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Whole-cell Patch-clamp Recordings from Morphologically- and Neurochemically-identified Hippocampal Interneurons
Published on: September 30, 2014
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
Background:
Anesthetic-induced CNS depression is thought to involve reduction of glutamate release from nerve terminals. Recent studies suggest that isoflurane reduces glutamate release by block of Na channels. To further investigate this question we examined the actions of isoflurane, TTX, extracellular Ca2+, CNQX and stimulus voltage (stim) on glutamate-mediated transmission at hippocampal excitatory synapses. EPSPs were recorded from CA1 neurons in rat hippocampal brain slices in response to Schaffer-collateral fiber stimulation.
Results:
Isoflurane (350 microM; 1 MAC) reversibly depressed EPSP amplitudes by ~60% while facilitation increased approximately 20%. Consistent with previous studies, these results indicate a presynaptic site of action that involves reduced excitation-release coupling. EPSPs were depressed to comparable levels by TTX (60 nM) or lowered stim, but facilitation was not changed, indicating a simple failure of axonal conduction. Similarly, partial antagonism of postsynaptic glutamate receptors with CNQX (10 microM) depressed EPSP amplitudes with no change in facilitation. However, EPSP depression by low external Ca2+ (0.8 mM) was accompanied by an increase in facilitation comparable to isoflurane. Isoflurane depression of EPSP amplitudes could also be partly reversed by high external Ca2+ (4 mM) that also decreased facilitation. Isoflurane or low Ca2+ markedly reduced the slopes of fiber volley (FV)-EPSP input-output curves, consistent with little or no effect on FVs. By contrast, TTX didn't alter the FV-EPSP curve slope, indicating that EPSP depression resulted from FV depression. FVs were remarkably resistant to isoflurane. Somatic spike currents were unaffected by 350 microM (1 MAC) isoflurane as well. The EC50 for isoflurane depression of FVs was approximately 2.8 mM (12 vol. %; 8 MAC).
Conclusion:
Isoflurane appears to depress CA1 synapses at presynaptic sites downstream from Na channels, as evident by the increased facilitation that accompanies EPSP depression. Fiber volleys did not exhibit depression by isoflurane, as has been reported for other brain regions.
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.
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