Determinants of voltage-dependent inactivation affect Mibefradil block of calcium channels

Neuropharmacology. 2000;39(1):1-10. doi: 10.1016/s0028-3908(99)00153-7.


The voltage gated calcium channel family is a major target for a range of therapeutic drugs. Mibefradil (Ro 40-5967) belongs to a new chemical class of these molecules which differs from other Ca2+ antagonists by its ability to potently block T-type Ca2+ channels. However, this molecule has also been shown to inhibit other Ca2+ channel subtypes. To further analyze the mechanism governing the Ca2+ channel-Mibefradil interaction, we examined the effect of Mibefradil on various recombinant Ca2+ channels expressed in mammalian cells from their cloned cDNAs, using Ca2+ as the permeant ion at physiological concentration. Expression of alpha1A, alpha1C, and alpha1E in tsA 201 cells resulted in Ca2+ currents with functional characteristics closely related to those of their native counterparts. Mibefradil blocked alpha1A and alpha1E with a Kd comparable to that reported for T-type channels, but had a lower affinity (approximately 30-fold) for alpha1C. For each channel, inhibition by Mibefradil was consistent with high-affinity binding to the inactivated state. Modulation of the voltage-dependent inactivation properties by the nature of the coexpressed beta subunit or the alpha1 splice variant altered block at the Mibefradil receptor site. Therefore, we conclude that the tissue and sub-cellular localization of calcium channel subunits as well as their specific associations are essential parameters to understand the in vivo effects of Mibefradil.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alternative Splicing
  • Animals
  • Calcium Channel Blockers / pharmacology*
  • Calcium Channels, L-Type / drug effects
  • Calcium Channels, L-Type / genetics
  • Calcium Channels, L-Type / physiology*
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / physiology
  • Genes, Reporter
  • Genetic Vectors
  • Macromolecular Substances
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mibefradil / pharmacology*
  • Oocytes
  • Recombinant Proteins / drug effects
  • Vertebrates
  • Xenopus laevis


  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Macromolecular Substances
  • Recombinant Proteins
  • Mibefradil