Abstract
Physical training affects insulin secretion and action, but there is a paucity of data on the direct effects in skeletal muscle and adipose tissue and on the effect of training in first-degree relatives (FDR) of patients with type 2 diabetes. We studied insulin action at the whole body level and peripherally in skeletal muscle and adipose tissue as well as insulin-secretory capacity in seven FDR and eight control (CON) subjects before and after 12 wk of endurance training. Training improved physical fitness. Insulin-mediated glucose uptake (GU) increased (whole body and leg; P < 0.05) after training in CON but not in FDR, whereas glucose-mediated GU increased (P < 0.05) in both groups. Adipose tissue GU was not affected by training, but it was higher (abdominal, P < 0.05; femoral, P = 0.09) in FDR compared with CON. Training increased skeletal muscle lipolysis (P < 0.05), and it was markedly higher (P < 0.05) in subcutaneous abdominal than in femoral adipose tissue and quadriceps muscle with no difference between FDR and CON. Glucose-stimulated insulin secretion was lower in FDR compared with CON, but no effect of training was seen. Glucagon-like peptide-1 stimulated insulin secretion five- to sevenfold. We conclude that insulin-secretory capacity is lower in FDR than in CON and that there is dissociation between training-induced changes in insulin secretion and insulin-mediated GU. Maximal GU rates are similar between groups and increases with physical training.
Original language | English |
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Journal | American Journal of Physiology: Endocrinology and Metabolism |
Volume | 299 |
Issue number | 1 |
Pages (from-to) | E80-91 |
Number of pages | 12 |
ISSN | 0193-1849 |
DOIs | |
Publication status | Published - 1 Jul 2010 |
Keywords
- Adipose Tissue
- Adult
- Blood Glucose
- Body Composition
- C-Peptide
- Diabetes Mellitus, Type 2
- Exercise
- Fatty Acids, Nonesterified
- Genetic Predisposition to Disease
- Glucagon-Like Peptide 1
- Glucose Clamp Technique
- Humans
- Insulin
- Lactic Acid
- Male
- Muscle, Skeletal
- Oxygen Consumption