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Swim training increases glucose output from liver perfused in situ with glucagon in fed and fasted rats
The effect of endurance swim training (3 hours per day, 5 days/week, for 10 weeks) on hepatic glucose production (HGP) in liver perfused in situ for 60 minutes with glucagon and insulin was studied in Sprague-Dawley rats. The experiments were performed in fed rats and in rats fasted for 24 hours, bu...
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Published in: | Metabolism, clinical and experimental clinical and experimental, 2004-08, Vol.53 (8), p.1027-1031 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The effect of endurance swim training (3 hours per day, 5 days/week, for 10 weeks) on hepatic glucose production (HGP) in liver perfused in situ for 60 minutes with glucagon and insulin was studied in Sprague-Dawley rats. The experiments were performed in fed rats and in rats fasted for 24 hours, but with lactate (8 mmol/L) added to the perfusion medium. Liver glycogen content was significantly lower in fasted than fed rats (fasted untrained and trained: 14 ± 4 and 11 ± 3 μmol glycosyl U/g of liver wet weight (WW); fed untrained and trained: 205 ± 11 and 231 ± 11 μmol glycosyl U/g of liver WW; not significantly different in trained and untrained rats). Glucagon increased HGP in the 4 experimental groups, but the increases were more rapid and pronounced in trained than in untrained rats in both fed and fasted states. HGP values (area under the curve [AUC] in μmol/g of liver WW) were significantly higher in trained fed (112.1 ± 7.1
v 85.9 ± 12.2 in untrained rats) than in trained fasted rats (50.8 ± 4.4
v 34.7 ± 3.6 in untrained rats). When compared with untrained rats, the total amount of glucose released by the liver in response to glucagon in trained rats was approximately 30% higher in the fed state and approximately 45% larger in the fasted state. These results indicate that endurance training increases the response of both glycogenolysis and gluconeogenesis to glucagon. |
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ISSN: | 0026-0495 1532-8600 |
DOI: | 10.1016/j.metabol.2004.03.010 |