Source:http://linkedlifedata.com/resource/pubmed/id/11074153
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-1-4
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pubmed:abstractText |
Substance P, which modulates synaptic excitability, can be induced by a variety of stimuli. We studied the expression of hippocampal substance P in rats in using lithium-pilocarpine model of status epilepticus during development. Status epilepticus resulted in an age-specific manner of substance P expression that was anatomically distinctive in hippocampal subfields. Maximal induction of substance P immunoreactivity was seen in the CA1 region of the two-week-old rats, and progressively decreased in the three-, four-week-old rats and adults. Meanwhile, the number of substance P-immunoreactive neurons in the CA3 region and dentate granule cell layer was minimal in the two-week-old animals, but approximated the adult level in the three- and four-week-old rats. No substance P-immunoreactive axon terminals were seen in the strata pyramidale and lucidum in the CA3 region of the two-week-old rats, but they were found to progressively increase in the three-, four-week-old rats and adults. To confirm substance P expression after status epilepticus, we studied the expression of preprotachykinin-A mRNA in the hippocampus of the three-week-old rats by in situ hybridization. Two hours following injection of lithium-pilocarpine, preprotachykinin-A mRNA dramatically increased in the granule cells, as well as in the CA3 and CA1 pyramidal cell layers of the hippocampus. To evaluate the relationship between behavioral seizures and substance P induction, we used the NMDA receptor antagonist MK-801. Injection of MK-801 completely blocked lithium-pilocarpine-induced behavioral seizures and SP induction in the two-week-old rats. These results indicate that seizure activity selectively evokes age-dependent and region-selective expression of substance P.
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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/Dizocilpine Maleate,
http://linkedlifedata.com/resource/pubmed/chemical/Lithium Chloride,
http://linkedlifedata.com/resource/pubmed/chemical/Pilocarpine,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, N-Methyl-D-Aspartate,
http://linkedlifedata.com/resource/pubmed/chemical/Substance P,
http://linkedlifedata.com/resource/pubmed/chemical/Tachykinins,
http://linkedlifedata.com/resource/pubmed/chemical/preprotachykinin
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pubmed:status |
MEDLINE
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pubmed:issn |
0306-4522
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
101
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
297-304
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pubmed:dateRevised |
2009-11-3
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pubmed:meshHeading |
pubmed-meshheading:11074153-Age Factors,
pubmed-meshheading:11074153-Animals,
pubmed-meshheading:11074153-Dizocilpine Maleate,
pubmed-meshheading:11074153-Female,
pubmed-meshheading:11074153-Hippocampus,
pubmed-meshheading:11074153-Lithium Chloride,
pubmed-meshheading:11074153-Male,
pubmed-meshheading:11074153-Neural Pathways,
pubmed-meshheading:11074153-Neurons,
pubmed-meshheading:11074153-Pilocarpine,
pubmed-meshheading:11074153-Protein Precursors,
pubmed-meshheading:11074153-Rats,
pubmed-meshheading:11074153-Rats, Wistar,
pubmed-meshheading:11074153-Receptors, N-Methyl-D-Aspartate,
pubmed-meshheading:11074153-Status Epilepticus,
pubmed-meshheading:11074153-Substance P,
pubmed-meshheading:11074153-Tachykinins
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pubmed:year |
2000
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pubmed:articleTitle |
Patterns of status epilepticus-induced substance P expression during development.
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pubmed:affiliation |
Epilepsy Research Laboratory, Veteran Administration Medical Center, Sepulveda, CA 91343, USA. htliu@ucla.edu
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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