Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys

Bruce D Winegar1, M Bruce MacIver

  • 1Neuroscience Program, Department of Anesthesia, Stanford University School of Medicine, Stanford, CA 94305-5117, USA. bwinegar@stanford.edu

BMC Neuroscience
|January 18, 2006
PubMed
Abstract

Insights

Isoflurane depresses hippocampal synapses by reducing glutamate release, acting downstream from sodium channels. This anesthetic effect involves presynaptic mechanisms, distinct from axonal conduction block.

Area of Science:

  • Neuroscience
  • Anesthesiology
  • Synaptic Transmission

Background:

  • Anesthetic-induced central nervous system (CNS) depression is linked to reduced glutamate release.
  • Isoflurane's mechanism may involve blocking sodium (Na) channels.
  • Investigating isoflurane's precise action on glutamate release is crucial.

Purpose of the Study:

  • To examine the effects of isoflurane on glutamate-mediated transmission at hippocampal excitatory synapses.
  • To differentiate isoflurane's action from Na channel blockade and other mechanisms.
  • To elucidate the presynaptic versus postsynaptic site of action for isoflurane.

Main Methods:

  • Recording excitatory postsynaptic potentials (EPSPs) in CA1 neurons of rat hippocampal slices.
  • Stimulating Schaffer-collateral fibers.
  • Applying isoflurane, tetrodotoxin (TTX), CNQX, and varying extracellular Ca2+ concentrations and stimulus voltage.

Main Results:

  • Isoflurane (1 MAC) reduced EPSP amplitudes by ~60% and increased facilitation, suggesting a presynaptic action.
  • TTX and altered stimulus voltage caused EPSP depression without changing facilitation, indicating axonal conduction failure.
  • Low extracellular Ca2+ mimicked isoflurane's effect on facilitation, while isoflurane did not affect fiber volleys.
  • Isoflurane's EC50 for fiber volley depression was high (~2.8 mM), indicating resistance.

Conclusions:

  • Isoflurane depresses CA1 synapses at presynaptic sites downstream from Na channels.
  • Increased synaptic facilitation during isoflurane application supports a presynaptic mechanism.
  • Isoflurane's effects on hippocampal synapses differ from those in other brain regions regarding fiber volley depression.