Elevated BSC-1 and ROMK expression in Dahl salt-sensitive rat kidneys

Hypertension. 2004 Apr;43(4):860-5. doi: 10.1161/01.HYP.0000120123.44945.47. Epub 2004 Feb 16.

Abstract

This study compared the expression of enzymes and transport and channel proteins involved in the regulation of sodium reabsorption in the kidney of Dahl salt-sensitive (DS) and salt-resistant Brown-Norway (BN) and consomic rats (SS.BN13), in which chromosome 13 from the BN rat has been introgressed into the DS genetic background. The expression of the Na+/K+/2Cl- (BSC-1) cotransporter, Na+/H+ exchanger (NHE3), and Na+-K+-ATPase proteins were similar in the renal cortex of DS, BN, and SS.BN13 rats fed either a low-salt (0.1% NaCl) or a high-salt (8% NaCl) diet. The expression of the BSC-1 and the renal outer medullary K+ channel (ROMK) were higher, whereas the expression of the cytochrome P4504A proteins responsible for the formation of 20-hydroxyeicosatetraenoic (20-HETE) was lower in the outer medulla of the kidney of DS than in BN or SS.BN13 rats fed either a low-salt or a high-salt diet. In addition, the renal formation and excretion of 20-HETE was lower in DS than in BN and SS.BN13 rats. These results suggest that overexpression of ROMK and BSC-1 in the thick ascending limb combined with a deficiency in renal formation of 20-HETE may predispose Dahl S rats fed a high-salt diet to Na+ retention and hypertension.

Publication types

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

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Arachidonic Acid / metabolism
  • Blood Pressure / genetics
  • Blood Pressure / physiology*
  • Chromosomes / genetics
  • Cytochrome P-450 CYP4A / biosynthesis
  • Cytochrome P-450 CYP4A / genetics
  • Diet, Sodium-Restricted
  • Genetic Predisposition to Disease
  • Hydroxyeicosatetraenoic Acids / metabolism
  • Hypertension / genetics*
  • Hypertension / metabolism
  • Hypertension / physiopathology
  • Ion Transport
  • Kidney Cortex / metabolism*
  • Kidney Medulla / metabolism
  • Loop of Henle / metabolism*
  • Male
  • Natriuresis / genetics
  • Natriuresis / physiology*
  • Potassium Channels / biosynthesis
  • Potassium Channels / genetics
  • Potassium Channels / physiology*
  • Potassium Channels, Inwardly Rectifying*
  • Rats
  • Rats, Inbred BN
  • Rats, Inbred Dahl
  • Sodium / metabolism*
  • Sodium Chloride, Dietary / administration & dosage
  • Sodium Chloride, Dietary / pharmacokinetics
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers / biosynthesis
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Potassium-Chloride Symporters / biosynthesis
  • Sodium-Potassium-Chloride Symporters / genetics
  • Sodium-Potassium-Chloride Symporters / physiology*
  • Sodium-Potassium-Exchanging ATPase / biosynthesis
  • Sodium-Potassium-Exchanging ATPase / genetics
  • Solute Carrier Family 12, Member 1

Substances

  • Hydroxyeicosatetraenoic Acids
  • Kcnj1 protein, rat
  • Potassium Channels
  • Potassium Channels, Inwardly Rectifying
  • Slc12a1 protein, rat
  • Slc9a3 protein, rat
  • Sodium Chloride, Dietary
  • Sodium-Hydrogen Exchanger 3
  • Sodium-Hydrogen Exchangers
  • Sodium-Potassium-Chloride Symporters
  • Solute Carrier Family 12, Member 1
  • Arachidonic Acid
  • 20-hydroxy-5,8,11,14-eicosatetraenoic acid
  • Sodium
  • Cytochrome P-450 CYP4A
  • Sodium-Potassium-Exchanging ATPase