Control of descending vasa recta pericyte membrane potential by angiotensin II

Am J Physiol Renal Physiol. 2002 Jun;282(6):F1064-74. doi: 10.1152/ajprenal.00306.2001.

Abstract

Using nystatin perforated-patch whole cell recording, we investigated the role of Cl(-) conductance in the modulation of outer medullary descending vasa recta (OMDVR) pericyte membrane potential (Psi m) by ANG II. ANG II (10(-11) to 10(-7) M) consistently depolarized OMDVR and induced Psi m oscillations at lower concentrations. The Cl(-) channel blockers anthracene-9-decarboxylate (1 mM) and niflumic acid (10 microM) hyperpolarized resting pericytes and repolarized ANG II-treated pericytes. In voltage-clamp experiments, ANG II-treated pericytes exhibited slowly activating currents that were nearly eliminated by treatment with niflumic acid (10 microM) or removal of extracellular Ca(2+). Those currents reversed at -31 and -10 mV when extracellular Cl(-) concentration was 152 and 34 mM, respectively. In pericytes held at -70 mV, oscillating inward currents were sometimes observed; the reversal potential also shifted with extracellular Cl(-) concentration. We conclude that ANG II activates a Ca(2+)-dependent Cl(-) conductance in OMDVR pericytes to induce membrane depolarization and Psi m oscillations.

Publication types

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

MeSH terms

  • Angiotensin II / pharmacology
  • Angiotensin II / physiology*
  • Animals
  • Biological Clocks / physiology
  • Chloride Channels / antagonists & inhibitors
  • Dose-Response Relationship, Drug
  • In Vitro Techniques
  • Kidney Medulla / blood supply*
  • Kidney Medulla / drug effects
  • Kidney Medulla / physiology
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Microcirculation / cytology
  • Microcirculation / drug effects
  • Microcirculation / physiology*
  • Niflumic Acid / pharmacology
  • Patch-Clamp Techniques
  • Pericytes / cytology
  • Pericytes / drug effects
  • Pericytes / physiology*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Chloride Channels
  • Angiotensin II
  • Niflumic Acid