsilon in rat proximal convoluted tubules

Am J Physiol. 1995 May;268(5 Pt 1):C1277-83. doi: 10.1152/ajpcell.1995.268.5.C1277.

Abstract

In rat proximal convoluted tubule (PCT), activation of protein kinase C (PKC) by phorbol 12,13-dibutyrate (PDBu) was previously reported to inhibit Na(+)-K(+)-ATPase, a paradoxical finding in view of the known stimulatory effect of PKC on Na+ reabsorption. Because this inhibition occurs via phospholipase A2 activation, a pathway stimulated by hypoxia, we evaluated the influence of oxygen supply on PKC action on Na(+)-K(+)-ATPase. Results confirmed that PDBu inhibited PCT Na(+)-K(+)-ATPase activity under usual conditions. In contrast, when oxygen supply was increased, PDBu had no effect on Na(+)-K(+)-ATPase hydrolytic activity, but it dose-dependently stimulated ouabain-sensitive 86Rb+ uptake. This latter effect, which was abolished by PKC inhibitors, resulted from an increment of the Na+ sensitivity of Na(+)-K(+)-ATPase. Thus, in oxygenated rat PCTs, activation of PKC primarily stimulated Na(+)-K(+)-ATPase. This likely contributes to increase solute reabsorption. Inhibition of Na(+)-K(+)-ATPase was observed only under hypoxic conditions. It may represent an adaptation to protect PCTs against deleterious effects of hypoxia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Enzyme Activation
  • Kidney Tubules, Proximal / enzymology*
  • Male
  • Ouabain / pharmacology
  • Oxygen / pharmacology
  • Phorbol 12,13-Dibutyrate / pharmacology
  • Protein Kinase C / physiology*
  • Rats
  • Rats, Wistar
  • Rubidium / pharmacokinetics
  • Sodium / metabolism
  • Sodium-Potassium-Exchanging ATPase / metabolism*

Substances

  • Phorbol 12,13-Dibutyrate
  • Ouabain
  • Sodium
  • Protein Kinase C
  • Sodium-Potassium-Exchanging ATPase
  • Rubidium
  • Oxygen