Source:http://linkedlifedata.com/resource/pubmed/id/11595342
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2001-10-11
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pubmed:abstractText |
Kainate-type receptor channels (GluR5-7, KA1,2) belong to the family of ionotropic glutamate receptor channels. In the present study we tested the interaction of two different drugs with GluR6 channels using outside-out patches from HEK cells transiently transfected with cDNA of GluR6 channels. Glutamate and the respective drugs were delivered by a system for ultrafast solution exchange. Application of a saturating concentration of 3 mM glutamate resulted in fast current transients with desensitization time constants between 3 and 10 ms. Addition of pentobarbital (>or=1 mM) to the 3 mM glutamate containing test-solution resulted in a significant decrease of the time constant of current decay without affecting the peak current amplitude. Brilliant green (>or=1 mM) had the opposite effect and led to an increase of the time constant of current decay after application of 3 mM glutamate. The pharmacological effects of both drugs were completely reversible. Additionally, a significant increase of the peak current amplitude and the time constant of deactivation in presence of brilliant green was observed. Summarizing our results, we could identify a further substance, brilliant green, interacting with GluR6 kainate-type receptor channels.
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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/Coloring Agents,
http://linkedlifedata.com/resource/pubmed/chemical/GABA Modulators,
http://linkedlifedata.com/resource/pubmed/chemical/Gluk2 kainate receptor,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Pentobarbital,
http://linkedlifedata.com/resource/pubmed/chemical/Quaternary Ammonium Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Kainic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/brilliant green
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0304-3940
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
19
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pubmed:volume |
312
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
91-4
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pubmed:dateRevised |
2010-1-13
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pubmed:meshHeading |
pubmed-meshheading:11595342-Cells, Cultured,
pubmed-meshheading:11595342-Central Nervous System,
pubmed-meshheading:11595342-Coloring Agents,
pubmed-meshheading:11595342-Dose-Response Relationship, Drug,
pubmed-meshheading:11595342-Drug Interactions,
pubmed-meshheading:11595342-GABA Modulators,
pubmed-meshheading:11595342-Glutamic Acid,
pubmed-meshheading:11595342-Humans,
pubmed-meshheading:11595342-Membrane Potentials,
pubmed-meshheading:11595342-Patch-Clamp Techniques,
pubmed-meshheading:11595342-Pentobarbital,
pubmed-meshheading:11595342-Quaternary Ammonium Compounds,
pubmed-meshheading:11595342-Reaction Time,
pubmed-meshheading:11595342-Receptors, Kainic Acid,
pubmed-meshheading:11595342-Synaptic Transmission,
pubmed-meshheading:11595342-Transfection
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pubmed:year |
2001
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pubmed:articleTitle |
Pentobarbital and brilliant green modulate the current response of recombinant rat kainate-type GluR6 receptor channels differentially.
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pubmed:affiliation |
Neurological Department of the Medical School Hannover, 30623 Hannover, Germany. bufler.johannes@mh-hannover.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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