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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0003765,
umls-concept:C0017687,
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0021641,
umls-concept:C0037659,
umls-concept:C0086418,
umls-concept:C0311400,
umls-concept:C0441800,
umls-concept:C0574032,
umls-concept:C0871261,
umls-concept:C1280500,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
10
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pubmed:dateCreated |
1993-11-9
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pubmed:abstractText |
Insulin inhibits its own release (autofeedback), and growth hormone (GH) inhibits the GH response to a variety of stimuli. The aim of this study was to evaluate whether glucagon (G) can modify pancreatic G (IRG) release in humans. Seven healthy men received intravenous (i.v.) arginine (30 g in 30 minutes) 240 minutes after the beginning of a 0.9% NaCI saline infusion and a 2.5-, 4.0-, and 8.0-ng/kg.min-1 porcine G infusion, with each infusion lasting 360 minutes. All G infusions yielded stable and dose-related plasma IRG levels, and the 4.0- and 8.0-ng/kg.min-1 G infusions decreased plasma free fatty acids (FFA) and blood glycerol and beta-OH-butyrate levels and elicited insulin (IRI) release, and the 8.0-ng/kg.min-1 G infusion elicited GH release and increased blood glucose (BG) levels; somatostatin (SRIF) levels were not affected by G infusions. At 240 minutes, plasma IRG levels were higher during G infusion than during saline infusion, whereas serum IRI and BG levels had returned to preinfusion levels. At this point, G infusions decreased the integrated (240 to 300 minutes) IRG, IRI, BG, and SRIF responses, but not the GH response to arginine. These data indicate that prolonged G infusions decrease the IRG response to arginine; in addition, G decreases plasma FFA levels, and higher G doses stimulate IRI release and exert a self-limited hyperglycemic effect. The fact that the IRI response to arginine was decreased by G could be due to a refractoriness of beta cells to subsequent stimuli; the decreased SRIF response to arginine is likely due to G itself or to a decrease of plasma FFA levels.
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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/3-Hydroxybutyric Acid,
http://linkedlifedata.com/resource/pubmed/chemical/Arginine,
http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/Fatty Acids, Nonesterified,
http://linkedlifedata.com/resource/pubmed/chemical/Glucagon,
http://linkedlifedata.com/resource/pubmed/chemical/Glycerol,
http://linkedlifedata.com/resource/pubmed/chemical/Growth Hormone,
http://linkedlifedata.com/resource/pubmed/chemical/Hydroxybutyrates,
http://linkedlifedata.com/resource/pubmed/chemical/Insulin,
http://linkedlifedata.com/resource/pubmed/chemical/Somatostatin
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0026-0495
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1242-8
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:8105365-3-Hydroxybutyric Acid,
pubmed-meshheading:8105365-Adult,
pubmed-meshheading:8105365-Arginine,
pubmed-meshheading:8105365-Blood Glucose,
pubmed-meshheading:8105365-Dose-Response Relationship, Drug,
pubmed-meshheading:8105365-Fatty Acids, Nonesterified,
pubmed-meshheading:8105365-Feedback,
pubmed-meshheading:8105365-Glucagon,
pubmed-meshheading:8105365-Glycerol,
pubmed-meshheading:8105365-Growth Hormone,
pubmed-meshheading:8105365-Humans,
pubmed-meshheading:8105365-Hydroxybutyrates,
pubmed-meshheading:8105365-Infusions, Intravenous,
pubmed-meshheading:8105365-Insulin,
pubmed-meshheading:8105365-Male,
pubmed-meshheading:8105365-Radioimmunoassay,
pubmed-meshheading:8105365-Somatostatin,
pubmed-meshheading:8105365-Time Factors
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pubmed:year |
1993
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pubmed:articleTitle |
Metabolic effects of graded glucagon infusions in man: inhibition of glucagon, insulin, and somatostatin response to arginine.
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pubmed:affiliation |
Istituto Scientifico San Raffaele, Milan, Italy.
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pubmed:publicationType |
Journal Article
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