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Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices
BACKGROUND: 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...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC543467/ https://www.ncbi.nlm.nih.gov/pubmed/15579203 http://dx.doi.org/10.1186/1471-2202-5-52 |
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author | Pittson, Sky Himmel, Allison M MacIver, M Bruce |
author_facet | Pittson, Sky Himmel, Allison M MacIver, M Bruce |
author_sort | Pittson, Sky |
collection | PubMed |
description | BACKGROUND: 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. RESULTS: 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 %. CONCLUSIONS: 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. |
format | Text |
id | pubmed-543467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5434672005-01-08 Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices Pittson, Sky Himmel, Allison M MacIver, M Bruce BMC Neurosci Research Article BACKGROUND: 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. RESULTS: 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 %. CONCLUSIONS: 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. BioMed Central 2004-12-03 /pmc/articles/PMC543467/ /pubmed/15579203 http://dx.doi.org/10.1186/1471-2202-5-52 Text en Copyright © 2004 Pittson et al; licensee BioMed Central Ltd. |
spellingShingle | Research Article Pittson, Sky Himmel, Allison M MacIver, M Bruce Multiple synaptic and membrane sites of anesthetic action in the CA1 region of rat hippocampal slices |
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 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC543467/ https://www.ncbi.nlm.nih.gov/pubmed/15579203 http://dx.doi.org/10.1186/1471-2202-5-52 |
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