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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
1997-4-22
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pubmed:abstractText |
Eight fit men [maximum oxygen consumption (VO2max) 64.6 (1.9) ml x kg(-1)xmin(-1), aged 28.3 (1.7) years (SE in parentheses) were studied during two treadmill exercise trials to determine the effect of endogenous opioids on insulin and glucagon immunoreactivity during intense exercise (80% VO2max). A double-blind experimental design was used with subjects undertaking the two exercise trials in counterbalanced order. Exercise trials were 20 min in duration and were conducted 7 days apart. One exercise trial was undertaken following administration of naloxone (N; 1.2 mg; 3 ml) and the other after receiving a placebo (P; 0.9% NaCl saline; 3 ml). Prior to each experimental trial a flexible catheter was placed into an antecubital vein and baseline blood samples were collected. Immediately after, each subject received either a N or P bolus injection. Blood samples were also collected after 20 min of continuous exercise (running). Glucagon was higher (P < 0.05), while insulin was lower (P < 0.05), during exercise compared with pre-exercise values in both trials. However, glucagon was higher (P < 0.05) in the P than in the N exercise trial [141.4 (8.3) ng x 1(-1) vs 127.2 (7.6) ng x 1(-1)]. There were no differences in insulin during exercise between the P and N trials [50.2 (4.3) pmol x 1(-1) vs 43.8 (5) pmol x 1(-1)]. These data suggest that endogenous opioids may augment the glucagon response during intense exercise.
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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:issn |
0301-5548
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
132-5
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading | |
pubmed:year |
1997
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pubmed:articleTitle |
Insulin and glucagon immunoreactivity during high-intensity exercise under opiate blockade.
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pubmed:affiliation |
Laboratory of Applied Physiology, The University of Southern Mississippi, Hattiesburg 39406, USA.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Randomized Controlled Trial,
Research Support, Non-U.S. Gov't
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