Insulin-dependent glycogen synthesis is delayed in onset in the skeletal muscle of food-deprived aged rats
Insulin resistance with aging may be responsible for impaired glycogen synthesis in the skeletal muscle of aged rats and contribute to the well-known decreased ability to respond to stress with aging. For this reason, to assess the ability of the skeletal muscle to utilize glucose for glycogen synth...
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Published in | The Journal of nutritional biochemistry Vol. 16; no. 3; pp. 150 - 154 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Elsevier Inc
01.03.2005
Elsevier Science Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | Insulin resistance with aging may be responsible for impaired glycogen synthesis in the skeletal muscle of aged rats and contribute to the well-known decreased ability to respond to stress with aging. For this reason, to assess the ability of the skeletal muscle to utilize glucose for glycogen synthesis during aging, the time course of glycogen synthesis was continuously monitored by
13C nuclear magnetic resonance for 2 h in isolated [
13C] glucose-perfused gastrocnemius–plantaris muscles of 5-day food-deprived adult (6–8 months;
n=10) or 5-day food-deprived aged (22 months;
n=8) rats. [
13C] glucose (10 mmol/L) perfusion was carried out in the presence or absence of an excess of insulin (1 μmol/L). Food deprivation only decreased glycogen level in adult rats (8.9±2.4 μmol/g in adults vs. 35.6±2.4 μmol/g in aged rats;
P<.05). In the presence of an excess of insulin, muscle glycogen synthesis was stimulated in both adult and aged muscles, but the onset was delayed with aging (40 min later). In conclusion, this study highlights the important role of glycogen depletion in stimulating glycogen synthesis in muscles. Consequently, the absence of glycogen depletion in response to starvation in aged rats may be the origin of the delay in insulin-stimulated glycogen synthesis in the skeletal muscle. Glycogen synthesis clearly was not impaired with aging. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0955-2863 1873-4847 |
DOI: | 10.1016/j.jnutbio.2004.12.001 |