Source:http://linkedlifedata.com/resource/pubmed/id/17021182
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rdf:type | |
lifeskim:mentions |
umls-concept:C0011570,
umls-concept:C0030685,
umls-concept:C0039062,
umls-concept:C0220839,
umls-concept:C0282114,
umls-concept:C0301630,
umls-concept:C0332281,
umls-concept:C0337051,
umls-concept:C0391871,
umls-concept:C0441843,
umls-concept:C0443252,
umls-concept:C0680255,
umls-concept:C1283071,
umls-concept:C1509144,
umls-concept:C1622418,
umls-concept:C1637379,
umls-concept:C1963578
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pubmed:issue |
40
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pubmed:dateCreated |
2006-10-5
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pubmed:abstractText |
Postsynaptic alterations have been suggested to account for NMDA receptor (NMDAR)-dependent long-term depression (LTD) and long-term potentiation of synaptic strength, although there is substantial evidence supporting changes in presynaptic release. Direct chemical activation of either NMDA or group I metabotropic glutamate receptor (mGluR1) elicits LTD of similar magnitudes, but it is unknown whether they share common expression mechanisms. Using dual-photon laser-scanning microscopy of FM1-43 [N-(3-triethylammoniumpropyl)-4-(4-(dibutylamino)styryl)pyridinium dibromide] to directly visualize presynaptic vesicular release from the rapidly recycling vesicle pool (RRP) at Schaffer collateral terminals in field CA1 of rat hippocampal slices, we found that a persistent reduction in vesicular release from the RRP is induced by NMDA-LTD but not by mGluR1-LTD. Variance-mean analyses of Schaffer collateral release probability (P(r)) at varying extracellular calcium concentrations confirmed that NMDA-LTD was associated with reduced P(r), whereas mGluR1-LTD was not. Pharmacological isolation of NMDAR-dependent and mGluR-dependent forms of stimulus-evoked LTD revealed that both are composed of a combination of presynaptic and postsynaptic alterations. However, when group I mGluR-dependent LTD was isolated by combining an NMDAR blocker with a group II mGluR antagonist, this form of LTD was purely postsynaptic. The nitric oxide synthase inhibitor N omega-nitro-L-arginine blocked the induction of NMDA-LTD but did not alter mGluR-LTD, consistent with a selective role for nitric oxide as a retrograde messenger mediating NMDA-LTD. These data demonstrate that single synapses can express multiple forms of LTD with different sites of expression, that NMDA-LTD is a combination of presynaptic and postsynaptic alterations, but that group I mGluR-LTD appears to be expressed entirely postsynaptically.
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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/N-Methylaspartate,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Metabotropic Glutamate,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, N-Methyl-D-Aspartate,
http://linkedlifedata.com/resource/pubmed/chemical/metabotropic glutamate receptor...
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1529-2401
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
4
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pubmed:volume |
26
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
10270-80
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:17021182-Animals,
pubmed-meshheading:17021182-Long-Term Potentiation,
pubmed-meshheading:17021182-N-Methylaspartate,
pubmed-meshheading:17021182-Presynaptic Terminals,
pubmed-meshheading:17021182-Rats,
pubmed-meshheading:17021182-Rats, Sprague-Dawley,
pubmed-meshheading:17021182-Receptors, Metabotropic Glutamate,
pubmed-meshheading:17021182-Receptors, N-Methyl-D-Aspartate,
pubmed-meshheading:17021182-Synapses,
pubmed-meshheading:17021182-Synaptic Transmission
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pubmed:year |
2006
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pubmed:articleTitle |
NMDA-dependent, but not group I metabotropic glutamate receptor-dependent, long-term depression at Schaffer collateral-CA1 synapses is associated with long-term reduction of release from the rapidly recycling presynaptic vesicle pool.
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pubmed:affiliation |
Department of Cell Biology and Anatomy, New York Medical College, Valhalla, New York 10595, USA.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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