TY - JOUR
T1 - Differential effect of metabolic alkalosis and hypoxia on high-intensity cycling performance
AU - Flinn, Samantha
AU - Herbert, Kathryn
AU - Graham, Kenneth
AU - Siegler, Jason C.
PY - 2014
Y1 - 2014
N2 - The purpose of this study was to investigate the effects of sodium bicarbonate (NaHC03) ingestion and acute hypoxic exposure on repeated bouts of high-intensity cycling to task failure. Twelve subjects completed 4 separate intermittent cycling bouts cycling bouts to task failure (120% peak power output for 30-second interspersed with 30-second active recovery) under the following conditions: normoxia (F10 2% at 20.93%) alkalosis (NA), normoxia placebo (NP), hypoxia (F10 2% at 14.7%) alkalosis (HA), and hypoxia placebo (HP). For the NA and HA trials, the buffer solution (0.3 g·kg -1 of NaHC03) was dispensed into gelatin capsules and consumed over 90 minutes with 1 L of water. Whole-blood acid-base findings demonstrated metabolic alkalosis in both NA and HA before exercise (HC03 -: 32.8 ± 1.8 mmol·L -1). Time to task failure was significantly impaired in the hypoxic conditions (NA: 199.1 ± 62.3 seconds, NP: 183.8 ± 45.0 seconds, HA: 127.8 ± 27.9 seconds, HP: 133.3 ± 28.7 seconds; p < 0.001; 112 = 0.7). There was no difference between the HA and HP conditions (p = 0.41); however the 2 normoxic conditions approached significance with the NA condition on average resulting in approximately 15-second improvement in time to task failure (p = 0.09). These findings suggest that an acute decline in F10 2% consistent with hypoxic exposure is more inhibiting than metabolic acidosis during intermittent high-intensity cycling to task failure. In application, the use of hypoxia and NaHC03 concurrently to improve performance under these conditions does not seem warranted.
AB - The purpose of this study was to investigate the effects of sodium bicarbonate (NaHC03) ingestion and acute hypoxic exposure on repeated bouts of high-intensity cycling to task failure. Twelve subjects completed 4 separate intermittent cycling bouts cycling bouts to task failure (120% peak power output for 30-second interspersed with 30-second active recovery) under the following conditions: normoxia (F10 2% at 20.93%) alkalosis (NA), normoxia placebo (NP), hypoxia (F10 2% at 14.7%) alkalosis (HA), and hypoxia placebo (HP). For the NA and HA trials, the buffer solution (0.3 g·kg -1 of NaHC03) was dispensed into gelatin capsules and consumed over 90 minutes with 1 L of water. Whole-blood acid-base findings demonstrated metabolic alkalosis in both NA and HA before exercise (HC03 -: 32.8 ± 1.8 mmol·L -1). Time to task failure was significantly impaired in the hypoxic conditions (NA: 199.1 ± 62.3 seconds, NP: 183.8 ± 45.0 seconds, HA: 127.8 ± 27.9 seconds, HP: 133.3 ± 28.7 seconds; p < 0.001; 112 = 0.7). There was no difference between the HA and HP conditions (p = 0.41); however the 2 normoxic conditions approached significance with the NA condition on average resulting in approximately 15-second improvement in time to task failure (p = 0.09). These findings suggest that an acute decline in F10 2% consistent with hypoxic exposure is more inhibiting than metabolic acidosis during intermittent high-intensity cycling to task failure. In application, the use of hypoxia and NaHC03 concurrently to improve performance under these conditions does not seem warranted.
UR - http://hdl.handle.net/1959.7/uws:24372
U2 - 10.1519/JSC.0000000000000489
DO - 10.1519/JSC.0000000000000489
M3 - Article
SN - 1064-8011
VL - 28
SP - 2852
EP - 2858
JO - Journal of Strength and Conditioning Research
JF - Journal of Strength and Conditioning Research
IS - 10
ER -