Effect of L-type calcium channel blockers on activity of newly formed synapses in mice

Bull Exp Biol Med. 2007 Feb;143(2):171-4. doi: 10.1007/s10517-007-0041-y.

Abstract

Verapamil (5 microM), nifedipine (10 microM), and ryanodine (10 microM) potentiated rhythmic activity of newly formed synapses, while apamin produced no effect on this potentiation. Ryanodine (1 microM) suppressed synaptic activity, and this effect can be prevented with nifedipine. It was hypothesized that in newly formed synapses Ca2+ entry through L-type channels triggers the release of stored Ca2+, which inhibits secretion of the neurotransmitter.

MeSH terms

  • Action Potentials / drug effects
  • Animals
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels, L-Type / physiology*
  • Electrophysiology
  • Mice
  • Motor Endplate / drug effects
  • Motor Endplate / physiology
  • Nifedipine / pharmacology
  • Ryanodine / pharmacology
  • Synapses / drug effects*
  • Synapses / physiology
  • Verapamil / pharmacology

Substances

  • Calcium Channel Blockers
  • Calcium Channels, L-Type
  • Ryanodine
  • Verapamil
  • Nifedipine