Amiloride inhibits hydrogen peroxide-induced Ca2+ responses in human CNS pericytes

Microvasc Res. 2009 May;77(3):327-34. doi: 10.1016/j.mvr.2008.12.001. Epub 2008 Dec 25.

Abstract

The aims of the present study were to investigate the mechanisms of Ca(2+) signaling caused by hydrogen peroxide in CNS pericytes. In cultured human brain microvascular pericytes, cytosolic Ca(2+) concentration was measured by means of fura-2 fluorescence. Reverse transcription and polymerase chain reaction was performed to examine the expression of mRNA. Knockdown of Na(+)/H(+) exchanger (NHE) was done by transfecting the cells with specific double-strand siRNAs for NHE. Externally applied hydrogen peroxide dose-dependently (100 microM-10 mM) increased cytosolic Ca(2+) in human CNS pericytes. Cytosolic Ca(2+) remained high after wash-out of hydrogen peroxide. However, the addition of dithiothreitol rapidly reversed cytosolic Ca(2+) to the resting level. The hydrogen peroxide-induced Ca(2+) increase was not inhibited by nicardipine, Gd(3+), La(3+), or omission of external Ca(2+). Neither thapsigargin nor carbonyl cyanide 4-trifluoromethoxyphenylhydrazone attenuated the hydrogen peroxide-induced Ca(2+) rise. Amiloride and its derivatives, benzamil and hexamethylene amiloride reversed the hydrogen peroxide-induced Ca(2+) increase. Human CNS pericytes expressed acid sensing ion channel (ASIC) 1a, Na(+)/Ca(2+) exchanger (NCX) 1, Na(+)/H(+) exchanger (NHE) 1, and NHE7. However, the removal of external Na(+), treatment with KB-R 7943 and mibefradil, or knockdown of NHE1 and NHE7 did not affect the hydrogen peroxide-induced Ca(2+) increase. Hydrogen peroxide releases Ca(2+) from intracellular Ca(2+) pool via an amiloride-sensitive protein, which is controlled by oxidation of thiol group in human CNS pericytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acid Sensing Ion Channels
  • Amiloride / analogs & derivatives
  • Amiloride / pharmacology*
  • Brain / blood supply
  • Calcium / metabolism
  • Calcium Signaling / drug effects*
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Cell Line
  • Cytosol / chemistry
  • Cytosol / metabolism
  • Dithiothreitol / pharmacology
  • Drug Antagonism
  • Gene Silencing
  • Humans
  • Hydrogen Peroxide / pharmacology*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Oxidants / pharmacology*
  • Pericytes / drug effects*
  • Pericytes / metabolism
  • Sodium Channel Blockers / pharmacology*
  • Sodium Channels / genetics
  • Sodium Channels / metabolism
  • Sodium-Calcium Exchanger / genetics
  • Sodium-Calcium Exchanger / metabolism
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers / genetics
  • Sodium-Hydrogen Exchangers / metabolism

Substances

  • Acid Sensing Ion Channels
  • Cation Transport Proteins
  • Nerve Tissue Proteins
  • Oxidants
  • SLC9A1 protein, human
  • SLC9A7 protein, human
  • Sodium Channel Blockers
  • Sodium Channels
  • Sodium-Calcium Exchanger
  • Sodium-Hydrogen Exchanger 1
  • Sodium-Hydrogen Exchangers
  • sodium-calcium exchanger 1
  • Amiloride
  • Hydrogen Peroxide
  • Calcium
  • Dithiothreitol