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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6329
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pubmed:dateCreated |
1991-8-5
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pubmed:databankReference | |
pubmed:abstractText |
Kainic acid is a potent neurotoxin for certain neurons. Its neurotoxicity is thought to be mediated by an excitatory amino-acid-gated ion channel (ionotropic receptor) possessing nanomolar affinity for kainate. Here we describe a new member of the rat excitatory amino-acid receptor gene family, KA-1, that has a 30% sequence similarity with the previously characterized alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid (AMPA) receptor subunits GluR-A to -D. The pharmacological profile of expressed recombinant KA-1 determined in binding experiments with [3H]kainate is different from that of the cloned AMPA receptors and similar to the mammalian high-affinity kainate receptor (kainate greater than quisqualate greater than glutamate much greater than AMPA) with a dissociation constant of about 5 nM for kainate. The selectively high expression of KA-1 messenger RNA in the CA3 region of the hippocampus closely corresponds to autoradiographically located high-affinity kainate binding sites. This correlation, as well as the particular in vivo pattern of neurodegeneration observed on kainate-induced neurotoxicity, suggests that KA-1 participates in receptors mediating the kainate sensitivity of neurons in the central nervous system.
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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/Kainic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Kainic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Neurotransmitter,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0028-0836
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
351
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
742-4
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1648176-Amino Acid Sequence,
pubmed-meshheading:1648176-Animals,
pubmed-meshheading:1648176-Base Sequence,
pubmed-meshheading:1648176-Binding, Competitive,
pubmed-meshheading:1648176-Brain,
pubmed-meshheading:1648176-Cell Line,
pubmed-meshheading:1648176-Cloning, Molecular,
pubmed-meshheading:1648176-Gene Expression,
pubmed-meshheading:1648176-Hippocampus,
pubmed-meshheading:1648176-Humans,
pubmed-meshheading:1648176-Kainic Acid,
pubmed-meshheading:1648176-Molecular Sequence Data,
pubmed-meshheading:1648176-RNA, Messenger,
pubmed-meshheading:1648176-Rats,
pubmed-meshheading:1648176-Receptors, Kainic Acid,
pubmed-meshheading:1648176-Receptors, Neurotransmitter,
pubmed-meshheading:1648176-Recombinant Proteins,
pubmed-meshheading:1648176-Sequence Homology, Nucleic Acid,
pubmed-meshheading:1648176-Tissue Distribution,
pubmed-meshheading:1648176-Transfection
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pubmed:year |
1991
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pubmed:articleTitle |
Cloning of a putative high-affinity kainate receptor expressed predominantly in hippocampal CA3 cells.
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pubmed:affiliation |
Laboratory of Molecular Neuroendocrinology, Centre for Molecular Biology, University of Heidelberg, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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