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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1999-2-26
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pubmed:abstractText |
The nitric oxide donor hydroxylamine (NH2OH) induced a transient depression of the evoked synaptic potential recorded in the rat hippocampal CA1 region. This depression was abolished with an adenosine A1 antagonist, 8-cyclopentyltheophylline. In addition, hydroxylamine reversed adenosine A1 receptor-mediated inhibition of the evoked population spike, the fEPSP and the intracellularly recorded EPSP. The inhibitory modulation of adenosine A1 receptor activation by hydroxylamine suggests the presence of a potent endogenous regulatory site.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
0006-8993
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pubmed:author | |
pubmed:copyrightInfo |
Copyright 1999 Elsevier Science B.V.
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pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
815
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
414-8
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:9878859-Animals,
pubmed-meshheading:9878859-Excitatory Postsynaptic Potentials,
pubmed-meshheading:9878859-Hippocampus,
pubmed-meshheading:9878859-Hydroxylamine,
pubmed-meshheading:9878859-Male,
pubmed-meshheading:9878859-Neural Inhibition,
pubmed-meshheading:9878859-Neuronal Plasticity,
pubmed-meshheading:9878859-Patch-Clamp Techniques,
pubmed-meshheading:9878859-Purinergic P1 Receptor Antagonists,
pubmed-meshheading:9878859-Rats,
pubmed-meshheading:9878859-Rats, Sprague-Dawley,
pubmed-meshheading:9878859-Receptors, Purinergic P1,
pubmed-meshheading:9878859-Synaptic Transmission
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pubmed:year |
1999
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pubmed:articleTitle |
Hydroxylamine blocks adenosine A1 receptor-mediated inhibition of synaptic transmission in rat hippocampus.
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pubmed:affiliation |
Department of Physiology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.phyjcf@ttuhsc.edu
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.
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