Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys
<p>Abstract</p> <p>Background</p> <p>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 questi...
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doaj-dfaaccb36b5849d18736c620e9edf5ce2020-11-25T01:03:06ZengBMCBMC Neuroscience1471-22022006-01-0171510.1186/1471-2202-7-5Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleysMacIver M BruceWinegar Bruce D<p>Abstract</p> <p>Background</p> <p>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 Ca<sup>2+</sup>, 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.</p> <p>Results</p> <p>Isoflurane (350 μM; 1 MAC) reversibly depressed EPSP amplitudes by ~60% while facilitation increased ~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 μM) depressed EPSP amplitudes with no change in facilitation. However, EPSP depression by low external Ca<sup>2+ </sup>(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 Ca<sup>2+ </sup>(4 mM) that also decreased facilitation. Isoflurane or low Ca<sup>2+ </sup>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 μM (1 MAC) isoflurane as well. The EC<sub>50 </sub>for isoflurane depression of FVs was ~2.8 mM (12 vol. %; 8 MAC).</p> <p>Conclusion</p> <p>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.</p> http://www.biomedcentral.com/1471-2202/7/5 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
MacIver M Bruce Winegar Bruce D |
spellingShingle |
MacIver M Bruce Winegar Bruce D Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys BMC Neuroscience |
author_facet |
MacIver M Bruce Winegar Bruce D |
author_sort |
MacIver M Bruce |
title |
Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys |
title_short |
Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys |
title_full |
Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys |
title_fullStr |
Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys |
title_full_unstemmed |
Isoflurane depresses hippocampal CA1 glutamate nerve terminals without inhibiting fiber volleys |
title_sort |
isoflurane depresses hippocampal ca1 glutamate nerve terminals without inhibiting fiber volleys |
publisher |
BMC |
series |
BMC Neuroscience |
issn |
1471-2202 |
publishDate |
2006-01-01 |
description |
<p>Abstract</p> <p>Background</p> <p>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 Ca<sup>2+</sup>, 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.</p> <p>Results</p> <p>Isoflurane (350 μM; 1 MAC) reversibly depressed EPSP amplitudes by ~60% while facilitation increased ~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 μM) depressed EPSP amplitudes with no change in facilitation. However, EPSP depression by low external Ca<sup>2+ </sup>(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 Ca<sup>2+ </sup>(4 mM) that also decreased facilitation. Isoflurane or low Ca<sup>2+ </sup>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 μM (1 MAC) isoflurane as well. The EC<sub>50 </sub>for isoflurane depression of FVs was ~2.8 mM (12 vol. %; 8 MAC).</p> <p>Conclusion</p> <p>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.</p> |
url |
http://www.biomedcentral.com/1471-2202/7/5 |
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