The role of voltage-gated Ca2+ channels in anoxic injury of spinal cord white matter

Brain Res. 1999 Jan 30;817(1-2):84-92. doi: 10.1016/s0006-8993(98)01214-1.

Abstract

Dorsal column axons of the rat spinal cord are partially protected from anoxic injury following blockade of voltage-sensitive Na+ channels and the Na+/--Ca2+ exchanger. To examine the potential contribution of voltage-gated Ca2+ channels to anoxic injury of spinal cord axons, we studied axonal conduction in rat dorsal columns in vitro following a 60-min period of anoxia. Glass microelectrodes were used to record field potentials from the dorsal columns following distal local surface stimulation. Perfusion solutions containing blockers of voltage-gated Ca2+ channels were introduced 60 min prior to onset of anoxia and continued until 10 min after reoxygenation. Pharmacological blocking agents which are relatively selective for L- (verapamil, diltiazem, nifedipine) and N- (omega-conotoxin GVIA) type calcium channels were significantly protective against anoxia-induced loss of conduction, as was non-specific block using divalent cations. Other Ca2+ channel blockers (neomycin and omega-conotoxin MVIIC) that affect multiple Ca2+ channel types were also neuroprotective. Ni2+, which preferentially blocks R-type Ca2+ channels more than T-type channels, was also protective in a dose-dependent manner. These data suggest that the influx of Ca2+, through L-, N- and possibly R-type voltage-gated Ca2+ channels, participates in the pathophysiology of the Ca2+-mediated injury of spinal cord axons that is triggered by anoxia.

MeSH terms

  • Animals
  • Axons / pathology*
  • Calcium Channel Blockers / pharmacology
  • Calcium Channels / drug effects
  • Calcium Channels / physiology*
  • Cations, Divalent / pharmacology
  • Electric Stimulation
  • Female
  • Hypoxia / pathology
  • Hypoxia / physiopathology*
  • Ion Channel Gating*
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Peptides / pharmacology
  • Rats
  • Rats, Wistar
  • Sodium-Calcium Exchanger / physiology
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Spinal Cord / drug effects
  • Spinal Cord / pathology*
  • omega-Conotoxin GVIA
  • omega-Conotoxins*

Substances

  • Calcium Channel Blockers
  • Calcium Channels
  • Cations, Divalent
  • Peptides
  • Sodium-Calcium Exchanger
  • omega-Conotoxins
  • omega-conotoxin-MVIIC
  • omega-Conotoxin GVIA
  • Sodium-Potassium-Exchanging ATPase