TABLE 2.
Body composition and resting metabolic rate (RMR) before and after 28 d of placebo or dihydrocapsiate ingestion1
| Placebo (n = 28) |
3 mg dihydrocapsiate (n = 25) |
9 mg dihydrocapsiate (n = 25) |
Effect (P value) |
||||||
| Day 0 | Day 28 | Day 0 | Day 28 | Day 0 | Day 28 | Acute | Chronic | Dose | |
| Fat-free mass (kg) | 67.6 ± 1.8 | 67.7 ± 1.8 | 69.5 ± 1.5 | 69.9 ± 1.5 | 66.8 ± 1.4 | 67.1 ± 1.4 | — | 0.07 | 0.47 |
| Fat mass (kg) | 23.4 ± 1.4 | 23.7 ± 1.4 | 22.9 ± 1.2 | 23.2 ± 1.1 | 24.0 ± 1.3 | 24.4 ± 1.3 | — | 0.002 | 0.81 |
| RMR | |||||||||
| Before pill ingestion (kcal/d) | 1714 ± 41 | 1700 ± 43 | 1760 ± 41 | 1792 ± 39 | 1694 ± 38 | 1723 ± 35 | 0.003 | 0.19 | 0.22 |
| After pill ingestion (kcal/d) | 1717 ± 40 | 1716 ± 37 | 1800 ± 39 | 1817 ± 42 | 1749 ± 31 | 1755 ± 39 | |||
| Acute thermogenic effect (kcal/d) | 3 ± 24 | 17 ± 19 | 41 ± 17 | 25 ± 21 | 55 ± 17 | 31 ± 16 | — | 0.56 | 0.27 |
| Total AUC (kcal × min/d) | 205,654 ± 4713 | 205,637 ± 4511 | 215,481 ± 4670 | 217,217 ± 4952 | 207,931 ± 4079 | 210,107 ± 4535 | — | 0.43 | 0.21 |
| Nonprotein RQ | |||||||||
| Before pill ingestion | 0.84 ± 0.01 | 0.85 ± 0.01 | 0.83 ± 0.01 | 0.85 ± 0.01 | 0.83 ± 0.01 | 0.85 ± 0.01 | <0.001 | <0.0001 | 0.73 |
| After pill ingestion | 0.83 ± 0.01 | 0.84 ± 0.01 | 0.82 ± 0.01 | 0.84 ± 0.01 | 0.83 ± 0.01 | 0.83 ± 0.01 | |||
| Total AUC (min) | 100 ± 1 | 101 ± 1 | 99 ± 1 | 101 ± 1 | 99 ± 1 | 100 ± 1 | — | 0.005 | 0.79 |
| Fat oxidation (g/d) | |||||||||
| Before pill ingestion | 68 ± 5 | 60 ± 5 | 72 ± 5 | 67 ± 6 | 68 ± 7 | 65 ± 6 | <0.001 | 0.002 | 0.44 |
| After pill ingestion | 74 ± 4 | 69 ± 5 | 83 ± 5 | 75 ± 5 | 76 ± 5 | 77 ± 5 | |||
| Total AUC (g × min/d) | 8831 ± 482 | 8189 ± 539 | 9854 ± 563 | 8876 ± 634 | 8749 ± 604 | 9077 ± 613 | — | 0.20 | 0.47 |
All values are means ± SEs. RQ, respiratory quotient; AUC, area under the curve after pill ingestion. Metabolic variables were analyzed with the mixed model. Data were analyzed by using covariance analysis (PROC MIXED; SAS Institute, Cary, NC) with dose (0, 3, and 9 mg), acute consumption (before or after taking pill), and chronic consumption (days 1 and 28) and their interactions as fixed effects, whereas the subject nested within dose was the random effect. Fat and fat-free masses used similar analyses without acute effect.