Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
1990-8-13
|
pubmed:abstractText |
Several 5-hydroxytryptamine (5-HT3) receptor antagonists have been described. In addition to 5-HT3 receptor antagonist activity, many of these agents also possess gastroprokinetic activity. In the present report, we identify compound LY277359 maleate as a potent, p.o. active, highly selective 5-HT3 receptor antagonist lacking gastroprokinetic effects. LY277359 maleate was a potent and selective antagonist of 2-methyl 5-HT-induced contraction in the guinea pig ileum (KB = 1.6 nM), a response mediated by activation of 5-HT3 receptors. Given both i.v. (0.0003, 0.001 and 0.003 mg/kg) and p.o. (0.01 and 0.03 mg/kg), LY277359 maleate inhibited the bradycardic response to i.v. administered 5-HT in urethane-anesthetized rats. The duration of antagonism of 5-HT-induced bradycardia persisted beyond 6 hr after p.o. administration of LY277359 maleate (0.03 mg/kg p.o.). In contrast to its potent 5-HT3 receptor antagonist activity, LY277359 maleate, in doses up to 1 mg/kg p.o., did not affect gastric emptying in rats, suggesting minimal, if any, gastroprokinetic activity of LY277359 maleate. This is in contrast to another 5-HT3 receptor antagonist, zacopride, which did produce a marked increase in gastric emptying in rats at doses of 0.1 mg/kg p.o. and higher. LY277359 maleate (0.03 and 0.1 mg/kg i.v. and 0.07, 0.1, 0.3 and 1.0 mg/kg p.o.) did have effects consistent with other 5-HT3 antagonists, to inhibit cisplatin-evoked emesis in dogs.(ABSTRACT TRUNCATED AT 250 WORDS)
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/2-methyl-5-HT,
http://linkedlifedata.com/resource/pubmed/chemical/Benzofurans,
http://linkedlifedata.com/resource/pubmed/chemical/Bicyclo Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Bicyclo Compounds, Heterocyclic,
http://linkedlifedata.com/resource/pubmed/chemical/Bridged Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Cisplatin,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin Antagonists
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0022-3565
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
254
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
350-5
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:2366187-Animals,
pubmed-meshheading:2366187-Benzofurans,
pubmed-meshheading:2366187-Bicyclo Compounds,
pubmed-meshheading:2366187-Bicyclo Compounds, Heterocyclic,
pubmed-meshheading:2366187-Bridged Compounds,
pubmed-meshheading:2366187-Cisplatin,
pubmed-meshheading:2366187-Dogs,
pubmed-meshheading:2366187-Female,
pubmed-meshheading:2366187-Gastric Emptying,
pubmed-meshheading:2366187-Guinea Pigs,
pubmed-meshheading:2366187-Heart Rate,
pubmed-meshheading:2366187-Male,
pubmed-meshheading:2366187-Muscle Contraction,
pubmed-meshheading:2366187-Rats,
pubmed-meshheading:2366187-Rats, Inbred Strains,
pubmed-meshheading:2366187-Receptors, Serotonin,
pubmed-meshheading:2366187-Serotonin,
pubmed-meshheading:2366187-Serotonin Antagonists,
pubmed-meshheading:2366187-Vomiting
|
pubmed:year |
1990
|
pubmed:articleTitle |
LY277359 maleate: a potent and selective 5-HT3 receptor antagonist without gastroprokinetic activity.
|
pubmed:affiliation |
Lilly Research Laboratories, Eli Lilly and Company, Indianpolis, Indiana.
|
pubmed:publicationType |
Journal Article,
In Vitro
|