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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1996-3-14
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pubmed:abstractText |
The functional activity and selectivity of the novel 5-HT1D receptor antagonist GR 127,935 (2'-methyl-4'(5-methyl-1,2,4 oxadiazol-3-yl)-biphenyl-4-carboxylic acid [4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-amide) was investigated at cloned human 5-HT1A, 5-HT1D alpha, 5-HT1D beta and opossum kidney (OK) 5-HT1B receptor sites. 5-HT1 receptor-mediated activity was studied by measuring the inhibition of forskolin-induced cAMP formation in cell lines expressing these receptors (Bmax (fmol/mg protein): human epitheloid carcinoma HeLa/5-HT1A: 1285, OK/5-HT1B: 52, Chinese hamster ovary CHO-K1/5-HT1D alpha: 181 and CHO-K1/5-HT1D beta: 685). GR 127,935 did not show 5-HT1D beta receptor-mediated agonist activity in permanently transfected CHO-K1 cells, whereas at submicromolar and higher concentrations intrinsic agonist activity was observed in HeLa/5-HT1A,OK/5-HT1B and CHO-K1/5-HT1D alpha cells. GR 127,935 showed potent (KB value: 1.3 nM) and silent antagonism at CHO-K1/5-HT1D beta receptor sites. The antagonist activity of 1 microM of GR 127,935 at CHO-K1/5-HT1D alpha and OK/5-HT1B receptor sites was only partial and less pronounced. This contrasts with the silent antagonism of methiothepin at the 5-HT1D alpha (KB value = 11.8 nM), 5-HT1D beta (KB value = 6.9 nM) and 5-HT1B (KB value = 49.3 nM) receptor subtypes. GR 127,935, when tested at 10 microM, was found to be a weak and partial antagonist of HeLa/5-HT1A receptors.(ABSTRACT TRUNCATED AT 250 WORDS)
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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/Cyclic AMP,
http://linkedlifedata.com/resource/pubmed/chemical/Forskolin,
http://linkedlifedata.com/resource/pubmed/chemical/GR 127935,
http://linkedlifedata.com/resource/pubmed/chemical/Methiothepin,
http://linkedlifedata.com/resource/pubmed/chemical/Oxadiazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Piperazines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Spiperone
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0014-2999
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
18
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pubmed:volume |
290
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
95-103
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pubmed:dateRevised |
2005-11-17
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pubmed:meshHeading |
pubmed-meshheading:8575538-Animals,
pubmed-meshheading:8575538-CHO Cells,
pubmed-meshheading:8575538-Cricetinae,
pubmed-meshheading:8575538-Cyclic AMP,
pubmed-meshheading:8575538-Forskolin,
pubmed-meshheading:8575538-HeLa Cells,
pubmed-meshheading:8575538-Humans,
pubmed-meshheading:8575538-Methiothepin,
pubmed-meshheading:8575538-Opossums,
pubmed-meshheading:8575538-Oxadiazoles,
pubmed-meshheading:8575538-Piperazines,
pubmed-meshheading:8575538-Receptors, Serotonin,
pubmed-meshheading:8575538-Serotonin Antagonists,
pubmed-meshheading:8575538-Spiperone,
pubmed-meshheading:8575538-Transfection
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pubmed:year |
1995
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pubmed:articleTitle |
Functional effects of the 5-HT1D receptor antagonist GR 127,935 at human 5-HT1D alpha, 5-HT1D beta, 5-HT1A and opossum 5-HT1B receptors.
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pubmed:affiliation |
Laboratory of Cellular Neurobiology, Centre de Recherche Pierre Fabre, Castres, France.
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pubmed:publicationType |
Journal Article
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