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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1990-9-18
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pubmed:abstractText |
5-Hydroxytryptamine (5-HT) and K+ induced contractions in human chorionic arteries and veins. 5-HT-caused responses were blocked by ketanserin (10(-7) and 10(-6) M) and prazosin (10(-5) but not 10(-6) M). K(+)-induced contractions were practically abolished in a Ca2(+)-free medium, whereas those produced by 5-HT were reduced. The efficacy (EC50 values) of diltiazem to produce relaxation in arteries and veins contracted with 40 or 75 mM K+ was similar, but normally greater than that of nifedipine. The potency of nifedipine (IC50 values) to inhibit maximal K+ contractions was greater than to inhibit maximal 5-HT contractions; diltiazem showed an inverse order of potency, which was less than that of nifedipine. The time course of 10(-6) M 5-HT and 75 mM K+ contractions was different, as much in the absence as in the presence of both Ca2+ antagonists; 5-HT contractions were transient, but sustained those elicited by K+. K+ (75 mM) and 5-HT (10(-6) M) produced increases in 45Ca2+ uptake, which were reduced by the Ca2+ antagonists. These results indicate that (a) human chorionic arteries and veins are similarly sensitive to Ca2+ antagonists, (b) 5-HT-induced contractions were largely dependent on extracellular Ca2+ and mainly mediated by 5-HT2 receptors but not by alpha 1-adrenoceptors, and (c) nifedipine was more potent than diltiazem in inhibiting Ca2+ influx through potential- and receptor-dependent Ca2+ channels.
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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/Calcium,
http://linkedlifedata.com/resource/pubmed/chemical/Calcium Radioisotopes,
http://linkedlifedata.com/resource/pubmed/chemical/Diltiazem,
http://linkedlifedata.com/resource/pubmed/chemical/Ketanserin,
http://linkedlifedata.com/resource/pubmed/chemical/Nifedipine,
http://linkedlifedata.com/resource/pubmed/chemical/Potassium,
http://linkedlifedata.com/resource/pubmed/chemical/Prazosin,
http://linkedlifedata.com/resource/pubmed/chemical/Serotonin
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
0160-2446
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
128-38
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1696655-Arteries,
pubmed-meshheading:1696655-Calcium,
pubmed-meshheading:1696655-Calcium Radioisotopes,
pubmed-meshheading:1696655-Diltiazem,
pubmed-meshheading:1696655-Female,
pubmed-meshheading:1696655-Humans,
pubmed-meshheading:1696655-Ketanserin,
pubmed-meshheading:1696655-Muscle, Smooth, Vascular,
pubmed-meshheading:1696655-Muscle Contraction,
pubmed-meshheading:1696655-Nifedipine,
pubmed-meshheading:1696655-Placenta,
pubmed-meshheading:1696655-Potassium,
pubmed-meshheading:1696655-Prazosin,
pubmed-meshheading:1696655-Pregnancy,
pubmed-meshheading:1696655-Regional Blood Flow,
pubmed-meshheading:1696655-Serotonin,
pubmed-meshheading:1696655-Veins
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pubmed:year |
1990
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pubmed:articleTitle |
Effects of Ca2+ antagonists nifedipine and diltiazem on isolated human chorionic arteries and veins.
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pubmed:affiliation |
Departamento de Farmcología y Terapéutica, Facultad de Medicina, Universidad de Extremadura, Madrid, Spain.
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pubmed:publicationType |
Journal Article,
Comparative Study,
In Vitro,
Research Support, Non-U.S. Gov't
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