Effects of amlodipine on native cardiac Na+ channels and cloned alpha-subunits of cardiac Na+ channels

Arzneimittelforschung. 1999 May;49(5):394-7. doi: 10.1055/s-0031-1300433.

Abstract

The inhibitory effects of amlodipine besilate (CAS 11470-99-6) on the native Na+ current (INa) and cloned human cardiac Na+ channel alpha subunit (hH1) were studied by whole cell patch clamp techniques. Amlodipine produced tonic block of INa in a concentration- and holding potential (HP)-dependent manner with hyperpolarization of H infinity. Amlodipine produced phasic blockade of INa, which was dependent on HP and pulse duration. Amlodipine produced tonic blockade of hH1 in a concentration-dependent manner with 1 : 1 stoichiometry, and phasic blockade of hH1 which was dependent on the pulse duration. Amlodipine blocked INa in a voltage- and frequency-dependent manner via affinity to the resting as well as inactivated conformations of the alpha subunit.

MeSH terms

  • Algorithms
  • Amlodipine / pharmacology*
  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Cloning, Molecular
  • Epithelial Sodium Channels
  • Guinea Pigs
  • Heart / drug effects*
  • Humans
  • In Vitro Techniques
  • Kinetics
  • Myocardium / cytology
  • Myocardium / metabolism
  • Patch-Clamp Techniques
  • Protein Conformation
  • Sodium Channel Blockers*
  • Sodium Channels / metabolism
  • Tetrodotoxin / pharmacology

Substances

  • Calcium Channel Blockers
  • Epithelial Sodium Channels
  • Sodium Channel Blockers
  • Sodium Channels
  • Amlodipine
  • Tetrodotoxin