Repetitive hypoxic exposure of brain slices and electrophysiological responses as an experimental model for investigation of cerebroprotective measurements

Neurol Res. 1996 Aug;18(4):367-9. doi: 10.1080/01616412.1996.11740438.

Abstract

An in vitro hippocampal (CA 1 region, guinea pig) slice technique using repeated hypoxia was employed to model electrophysiological changes (DC-potentials and evoked potentials (EP) by stimulation of Schaffer-collaterals) occurring in the hypoxic CA1 pyramidal layer. A standardized neuronal response under repeated hypoxic conditions was observed in this model, consisting of disappearance of EP and a trend towards partially reversible, but progressive synaptic failure subsequent anoxic depolarisation (AD). Slices treated with the calcium antagonist nimodipine showed a prolongation of AD latency between the first and following hypoxias. So it seems possible to simulate hypoxic lesions of the brain tissue by using this in vitro slice model.

MeSH terms

  • Animals
  • Brain Ischemia / complications
  • Brain Ischemia / physiopathology
  • Calcium Channel Blockers / pharmacology
  • Calcium Channel Blockers / therapeutic use
  • Cell Hypoxia
  • Electric Stimulation
  • Energy Metabolism
  • Evoked Potentials / drug effects
  • Guinea Pigs
  • Hippocampus / drug effects
  • Hippocampus / physiopathology*
  • Hypoxia, Brain / drug therapy
  • Hypoxia, Brain / etiology
  • Hypoxia, Brain / physiopathology*
  • Membrane Potentials / drug effects
  • Neuroprotective Agents / pharmacology
  • Neuroprotective Agents / therapeutic use
  • Nimodipine / pharmacology
  • Nimodipine / therapeutic use
  • Pyramidal Cells / drug effects
  • Pyramidal Cells / physiology
  • Synaptic Transmission*

Substances

  • Calcium Channel Blockers
  • Neuroprotective Agents
  • Nimodipine