Source:http://linkedlifedata.com/resource/pubmed/id/12196558
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
17
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| pubmed:dateCreated |
2002-8-27
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| pubmed:abstractText |
Selectively reducing the excitability of specific neurons will (1) allow for the creation of animal models of human neurological disorders and (2) provide insight into the global function of specific sets of neurons. We focus on a combined genetic and pharmacological approach to silence neurons electrically. We express invertebrate ivermectin (IVM)-sensitive chloride channels (Caenorhabditis elegans GluCl alpha and beta) with a Sindbis virus and then activate these channels with IVM to produce inhibition via a Cl- conductance. We constructed a three-cistron Sindbis virus that expresses the alpha and beta subunits of a glutamate-gated chloride channel (GluCl) along with the green fluorescent protein (EGFP) marker. Expression of the C. elegans channel does not affect the normal spike activity or GABA/glutamate postsynaptic currents of cultured embryonic day 18 hippocampal neurons. At concentrations as low as 5 nm, IVM activates a Cl- current large enough to silence infected neurons effectively. This conductance reverses in 8 hr. These low concentrations of IVM do not potentiate GABA responses. Comparable results are observed with plasmid transfection of yellow fluorescent protein-tagged (EYFP) GluCl alpha and cyan fluorescent protein-tagged (ECFP) GluCl beta. The present study provides an in vitro model mimicking conditions that can be obtained in transgenic mice and in viral-mediated gene therapy. These experiments demonstrate the feasibility of using invertebrate ligand-activated Cl- channels as an approach to modulate excitability.
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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/Chloride Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorides,
http://linkedlifedata.com/resource/pubmed/chemical/Glutamic Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Ivermectin,
http://linkedlifedata.com/resource/pubmed/chemical/Ligands,
http://linkedlifedata.com/resource/pubmed/chemical/Luminescent Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/gamma-Aminobutyric Acid
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| pubmed:status |
MEDLINE
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| pubmed:month |
Sep
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| pubmed:issn |
1529-2401
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| pubmed:author | |
| pubmed:issnType |
Electronic
|
| pubmed:day |
1
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| pubmed:volume |
22
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
7373-9
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| pubmed:dateRevised |
2007-11-14
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| pubmed:meshHeading |
pubmed-meshheading:12196558-Action Potentials,
pubmed-meshheading:12196558-Animals,
pubmed-meshheading:12196558-Caenorhabditis elegans,
pubmed-meshheading:12196558-Cells, Cultured,
pubmed-meshheading:12196558-Chloride Channels,
pubmed-meshheading:12196558-Chlorides,
pubmed-meshheading:12196558-Electric Stimulation,
pubmed-meshheading:12196558-Feasibility Studies,
pubmed-meshheading:12196558-Genes, Reporter,
pubmed-meshheading:12196558-Genetic Vectors,
pubmed-meshheading:12196558-Glutamic Acid,
pubmed-meshheading:12196558-Humans,
pubmed-meshheading:12196558-Ion Channel Gating,
pubmed-meshheading:12196558-Ivermectin,
pubmed-meshheading:12196558-Kidney,
pubmed-meshheading:12196558-Ligands,
pubmed-meshheading:12196558-Luminescent Proteins,
pubmed-meshheading:12196558-Neural Inhibition,
pubmed-meshheading:12196558-Neurons,
pubmed-meshheading:12196558-Patch-Clamp Techniques,
pubmed-meshheading:12196558-Rats,
pubmed-meshheading:12196558-Sindbis Virus,
pubmed-meshheading:12196558-Synaptic Transmission,
pubmed-meshheading:12196558-Transfection,
pubmed-meshheading:12196558-gamma-Aminobutyric Acid
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| pubmed:year |
2002
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| pubmed:articleTitle |
Selective electrical silencing of mammalian neurons in vitro by the use of invertebrate ligand-gated chloride channels.
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| pubmed:affiliation |
Computation and Neural Systems Program and Division of Biology, California Institute of Technology, Pasadena, California 91125, USA.
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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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