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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1989-6-27
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pubmed:abstractText |
In addition to the 5-HT3-mediated fast depolarisation, 5-hydroxytryptamine (5-HT) evoked two additional responses on the rat superior cervical ganglion: a hyperpolarisation and a slow depolarisation. These responses appeared to be direct actions on 5-HT receptors since they were present in a low calcium medium containing tetrodotoxin and were not abolished by a variety of non-serotonin antagonists. The hyperpolarisation was not antagonised by 5-HT3 or 5-HT2 antagonists. The 5-HT1 ligands 5-carboxamidotryptamine (5-CT) and 8-OH-DPAT also evoked a hyperpolarisation. The hyperpolarisation was antagonised by six 5-HT1A antagonists including WB-4101 and spiroxatrine. It was therefore concluded to be mediated by a 5-HT1A receptor. The slow depolarisation was only evoked by 5-HT. The receptor involved in this response, however, could not be determined. We conclude that in addition to 5-HT3 receptors the rat superior cervical ganglion possesses 5-HT1A receptors and another uncharacterised 5-HT receptor.
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pubmed:commentsCorrections | |
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 |
Mar
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pubmed:issn |
0014-2999
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
21
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pubmed:volume |
162
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
197-205
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2721566-Animals,
pubmed-meshheading:2721566-Ganglia, Spinal,
pubmed-meshheading:2721566-Male,
pubmed-meshheading:2721566-Neuromuscular Depolarizing Agents,
pubmed-meshheading:2721566-Rats,
pubmed-meshheading:2721566-Rats, Inbred Strains,
pubmed-meshheading:2721566-Serotonin,
pubmed-meshheading:2721566-Serotonin Antagonists
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pubmed:year |
1989
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pubmed:articleTitle |
5-Hydroxytryptamine evokes three distinct responses on the rat superior cervical ganglion in vitro.
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pubmed:affiliation |
Merck Sharp and Dohme Research Laboratories, Neuroscience Research Centre, Essex, U.K.
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pubmed:publicationType |
Journal Article,
In Vitro
|