Source:http://linkedlifedata.com/resource/pubmed/id/11726243
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2001-11-29
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pubmed:abstractText |
The effectiveness of tetraethylammonium (TEA) and high-frequency stimulation (HFS) in inducing long-term synaptic modification is compared in CA1 and dentate gyrus (DG) in vitro. High-frequency stimulation induces long-term potentiation (LTP) at synapses of both perforant path-DG granule cell and Schaffer collateral-CA1 pyramidal cell pathways. By contrast, TEA (25 mM) induces long-term depression in DG while inducing LTP in CA1. The mechanisms underlying the differential effect of TEA in CA1 and DG were investigated. It was observed that T-type voltage-dependent calcium channel (VDCC) blocker, Ni2+ (50 microM), partially blocked TEA-induced LTP in CA1. A complete blockade of the TEA-induced LTP occurred when Ni2+ was applied together with the NMDA receptor antagonist, D-APV. The L-type VDCC blocker, nifidipine (20 microM), had no effect on CA1 TEA-induced LTP. In DG of the same slice, TEA actually induced long-term depression (LTD) instead of LTP, an effect that was blocked by D-APV. Neither T-type nor L-type VDCC blockade could prevent this LTD. When the calcium concentration in the perfusion medium was increased, TEA induced a weak LTP in DG that was blocked by Ni2+. During exposure to TEA, the magnitude of field EPSPs was increased in both CA1 and DG, but the increase was substantially greater in CA1. Tetraethylammonium application also was associated with a large, late EPSP component in CA1 that persisted even after severing the connections between CA3 and CA1. All of the TEA effects in CA1, however, were dramatically reduced by Ni2+. The results of this study indicate that TEA indirectly acts via both T-type VDCCs and NMDA receptors in CA1 and, as a consequence, induces LTP. By contrast, TEA indirectly acts via only NMDA receptors in DG and results in LTD. The results raise the possibility of a major synaptic difference in the density and/or distribution of T-type VDCCs and NMDA receptors in CA1 and DG of the rat hippocampus.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2-Amino-5-phosphonovalerate,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Nickel,
http://linkedlifedata.com/resource/pubmed/chemical/Nifedipine,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channel Blockers,
http://linkedlifedata.com/resource/pubmed/chemical/Tetraethylammonium,
http://linkedlifedata.com/resource/pubmed/chemical/nickel chloride
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pubmed:status |
MEDLINE
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pubmed:month |
Nov
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pubmed:issn |
1074-7427
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 2001 Elsevier Science.
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pubmed:issnType |
Print
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pubmed:volume |
76
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
375-87
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:11726243-2-Amino-5-phosphonovalerate,
pubmed-meshheading:11726243-Animals,
pubmed-meshheading:11726243-Calcium Channel Blockers,
pubmed-meshheading:11726243-Dentate Gyrus,
pubmed-meshheading:11726243-Electric Stimulation,
pubmed-meshheading:11726243-Excitatory Amino Acid Antagonists,
pubmed-meshheading:11726243-Hippocampus,
pubmed-meshheading:11726243-Long-Term Potentiation,
pubmed-meshheading:11726243-Male,
pubmed-meshheading:11726243-Nickel,
pubmed-meshheading:11726243-Nifedipine,
pubmed-meshheading:11726243-Potassium Channel Blockers,
pubmed-meshheading:11726243-Rats,
pubmed-meshheading:11726243-Rats, Sprague-Dawley,
pubmed-meshheading:11726243-Synaptic Transmission,
pubmed-meshheading:11726243-Tetraethylammonium
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pubmed:year |
2001
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pubmed:articleTitle |
Differential effect of TEA on long-term synaptic modification in hippocampal CA1 and dentate gyrus in vitro.
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pubmed:affiliation |
Department of Biomedical Engineering, University of Southern California, Los Angeles 90089, USA. dsong@usc.edu
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
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