Source:http://linkedlifedata.com/resource/pubmed/id/14659520
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2003-12-8
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pubmed:abstractText |
In superficial layers of the lumbar spinal dorsal horn, N-methyl-D-aspartate-dependent long-term potentiation (LTP) of C fibre-evoked field potentials, a synaptic model of central sensitisation and hyperalgesia, ensues the application of electrical high-frequency, high-intensity conditioning stimulation to the sciatic nerve. In order to investigate the putative involvement of the G protein-coupled metabotropic glutamate receptors (mGluRs) in the induction of this form of LTP, we applied a series of mGluR antagonists exhibiting distinct group-specific activity profiles to the spinal lumbar enlargement, prior to conditioning stimulation. The group I (mGluR1/5) and group II (mGluR2/3) mGluR antagonist (S)-alpha-methyl-4-carboxyphenylglycine or the selective mGluR1/5 antagonist (S)-4-carboxyphenylglycine consistently impaired the development of spinal LTP. However, potentiation occurred in the presence of the inactive enantiomer (R)-alpha-methyl-4-carboxyphenylglycine. LTP proved insensitive to the selective mGluR2/3 antagonists (2S)-alpha-ethylglutamic acid and LY341495, either spinally or intravenously delivered. LTP could also be induced in the presence of the selective group III (mGluR4/mGluR6-mGluR8) mGluR antagonist (RS)-alpha-methylserine-O-phosphate. However, none of the mGluR-active compounds alone noticeably altered the amplitudes of C fibre-evoked field potentials in the absence of conditioning stimulation. These findings suggest that the induction of LTP of C fibre-evoked field potentials in the spinal dorsal horn by high-frequency, high-intensity stimulation of afferent C fibres requires a group-specific mGluR recruitment, activation of mGluR1/5 but not that of mGluR4/6-8 and mGluR2/3 being a requisite step.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Excitatory Amino Acid Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Metabotropic Glutamate,
http://linkedlifedata.com/resource/pubmed/chemical/metabotropic glutamate receptor 2,
http://linkedlifedata.com/resource/pubmed/chemical/metabotropic glutamate receptor 3,
http://linkedlifedata.com/resource/pubmed/chemical/metabotropic glutamate receptor...
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0304-3959
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
106
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
373-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14659520-Action Potentials,
pubmed-meshheading:14659520-Animals,
pubmed-meshheading:14659520-Electric Stimulation,
pubmed-meshheading:14659520-Excitatory Amino Acid Antagonists,
pubmed-meshheading:14659520-Long-Term Potentiation,
pubmed-meshheading:14659520-Male,
pubmed-meshheading:14659520-Nerve Fibers, Unmyelinated,
pubmed-meshheading:14659520-Rats,
pubmed-meshheading:14659520-Rats, Sprague-Dawley,
pubmed-meshheading:14659520-Receptors, Metabotropic Glutamate,
pubmed-meshheading:14659520-Spinal Cord
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pubmed:year |
2003
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pubmed:articleTitle |
Induction of long-term potentiation of C fibre-evoked spinal field potentials requires recruitment of group I, but not group II/III metabotropic glutamate receptors.
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pubmed:affiliation |
School of Medicine and Dentistry, The University of the Basque Country, Sarriena s/n 48940, Leioa, Spain.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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