Source:http://linkedlifedata.com/resource/pubmed/id/11282215
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2001-4-3
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pubmed:abstractText |
Electrical field stimulation (4 Hz, 0.2 ms, 70 V supramaximal voltage, 10 s duration) produced contraction of perfused rabbit central ear arteries, and this contraction was reduced by incubation with insulin (0.6--200 mU/ml). This inhibitory effect of insulin was not significantly modified by removing the endothelium, or by treatment with N(W)-nitro-L-arginine (L-NA, 10(-4) M), meclofenamate (10(-5) M), ouabain (10(-6) M), or cocaine (10(-5) M). Insulin (200 mU/ml) did not modify the vascular contraction due to exogenous norepinephrine (10(-8)--10(-4) M) nor the relaxation due to acetylcholine (10(-8)--10(-4) M). This suggests that insulin may reduce vascular contraction by sympathetic stimulation, and this effect is not dependent on endothelial nitric oxide, prostanoids, or Na(+)--K(+) pump activation.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0306-3623
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
34
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
221-6
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:11282215-Acetylcholine,
pubmed-meshheading:11282215-Animals,
pubmed-meshheading:11282215-Arteries,
pubmed-meshheading:11282215-Dose-Response Relationship, Drug,
pubmed-meshheading:11282215-Drug Interactions,
pubmed-meshheading:11282215-Ear,
pubmed-meshheading:11282215-Electric Stimulation,
pubmed-meshheading:11282215-Insulin,
pubmed-meshheading:11282215-Norepinephrine,
pubmed-meshheading:11282215-Rabbits,
pubmed-meshheading:11282215-Sympathetic Nervous System,
pubmed-meshheading:11282215-Vasoconstriction,
pubmed-meshheading:11282215-Vasoconstrictor Agents
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pubmed:year |
2000
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pubmed:articleTitle |
Insulin effects on the sympathetic contraction of rabbit ear arteries.
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pubmed:affiliation |
Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma, Arzobispo Morcillo, 2, 28029 Madrid, Spain. angeluis.villalon@uam.es
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, Non-U.S. Gov't
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