Renal Na/H exchanger NHE-3 and Na-PO4 cotransporter NaPi-2 protein expression in glucocorticoid excess and deficient states

J Am Soc Nephrol. 1998 Sep;9(9):1560-7. doi: 10.1681/ASN.V991560.

Abstract

Administration of pharmacologic doses of glucocorticoid in vivo increases renal proximal tubule apical membrane Na/H exchange and decreases Na/PO4 cotransport activity (1). Current data suggest that the NHE-3 and NaPi-2 proteins mediate significant fractions of proximal tubule apical membrane Na/H exchange and Na/PO4 cotransport, respectively. This study examines whether glucocorticoid excess or deficiency affects NHE-3 and NaPi-2 protein abundance and the intrarenal distribution of these transporters. Protein abundance of NHE-3 and NaPi-2 in control rats was compared to rats rendered glucocorticoid-deficient by bilateral adrenalectomy, and to rats receiving pharmacologic doses of dexamethasone using immunoblots and immunohistochemistry. Adrenalectomy had modest effects on NHE-3 protein abundance, but dexamethasone administration to either adrenalectomized or sham-operated rats significantly increased NHE-3 protein abundance in both the proximal tubule and thick ascending limb, but not the thin descending limb. Adrenalectomy increased NaPi-2 protein abundance in the proximal tubule, whereas dexamethasone administration dramatically suppressed NaPi-2 protein on the apical membrane in both adrenalectomized and sham-operated animals. No significant reciprocal increase in subapical NaPi-2 staining was seen in the dexamethasone-treated rats. The present study shows that glucocorticoids regulate proximal tubule apical membrane Na/H exchange and NaPi cotransport by changes in protein abundance of NHE-3 and NaPi-2, respectively.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adaptor Protein Complex 3
  • Adaptor Protein Complex beta Subunits*
  • Adrenalectomy
  • Analysis of Variance
  • Animals
  • Biological Transport, Active / physiology
  • Carrier Proteins / metabolism*
  • Disease Models, Animal
  • Glucocorticoids / deficiency
  • Glucocorticoids / metabolism*
  • Immunoblotting
  • Immunohistochemistry
  • Kidney Cortex / metabolism*
  • Male
  • Nerve Tissue Proteins / metabolism*
  • Phosphoproteins / metabolism*
  • Rats
  • Rats, Sprague-Dawley
  • Sensitivity and Specificity
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers / metabolism*
  • Sodium-Phosphate Cotransporter Proteins
  • Symporters*

Substances

  • AP3B2 protein, human
  • Adaptor Protein Complex 3
  • Adaptor Protein Complex beta Subunits
  • Carrier Proteins
  • Glucocorticoids
  • Nerve Tissue Proteins
  • Phosphoproteins
  • SLC9A3 protein, human
  • Slc9a3 protein, rat
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers
  • Sodium-Phosphate Cotransporter Proteins
  • Symporters