Modulation of aldosterone-induced stimulation of ENaC synthesis by changing the rate of apical Na+ entry

Am J Physiol Renal Physiol. 2001 Oct;281(4):F687-92. doi: 10.1152/ajprenal.2001.281.4.F687.

Abstract

Primary cultures of immunodissected rabbit connecting tubule and cortical collecting duct cells were used to investigate the effect of apical Na+ entry rate on aldosterone-induced transepithelial Na+ transport, which was measured as benzamil-sensitive short-circuit current (I(sc)). Stimulation of the apical Na+ entry, by long-term short-circuiting of the monolayers, suppressed the aldosterone-stimulated benzamil-sensitive I(sc) from 320 +/- 49 to 117 +/- 14%, whereas in the presence of benzamil this inhibitory effect was not observed (335 +/- 74%). Immunoprecipitation of [(35)S]methionine-labeled beta-rabbit epithelial Na+ channel (rbENaC) revealed that the effects of modulation of apical Na+ entry on transepithelial Na+ transport are exactly mirrored by beta-rbENaC protein levels, because short-circuiting the monolayers decreased aldosterone-induced beta-rbENaC protein synthesis from 310 +/- 51 to 56 +/- 17%. Exposure to benzamil doubled the beta-rbENaC protein level to 281 +/- 68% in control cells but had no significant effect on aldosterone-stimulated beta-rbENaC levels (282 +/- 68%). In conclusion, stimulation of apical Na+ entry suppresses the aldosterone-induced increase in transepithelial Na+ transport. This negative-feedback inhibition is reflected in a decrease in beta-rbENaC synthesis or in an increase in beta-rbENaC degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldosterone / pharmacology*
  • Amiloride / analogs & derivatives
  • Amiloride / pharmacology
  • Animals
  • Biological Transport / drug effects
  • Biological Transport / physiology
  • Cell Polarity / physiology
  • Cells, Cultured
  • Epithelial Sodium Channels
  • Extracellular Space / metabolism
  • Feedback / physiology
  • Kidney Tubules, Collecting / cytology
  • Kidney Tubules, Collecting / metabolism*
  • Rabbits
  • Sodium / metabolism*
  • Sodium Channels / biosynthesis*
  • Sulfur Radioisotopes

Substances

  • Epithelial Sodium Channels
  • Sodium Channels
  • Sulfur Radioisotopes
  • benzamil
  • Aldosterone
  • Amiloride
  • Sodium