Subtotal nephrectomy alters tubular function: effect of phosphorus restriction

Kidney Int. 1997 Dec;52(6):1550-60. doi: 10.1038/ki.1997.485.

Abstract

Few studies have examined tubular function after subtotal nephrectomy (Nx) and conservative treatments. The effects of 70% and 80% Nx (associated with dietary phosphate restriction in the latter case) on the apical brush border membrane (BBM) enzymes 5'-nucleotidase, gamma glutamyl-transferase and alkaline-phosphatase, and one BBM Na-phosphate cotransporter (NaPi-2) were studied in rats after a six week period. Changes in activity and mRNA abundance of the BBM enzymes and in NaPi-2 protein and mRNA abundance were compared with changes in the distal markers of Na,K-ATPase activity and epidermal growth factor (EGF) production. The activity, but not the mRNA of BBM enzymes, was moderately reduced by the 70% Nx. Both the mRNA and activity of gamma glutamyl-transferase and alkaline-phosphatase were decreased in the 80% Nx, and the NaPi-2 mRNA, protein and Na,K-ATPase activities were also reduced. These effects (except for 5'nucleotidase and Na,K-ATPase) were partly reversed by phosphate restriction. Overproduction of EGF occurred after the 70% Nx, was blunted in the 80% Nx, and then partially restored by phosphate restriction. Aggravation of tubular alteration was associated with enhanced renal hyperplasia (increased DNA mass), reduced GFR and hyperphosphatemia, and high PTH levels, but reduced cAMP excretion. Improvement following phosphate restriction was associated with reduced hyperplasia and lowering of phosphatemia and PTH levels. These data demonstrate that Nx selectively affected BBM function through transcriptional changes that were partially reversed by phosphate restriction. Regulatory factors involved in these changes may include intracellular phosphate content and growth factors, but not the PTH effects that are impaired in chronic renal failure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 5'-Nucleotidase / genetics
  • 5'-Nucleotidase / metabolism
  • Animals
  • Calcium / blood
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism
  • Cholecalciferol / blood
  • Epidermal Growth Factor / biosynthesis
  • Epidermal Growth Factor / metabolism
  • Gene Expression Regulation, Enzymologic / drug effects
  • Kidney Function Tests
  • Kidney Tubules / physiology*
  • Kidney Tubules / surgery*
  • Male
  • Membrane Proteins / metabolism
  • Microvilli / chemistry
  • Microvilli / drug effects
  • Microvilli / enzymology
  • Nephrectomy*
  • Organ Size
  • Organ Specificity
  • Parathyroid Hormone / blood
  • Phosphates / blood
  • Phosphates / urine
  • Phosphorus, Dietary / pharmacology*
  • RNA, Messenger / analysis
  • Rats
  • Rats, Sprague-Dawley
  • Sodium-Phosphate Cotransporter Proteins
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Symporters*
  • gamma-Glutamyltransferase / genetics
  • gamma-Glutamyltransferase / metabolism

Substances

  • Carrier Proteins
  • Membrane Proteins
  • Parathyroid Hormone
  • Phosphates
  • Phosphorus, Dietary
  • RNA, Messenger
  • Sodium-Phosphate Cotransporter Proteins
  • Symporters
  • Cholecalciferol
  • Epidermal Growth Factor
  • gamma-Glutamyltransferase
  • 5'-Nucleotidase
  • Sodium-Potassium-Exchanging ATPase
  • sodium phosphate
  • Calcium