Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices

<p>Abstract</p> <p>Background</p> <p>Anesthesia is produced by a depression of central nervous system function, however, the sites and mechanisms of action underlying this depression remain poorly defined. The present study compared and contrasted effects produced by fi...

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Main Authors: MacIver M Bruce, Himmel Allison M, Pittson Sky
Format: Article
Language:English
Published: BMC 2004-12-01
Series:BMC Neuroscience
Online Access:http://www.biomedcentral.com/1471-2202/5/52
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author MacIver M Bruce
Himmel Allison M
Pittson Sky
author_facet MacIver M Bruce
Himmel Allison M
Pittson Sky
author_sort MacIver M Bruce
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Anesthesia is produced by a depression of central nervous system function, however, the sites and mechanisms of action underlying this depression remain poorly defined. The present study compared and contrasted effects produced by five general anesthetics on synaptic circuitry in the CA1 region of hippocampal slices.</p> <p>Results</p> <p>At clinically relevant and equi-effective concentrations, presynaptic and postsynaptic anesthetic actions were evident at glutamate-mediated excitatory synapses and at GABA-mediated inhibitory synapses. In addition, depressant effects on membrane excitability were observed for CA1 neuron discharge in response to direct current depolarization. Combined actions at several of these sites contributed to CA1 circuit depression, but the relative degree of effect at each site was different for each anesthetic studied. For example, most of propofol's depressant effect (> 70 %) was reversed with a GABA antagonist, but only a minor portion of isoflurane's depression was reversed (< 20 %). Differences were also apparent on glutamate synapses-pentobarbital depressed transmission by > 50 %, but thiopental by only < 25 %.</p> <p>Conclusions</p> <p>These results, in as much as they may be relevant to anesthesia, indicate that general anesthetics act at several discrete sites, supporting a multi-site, agent specific theory for anesthetic actions. No single effect site (e.g. GABA synapses) or mechanism of action (e.g. depressed membrane excitability) could account for all of the effects produced for any anesthetic studied.</p>
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spelling doaj.art-79956992835346e78808ba83edee35172022-12-21T23:13:12ZengBMCBMC Neuroscience1471-22022004-12-01515210.1186/1471-2202-5-52Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slicesMacIver M BruceHimmel Allison MPittson Sky<p>Abstract</p> <p>Background</p> <p>Anesthesia is produced by a depression of central nervous system function, however, the sites and mechanisms of action underlying this depression remain poorly defined. The present study compared and contrasted effects produced by five general anesthetics on synaptic circuitry in the CA1 region of hippocampal slices.</p> <p>Results</p> <p>At clinically relevant and equi-effective concentrations, presynaptic and postsynaptic anesthetic actions were evident at glutamate-mediated excitatory synapses and at GABA-mediated inhibitory synapses. In addition, depressant effects on membrane excitability were observed for CA1 neuron discharge in response to direct current depolarization. Combined actions at several of these sites contributed to CA1 circuit depression, but the relative degree of effect at each site was different for each anesthetic studied. For example, most of propofol's depressant effect (> 70 %) was reversed with a GABA antagonist, but only a minor portion of isoflurane's depression was reversed (< 20 %). Differences were also apparent on glutamate synapses-pentobarbital depressed transmission by > 50 %, but thiopental by only < 25 %.</p> <p>Conclusions</p> <p>These results, in as much as they may be relevant to anesthesia, indicate that general anesthetics act at several discrete sites, supporting a multi-site, agent specific theory for anesthetic actions. No single effect site (e.g. GABA synapses) or mechanism of action (e.g. depressed membrane excitability) could account for all of the effects produced for any anesthetic studied.</p>http://www.biomedcentral.com/1471-2202/5/52
spellingShingle MacIver M Bruce
Himmel Allison M
Pittson Sky
Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
BMC Neuroscience
title Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
title_full Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
title_fullStr Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
title_full_unstemmed Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
title_short Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
title_sort multiple synaptic and membrane sites of anesthetic action in the ca1 region of rat hippocampal slices
url http://www.biomedcentral.com/1471-2202/5/52
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