Source:http://linkedlifedata.com/resource/pubmed/id/18198343
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2008-3-18
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pubmed:abstractText |
5-Hydroxytryptamine (5-HT) receptors and dopamine(2) (D(2)) receptor modulate gastrointestinal motility. Gastroprokinetic agents that act on several 5-HT receptor subtypes and/or D(2) receptors are used clinically. Although the 5-HT(4) receptor is known to mediate the gastroprokinetic effects of these agents, the absence of highly selective 5-HT(4) receptor agonists has made it difficult to confirm the physiological consequences of selective 5-HT(4) receptor stimulation. In this study, we report the in vitro pharmacological profiles and the in vivo gastroprokinetic effects of 5-amino-6-chloro-N-[(1-isobutylpiperidin-4-yl)methyl]-2-methylimidazo[1,2-alpha]pyridine-8-carboxamide (CJ-033,466), a novel, potent, and selective 5-HT(4) partial agonist. Compared with preceding 5-HT(4) agonists such as cisapride, mosapride, and tegaserod, CJ-033,466 had a superior in vitro profile, with nanomolar agonistic activities for the 5-HT(4) receptor and 1000-fold greater selectivity for the 5-HT(4) receptor over other 5-HT and D(2) receptors. In vivo studies in conscious dogs showed that CJ-033,466 dose-dependently stimulated gastric antral motility in both the fasted and postprandial states at the same dose range and that it was 30 times more potent than cisapride. Furthermore, CJ-033,466 accelerated the gastric emptying rate in a gastroparesis dog model at the minimally effective dose established in the gastric motility study. In conclusion, CJ-033,466 is a potent and highly selective 5-HT(4) agonist that stimulates physiologically coordinated gastric motility, and it has no activity on other 5-HT receptor subtypes and D(2) receptors. Therefore, CJ-033,466 could be used to treat gastroparesis, providing better gastroprokinetics and reduced side effects mediated by the other receptors.
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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/Aminopyridines,
http://linkedlifedata.com/resource/pubmed/chemical/CJ 033466,
http://linkedlifedata.com/resource/pubmed/chemical/Imidazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Dopamine D2,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin 5-HT4 Receptor Agonists,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Receptor Agonists
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1521-0103
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
325
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
190-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:18198343-Aminopyridines,
pubmed-meshheading:18198343-Animals,
pubmed-meshheading:18198343-Dogs,
pubmed-meshheading:18198343-Dose-Response Relationship, Drug,
pubmed-meshheading:18198343-Gastric Emptying,
pubmed-meshheading:18198343-Gastrointestinal Motility,
pubmed-meshheading:18198343-Gastroparesis,
pubmed-meshheading:18198343-Humans,
pubmed-meshheading:18198343-Imidazoles,
pubmed-meshheading:18198343-Radioligand Assay,
pubmed-meshheading:18198343-Rats,
pubmed-meshheading:18198343-Receptors, Dopamine D2,
pubmed-meshheading:18198343-Serotonin 5-HT4 Receptor Agonists,
pubmed-meshheading:18198343-Serotonin Receptor Agonists
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pubmed:year |
2008
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pubmed:articleTitle |
5-Amino-6-chloro-N-[(1-isobutylpiperidin-4-yl)methyl]-2-methylimidazo[1,2-alpha]pyridine-8-carboxamide (CJ-033,466), a novel and selective 5-hydroxytryptamine4 receptor partial agonist: pharmacological profile in vitro and gastroprokinetic effect in conscious dogs.
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pubmed:affiliation |
Drug Safety Research and Development, Tokyo Laboratories, Pfizer Global Research and Development, Pfizer Inc., 3-22-7 Yoyogi, Shibuya, Tokyo 151-8589, Japan.
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pubmed:publicationType |
Journal Article
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