Role of 20-HETE in mediating the effect of dietary K intake on the apical K channels in the mTAL

Am J Physiol Renal Physiol. 2001 Feb;280(2):F223-30. doi: 10.1152/ajprenal.2001.280.2.F223.

Abstract

We have used the patch-clamp technique to study the effect of dietary K intake on the apical K channels in the medullary thick ascending limb (mTAL) of rat kidneys. The channel activity, defined by the number of channels in a patch and the open probability (NPo), of the 30- and 70-pS K channels, was 0.18 and 0.11, respectively, in the mTAL from rats on a K-deficient diet. In contrast, NPo of the 30- and 70-pS K channels increased to 0.60 and 0.80, respectively, in the tubules from animals on a high-K diet. The concentration of 20-hydroxyeicosatetraenoic acid (20-HETE) measured with gas chromatography-mass spectrometry was 0.8 pg/microg protein in the mTAL from rats on a high-K diet and increased significantly to 4.6 pg/microg protein in the tubules from rats on a K-deficient diet. Addition of N-methylsulfonyl-12,12-dibromododec-11-enamide (DDMS) or 17-octadecynoic acid (17-ODYA), agents that inhibit the formation of 20-HETE, had no significant effect on the activity of the 30-pS K channels. However, DDMS/17-ODYA significantly increased the activity of the apical 70-pS K channel from 0.11 to 0.91 in the mTAL from rats on a K-deficient diet. In contrast, inhibition of the cytochrome P-450 metabolism of arachidonic acid increased NPo from 0.64 to 0.81 in the tubules from animals on a high-K diet. Furthermore, the sensitivity of the 70-pS K channel to 20-HETE was the same between rats on a high-K diet and on a K-deficient diet. Finally, the pretreatment of the tubules with DDMS increased NPo of the 70-pS K channels in the mTAL from rats on a K-deficient diet to 0.76. We conclude that an increase in 20-HETE production is involved in reducing the activity of the apical 70-pS K channels in the mTAL from rats on a K-deficient diet.

Publication types

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

MeSH terms

  • Amides / pharmacology
  • Animals
  • Enzyme Inhibitors / pharmacology
  • Hydroxyeicosatetraenoic Acids / pharmacology*
  • Hydroxyeicosatetraenoic Acids / physiology
  • Kidney Tubules / drug effects*
  • Kidney Tubules / physiology
  • Potassium Channels / drug effects*
  • Potassium Channels / physiology
  • Potassium, Dietary / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Sulfones / pharmacology

Substances

  • Amides
  • Enzyme Inhibitors
  • Hydroxyeicosatetraenoic Acids
  • Potassium Channels
  • Potassium, Dietary
  • Sulfones
  • 20-hydroxy-5,8,11,14-eicosatetraenoic acid
  • DDMS