Pharmacological modulation of intracellular Ca(2+) channels at the single-channel level

Mol Neurobiol. 2001 Aug-Dec;24(1-3):65-86. doi: 10.1385/MN:24:1-3:065.

Abstract

Synaptic signaling, memory formation, neuronal development, and neuronal pathology are strongly influenced by the properties of intracellular Ca2+ channels, ryanodine, and inositol 1, 4, 5 trisphosphate receptors. This review will focus on recently developed and discovered pharmacological tools to modulate these channel proteins at the single-channel level. It will allow the readers of Molecular Neurobiology to evaluate the current knowledge on the pharmacological modulation of intracellular Ca2+ channels and to direct future research efforts effectively using available experimental tools and concepts.

Publication types

  • Review

MeSH terms

  • Animals
  • Calcium Channels / drug effects
  • Calcium Channels / physiology*
  • Ethanol / pharmacology
  • Inositol 1,4,5-Trisphosphate Receptors
  • Intracellular Fluid / physiology
  • Neurons / physiology
  • Polyamines / pharmacology
  • Receptors, Cytoplasmic and Nuclear / drug effects
  • Receptors, Cytoplasmic and Nuclear / physiology
  • Ruthenium Red / pharmacology
  • Ryanodine Receptor Calcium Release Channel / drug effects
  • Ryanodine Receptor Calcium Release Channel / physiology
  • Signal Transduction
  • Sulfhydryl Reagents / pharmacology
  • Synapses / physiology*

Substances

  • Calcium Channels
  • Inositol 1,4,5-Trisphosphate Receptors
  • Polyamines
  • Receptors, Cytoplasmic and Nuclear
  • Ryanodine Receptor Calcium Release Channel
  • Sulfhydryl Reagents
  • Ruthenium Red
  • Ethanol