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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1987-3-2
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pubmed:abstractText |
SK&F 93944 (temelastine), a novel histamine H1-receptor antagonist, has been studied in a variety of in vitro and in vivo test systems. SK&F 93944 was a competitive antagonist of histamine-induced contractions of guinea-pig ileum with a pA2 of 9.55 and a weak, non-competitive, inhibitor of the effects of histamine on guinea-pig atrium. In anaesthetized guinea-pigs SK&F 93944 displaced histamine bronchoconstriction dose-response curves at doses which had negligible effects on histamine tachycardia. In anaesthetized cats SK&F 93944 antagonized depressor responses to the histamine H1-receptor agonists, 2-(2-aminoethyl)pyridine and betahistine, at doses which had no effects on responses to the histamine H2-receptor agonist, dimaprit. Oral pretreatment with SK&F 93944 in conscious rats and guinea-pigs afforded protection versus the response to intradermal histamine injection. Comparative studies in each of the test systems showed that SK&F 93944 was of comparable or significantly greater potency than the standard compound, mepyramine. SK&F 93944 was found to be a weak, non-competitive antagonist of carbachol on the guinea-pig ileum but was devoid of measurable anticholinergic activity in vivo. Studies on the penetration of [14C]-SK&F 93944, labelled either in the isocytosine ring or in the butyl chain, showed that brain concentrations were very low when compared with the steady-state blood concentrations. In contrast, brain concentrations of [3H]-mepyramine exceeded blood concentrations by a factor of approximately 3. SK&F 93944 may have an advantage over classical histamine H1-receptor antagonists in that it is likely to be devoid of untoward effects on the central nervous system.
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-1201375,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-13108994,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-4021497,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-4155594,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-6114717,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-6116139,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-6148984,
http://linkedlifedata.com/resource/pubmed/commentcorrection/2879585-6230901
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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/Histamine,
http://linkedlifedata.com/resource/pubmed/chemical/Histamine H1 Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Parasympatholytics,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrilamine,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrimidinones,
http://linkedlifedata.com/resource/pubmed/chemical/temelastine
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0007-1188
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
87
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
569-78
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:2879585-Animals,
pubmed-meshheading:2879585-Autonomic Nervous System,
pubmed-meshheading:2879585-Central Nervous System,
pubmed-meshheading:2879585-Cerebrovascular Circulation,
pubmed-meshheading:2879585-Female,
pubmed-meshheading:2879585-Guinea Pigs,
pubmed-meshheading:2879585-Hemodynamics,
pubmed-meshheading:2879585-Histamine,
pubmed-meshheading:2879585-Histamine H1 Antagonists,
pubmed-meshheading:2879585-Male,
pubmed-meshheading:2879585-Parasympatholytics,
pubmed-meshheading:2879585-Pyrilamine,
pubmed-meshheading:2879585-Pyrimidinones,
pubmed-meshheading:2879585-Skin Absorption,
pubmed-meshheading:2879585-Sympathetic Nervous System
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pubmed:year |
1986
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pubmed:articleTitle |
Pharmacological studies with SK&F 93944 (temelastine), a novel histamine H1-receptor antagonist with negligible ability to penetrate the central nervous system.
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pubmed:publicationType |
Journal Article
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