Vinpocetine is as potent as phenytoin to block voltage-gated Na+ channels in rat cortical neurons

Eur J Pharmacol. 1995 Feb 6;273(3):303-6. doi: 10.1016/0014-2999(94)00755-v.

Abstract

The effects of vinpocetine and phenytoin on voltage-gated Na+ channels were examined on cultured cerebrocortical neurones of the rat using a conventional whole-cell patch-clamp method. Vinpocetine and phenytoin decreased Na+ currents in a concentration-dependent manner, with IC50 values of 44.2 +/- 14.6 and 50.5 +/- 17.4 microM, respectively. Both compounds shifted the voltage dependence of the steady-state inactivation of the channel in the hyperpolarising direction. This pronounced Na+ channel blocking activity may contribute to the neuroprotective and anticonvulsant effects of vinpocetine.

MeSH terms

  • Animals
  • Anticonvulsants / pharmacology*
  • Cells, Cultured
  • Cerebral Cortex / cytology
  • Cerebral Cortex / drug effects
  • Cerebral Cortex / metabolism*
  • Electrophysiology
  • Ion Channel Gating / drug effects*
  • Neurons / drug effects
  • Neurons / metabolism*
  • Patch-Clamp Techniques
  • Phenytoin / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Sodium Channels / drug effects*
  • Vinca Alkaloids / pharmacology*

Substances

  • Anticonvulsants
  • Sodium Channels
  • Vinca Alkaloids
  • vinpocetine
  • Phenytoin