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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1994-12-8
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pubmed:abstractText |
ATP-sensitive potassium (K+ATP) channel openers such as cromakalim and pinacidil exhibit both potent vasodilatory and anti-ischemic properties. U-89232, a cyanoguanidine analog of cromakalim, has recently been found to exhibit myocardial protection during ischemia without altering in vivo hemodynamics. We examined the effects of U-89232, cromakalim and pinacidil in isolated vascular and cardiac tissue and tested whether glyburide, a KATP channel blocker, could antagonize their effects. All three compounds produced concentration-dependent relaxation in isolated vascular segments, with cromakalim being approximately 100-fold more potent than either pinacidil or U-89232. Glyburide completely antagonized the effects of pinacidil but merely blunted the effects of cromakalim and U-89232. In an isolated rabbit cardiac tissue preparation, U-89232 had little effect on maximum tension in cardiac muscle, whereas cromakalim and pinacidil significantly decreased maximum developed tension in a concentration-dependent manner. Glyburide effectively antagonized the effects of cromakalim and pinacidil in cardiac tissue. These data suggest that U-89232, although chemically related to cromakalim, possesses activity which is not common to known potassium channel openers.
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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/Benzopyrans,
http://linkedlifedata.com/resource/pubmed/chemical/Cromakalim,
http://linkedlifedata.com/resource/pubmed/chemical/Glyburide,
http://linkedlifedata.com/resource/pubmed/chemical/Guanidines,
http://linkedlifedata.com/resource/pubmed/chemical/Pinacidil,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium Channels,
http://linkedlifedata.com/resource/pubmed/chemical/Pyrroles,
http://linkedlifedata.com/resource/pubmed/chemical/U 89232,
http://linkedlifedata.com/resource/pubmed/chemical/Vasodilator Agents
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0031-7012
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
86-95
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:7972325-Animals,
pubmed-meshheading:7972325-Benzopyrans,
pubmed-meshheading:7972325-Cromakalim,
pubmed-meshheading:7972325-Dose-Response Relationship, Drug,
pubmed-meshheading:7972325-Female,
pubmed-meshheading:7972325-Glyburide,
pubmed-meshheading:7972325-Guanidines,
pubmed-meshheading:7972325-Male,
pubmed-meshheading:7972325-Muscle, Smooth, Vascular,
pubmed-meshheading:7972325-Muscle Relaxation,
pubmed-meshheading:7972325-Myocardial Contraction,
pubmed-meshheading:7972325-Pinacidil,
pubmed-meshheading:7972325-Potassium Channels,
pubmed-meshheading:7972325-Pyrroles,
pubmed-meshheading:7972325-Rabbits,
pubmed-meshheading:7972325-Vasodilator Agents
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pubmed:year |
1994
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pubmed:articleTitle |
Comparative effects of the potassium channel openers cromakalim and pinacidil and the cromakalim analog U-89232 on isolated vascular and cardiac tissue.
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pubmed:affiliation |
Upjohn Laboratories, Upjohn Company, Kalamazoo, Mich. 49001.
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pubmed:publicationType |
Journal Article,
Comparative Study
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