Chronic furosemide or hydrochlorothiazide administration increases H+-ATPase B1 subunit abundance in rat kidney

Am J Physiol Renal Physiol. 2007 Jun;292(6):F1701-9. doi: 10.1152/ajprenal.00270.2006. Epub 2007 Feb 20.

Abstract

Furosemide administration stimulates distal acidification. This has been attributed to the increased lumen-negative voltage in the distal nephron, but the aspect of regulatory mechanisms of H(+)-ATPase has not been clear. The purpose of this study is to investigate whether chronic administration of diuretics alters the expression of H(+)-ATPase and whether electrogenic Na(+) reabsorption is involved in this process. A 7-day infusion of furosemide or hydrochlorothiazide (HCTZ) lowered urine pH significantly. However, this effect of furosemide-induced distal acidification was not changed with amiloride-blocking electrogenic Na(+) reabsorption. On immunoblotting, a polyclonal antibody against the H(+)-ATPase B1 subunit recognized a specific approximately 56-kDa band in membrane fractions from the kidney. The protein abundance of H(+)-ATPase was significantly increased by furosemide and HCTZ infusion in both the cortex and outer medulla. Furosemide plus amiloride administration also increased the H(+)-ATPase protein abundance significantly. However, no definite subcellular redistribution of H(+)-ATPase was observed by furosemide +/- amiloride infusion with immunohistochemistry. Chronic furosemide +/- amiloride administration induced a translocation of pendrin to the apical membrane, while total protein abundance was not increased. The mRNA expression of H(+)-ATPase was not altered by furosemide +/- amiloride infusion. We conclude that chronic administration of diuretics enhances distal acidification by increasing the abundance of H(+)-ATPase irrespective of electrogenic Na(+) reabsorption. This upregulation of H(+)-ATPase in the intercalated cells may be the result of tubular hypertrophy by diuretics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Chloride-Bicarbonate Antiporters / metabolism
  • Diuretics / pharmacology*
  • Electrophoresis, Polyacrylamide Gel
  • Furosemide / pharmacology*
  • Hydrochlorothiazide / pharmacology*
  • Immunohistochemistry
  • Kidney / drug effects
  • Kidney / enzymology*
  • Kidney / pathology
  • Male
  • Proton-Translocating ATPases / biosynthesis*
  • Proton-Translocating ATPases / immunology
  • RNA / biosynthesis
  • Rats
  • Rats, Sprague-Dawley
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sodium / metabolism
  • Sulfate Transporters

Substances

  • Chloride-Bicarbonate Antiporters
  • Diuretics
  • Slc26A4 protein, rat
  • Sulfate Transporters
  • Hydrochlorothiazide
  • RNA
  • Furosemide
  • Sodium
  • Proton-Translocating ATPases