Table 4.
F | CHO | |
---|---|---|
GLUT4, AU | ||
Pretest | 0.79 ± 0.10 | 0.86 ± 0.07 |
Posttest | 1.20 ± 0.16* | 1.28 ± 0.11* |
Citrate synthase, μmol · min−1 · g−1§ | ||
Pretest | 245 ± 27 | 285 ± 33 |
Posttest | 361 ± 35* | 301 ± 45 |
β-HAD, μmol · min−1 · g−1 | ||
Pretest | 133 ± 12 | 126 ± 20 |
Posttest | 179 ± 27* | 141 ± 12 |
Capillary density, number per fiber | ||
Type I fibers | ||
Pretest | 4.9 ± 0.2 | 4.9 ± 0.2 |
Posttest | 5.4 ± 0.1* | 5.6 ± 0.2* |
Type IIa fibers | ||
Pretest | 4.9 ± 0.2 | 4.8 ± 0.2 |
Posttest | 5.3 ± 0.2* | 5.5 ± 0.1* |
Data provided are means ± SE (F: n = 6–10; CHO: n = 6–10) and represent values before (pretest) and after (posttest) a 6-wk training period in either the fasted state (F) or with ample carbohydrate intake before and during the training sessions (CHO). Total GLUT4 protein content was measured by Western blotting (expressed relative to GAPDH; AU, arbitrary units), maximal mitochondrial activities of citrate synthase and β-hydroxyacyl coenzyme A dehydrogenase (β-HAD) were measured using enzymatic spectrophotometric assays, and the number of capillaries per fiber was determined by immunohistochemistry.
P < 0.05 vs. pretest.
P < 0.05, time × group effect.