Source:http://linkedlifedata.com/resource/pubmed/id/14656318
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
10
|
| pubmed:dateCreated |
2003-12-5
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| pubmed:abstractText |
Inflammation and demyelination both contribute to the neurological deficits characteristic of multiple sclerosis. Neurological dysfunctions are attributable to inflammatory demyelination and, in addition, to soluble factors such as nitric oxide, cytokines and antibodies. QYNAD, an endogenous pentapeptide identified in the cerebrospinal fluid of patients with demyelinating disorders, has been proposed to promote axonal dysfunction by blocking sodium channels. The present study aimed at characterizing the properties of QYNAD in acutely isolated thalamic neurons in vitro. QYNAD, but not a scrambled peptide (NYDQA), blocked sodium channels in neurons by shifting the steady-state inactivation to more negative potentials. Blocking properties followed a dose-response curve with a maximum effect at 10 microm. A fluorescently labelled QYNAD analogue with retained biological activity specifically stained thalamic neurons, positive for type II sodium channels, thus demonstrating the specificity of QYNAD binding. Our study confirms and extends previous observations describing QYNAD as a potent sodium channel-blocking agent. These data as well as our preliminary observations in in vivo experiments in an animal model of inflammatory CNS demyelination warrant further in vivo studies in order to clarify the exact pathogenetic role of QYNAD in inflammatory neurological diseases.
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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/Anesthetics, Local,
http://linkedlifedata.com/resource/pubmed/chemical/Oligopeptides,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Tetrodotoxin,
http://linkedlifedata.com/resource/pubmed/chemical/pentapeptide QYNAD
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| pubmed:status |
MEDLINE
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| pubmed:month |
Nov
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| pubmed:issn |
0953-816X
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
18
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
2697-706
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:14656318-Anesthetics, Local,
pubmed-meshheading:14656318-Animals,
pubmed-meshheading:14656318-Animals, Newborn,
pubmed-meshheading:14656318-Dose-Response Relationship, Drug,
pubmed-meshheading:14656318-Electrophysiology,
pubmed-meshheading:14656318-Female,
pubmed-meshheading:14656318-Geniculate Bodies,
pubmed-meshheading:14656318-Immunohistochemistry,
pubmed-meshheading:14656318-Male,
pubmed-meshheading:14656318-Mass Spectrometry,
pubmed-meshheading:14656318-Membrane Potentials,
pubmed-meshheading:14656318-Neural Conduction,
pubmed-meshheading:14656318-Neurons,
pubmed-meshheading:14656318-Oligopeptides,
pubmed-meshheading:14656318-Rats,
pubmed-meshheading:14656318-Rats, Inbred Strains,
pubmed-meshheading:14656318-Rats, Long-Evans,
pubmed-meshheading:14656318-Sodium Channels,
pubmed-meshheading:14656318-Tetrodotoxin,
pubmed-meshheading:14656318-Time Factors
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| pubmed:year |
2003
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| pubmed:articleTitle |
Modulation of neuronal activity by the endogenous pentapeptide QYNAD.
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| pubmed:affiliation |
Institute of Physiology, Otto-von-Guericke University, Magdeburg, Germany.
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| pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, Non-U.S. Gov't
|