Source:http://linkedlifedata.com/resource/pubmed/id/10374932
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
22
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pubmed:dateCreated |
1999-6-25
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pubmed:abstractText |
Essential hypertension is associated with an increased incidence of insulin resistance of skeletal muscle glucose transport. The present study determined if celiprolol, an antihypertensive agent with selective beta1-adrenoceptor antagonist and additional beta2-agonistic properties, administered by gavage either acutely (3 hr) or chronically (14 d), had a direct effect on improving glucose tolerance and insulin-stimulated glucose transport activity (using 2-deoxyglucose (2-DG) uptake) in isolated epitrochlearis muscles of the insulin-resistant obese Zucker rat. The effects of a selective beta1-blocker, metoprolol, were also assessed. Acute administration of celiprolol, but not metoprolol, increased insulin-stimulated 2-DG uptake in muscle by 22% (p<0.05). Chronic celiprolol treatment significantly lowered fasting plasma insulin (22%) and free fatty acids (40%) in comparison to obese control values. Moreover, chronic celiprolol administration decreased the glucose-insulin index (calculated as the product of the glucose and insulin areas under the curve during an oral glucose tolerance test), by 32% (p<0.05) compared to obese controls, indicating that peripheral insulin action was increased. Indeed, insulin-stimulated skeletal muscle 2-DG uptake was enhanced by 49% (p<0.05) in these celiprolol-treated obese animals. Metoprolol was without significant effect on any of these variables following chronic administration. These findings indicate that, in this animal model of insulin resistance, the beta1-antagonist/beta2-agonist celiprolol has a specific effect of improving insulin-stimulated skeletal muscle glucose transport that is independent of any hemodynamic alterations.
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pubmed:keyword | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Adrenergic beta-Antagonists,
http://linkedlifedata.com/resource/pubmed/chemical/Antihypertensive Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Celiprolol,
http://linkedlifedata.com/resource/pubmed/chemical/Deoxyglucose,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Metoprolol
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pubmed:status |
MEDLINE
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pubmed:issn |
0024-3205
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
64
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2071-9
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:10374932-Adrenergic beta-Antagonists,
pubmed-meshheading:10374932-Animals,
pubmed-meshheading:10374932-Antihypertensive Agents,
pubmed-meshheading:10374932-Biological Transport, Active,
pubmed-meshheading:10374932-Blood Glucose,
pubmed-meshheading:10374932-Celiprolol,
pubmed-meshheading:10374932-Deoxyglucose,
pubmed-meshheading:10374932-Female,
pubmed-meshheading:10374932-Hypertension,
pubmed-meshheading:10374932-Insulin,
pubmed-meshheading:10374932-Insulin Resistance,
pubmed-meshheading:10374932-Metoprolol,
pubmed-meshheading:10374932-Muscle, Skeletal,
pubmed-meshheading:10374932-Obesity,
pubmed-meshheading:10374932-Rats,
pubmed-meshheading:10374932-Rats, Zucker
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pubmed:year |
1999
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pubmed:articleTitle |
The beta2-adrenergic modulator celiprolol reduces insulin resistance in obese Zucker rats.
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pubmed:affiliation |
Department of Endocrinology, Eberhard-Karls University, Tübingen, Germany.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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