The effects of breathing a helium–oxygen gas mixture on maximal pulmonary ventilation and maximal oxygen consumption during exercise in acute moderate hypobaric hypoxia

To test the hypothesis that maximal exercise pulmonary ventilation ( $ \dot{V}{\text{E}}_{ \max } $ ) is a limiting factor affecting maximal oxygen uptake ( $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ ) in moderate hypobaric hypoxia (H), we examined the effect of breathing a helium–oxygen gas mixture (He–O₂; 20.9% O₂), which would reduce air density and would be expected to increase $ \dot{V}{\text{E}}_{ \max } $ . Fourteen healthy young male subjects performed incremental treadmill running tests to exhaustion in normobaric normoxia (N; sea level) and in H (atmospheric pressure equivalent to 2,500 m above sea level). These exercise tests were carried out under three conditions [H with He–O₂, H with normal air and N] in random order. $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ and arterial oxy-hemoglobin saturation (SaO₂) were, respectively, 15.2, 7.5 and 4.0% higher (all p < 0.05) with He–O₂ than with normal air ( $ \dot{V}{\text{E}}_{ \max } $ _, 171.9 ± 16.1 vs. 150.1 ± 16.9 L/min; $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ , 52.50 ± 9.13 vs. 48.72 ± 5.35 mL/kg/min; arterial oxyhemoglobin saturation (SaO₂), 79 ± 3 vs. 76 ± 3%). There was a linear relationship between the increment in $ \dot{V}{\text{E}}_{ \max } $ and the increment in $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ in H (r = 0.77; p < 0.05). When subjects were divided into two groups based on their $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ , both groups showed increased $ \dot{V}{\text{E}}_{ \max } $ and SaO₂ in H with He–O₂, but $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ was increased only in the high $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ group. These findings suggest that in acute moderate hypobaric hypoxia, air-flow resistance can be a limiting factor affecting $ \dot{V}{\text{E}}_{ \max } $ ; consequently, $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ is limited in part by $ \dot{V}{\text{E}}_{ \max } $ , especially in subjects with high $ \dot{V}{\text{O}}_{{ 2 {\text{max}}}} $ .     

The validity of the Moxus Modular metabolic system during incremental exercise tests: impacts on detection of small changes in oxygen consumption

Purpose

We investigated the accuracy of the Moxus Modular Metabolic System (MOXUS) against the Douglas Bag Method (DBM) during high-intensity exercise, and whether the two methods agreed when detecting small changes in $\dot{V}{\text{O}}_{2}$ between two consecutive workloads ( $\Delta {\dot{{V}}\text{O}}_{ 2}$ ).

Methods

Twelve trained male runners performed two maximal incremental running tests while gas exchange was analyzed simultaneously by the two systems using a serial setup for four consecutive intervals of 30 s on each test. Comparisons between methods were performed for $\dot{V}{\text{O}}_{2}$ , ${\dot{{V}}}_{\text{E}}$ , fractions of expired O₂ (FeO₂) and CO₂ (FeCO₂) and $\Delta {\dot{{V}}\text{O}}_{ 2}$ .

Results

The MOXUS produced significant higher (mean ± SD, n = 54) readings for $\dot{V}{\text{O}}_{2}$ (80 ± 200 mL min^?1, p = 0.005) and ${\dot{{V}}}_{\text{E}}$ (2.9 ± 4.2 L min^?1, p < 0.0001), but not FeO₂ (?0.01 ± 0.09). Log-transformed 95 % limits of agreement for readings between methods were 94–110 % for $\dot{V}{\text{O}}_{2}$ , 97–108 % for $\dot{V}_{\text{E}}$ and 99–101 % for FeO₂. $\Delta \dot{V}{\text{O}}_{2}$ for two consecutive measurements was not different between systems (120 ± 110 vs. 90 ± 190 mL min^?1 for MOXUS and DBM, respectively, p = 0.26), but agreement between methods was very low (r = 0.25, p = 0.12).

Discussion

Although it was tested during high-intensity exercise and short sampling intervals, the MOXUS performed within the acceptable range of accuracy reported for automated analyzers. Most of the differences between equipments were due to differences in $\dot{V}_{\text{E}}$ . Detecting small changes in $\dot{V}{\text{O}}_{2}$ during an incremental test with small changes in workload, however, might be beyond the equipment’s accuracy.     

The role of anticipatory postural adjustments in interlimb coordination of coupled arm movements in the parasagittal plane: III. Difference in the energy cost of postural actions during cyclic flexion–extension arm movements, ISO- and ANTI-directionally coupled

When oscillating the upper limbs together in the parasagittal plane, movements coordination is lower (i.e., variability of the interlimb relative phase is higher) in antidirectional (ANTI) than in isodirectional (ISO) coupling. In contrast, we previously observed that for arm movements in the horizontal plane, the coordination was worse in ISO than ANTI and the energetic cost of postural activities was higher in ISO. Having hypothesised that the higher postural cost was one factor responsible for the coordination deficit in horizontal ISO, we measured the oxygen uptake ( $\dot{V}_{{{\text{O}}_{2} }}$ ) in parasagittal movements, expecting that in this case too, the postural cost is higher in the less-coordinated mode (ANTI). Breath-by-breath metabolic ( $\dot{V}_{{{\text{O}}_{ 2} }}$ , $\dot{V}_{{{\text{CO}}_{ 2} }}$ ) and cardiorespiratory (HR, $\dot{V}_{\text{E}}$ ) parameters were measured in seven participants, who performed cyclic flexions–extensions in the parasagittal plane with either one arm or both arms, in ISO or ANTI coupling and at 1.4, 2.2 and 2.6 Hz. In each condition, the intermittent exercise (12 s movement, 12 s rest) lasted 264 s. A force platform recorded the mechanical actions to the ground. The exercise metabolic cost ( $\Updelta \dot{V}_{{{\text{O}}_{ 2} }}$ ) was found to be significantly higher in parasagittal ANTI than ISO. The movement amplitude being equal in the two modes, the ANTI-ISO difference should be ascribed to postural activities. This would confirm that the less-coordinated coupling mode requires the higher postural effort in parasagittal movements too. When rising the movement frequency, $\Updelta \dot{V}_{{{\text{O}}_{ 2} }}$ increased and linearly correlated with the coordination loss. Comparison of parasagittal with horizontal movements showed that $\Updelta \dot{V}_{{{\text{O}}_{ 2} }}$ was lower in parasagittal ANTI than in horizontal ISO (the less-coordinated modes), while it was not different between parasagittal ISO and horizontal ANTI (the more-coordinated modes).     

Skeletal muscle \dot{V} {\text{O}_2} kinetics from cardio-pulmonary measurements: assessing distortions through O2 transport by means of stochastic work-rate signals and circulatory modelling

During non-steady-state exercise, dynamic changes in pulmonary oxygen uptake ( $\dot{V} {\text{O}_{\text{2pulm}}}$ ) are dissociated from skeletal muscle $ \dot{V} {\text{O}_2}$ ( $\dot{V} {\text{O}_{\text{2musc}}}$ ) by changes in lung and venous O₂ concentrations (CvO₂), and the dynamics and distribution of cardiac output (CO) between active muscle and remaining tissues ( $ \dot{Q}_{\text{rem}}$ ). Algorithms can compensate for fluctuations in lung O₂ stores, but the influences of CO and CvO₂ kinetics complicate estimation of $\dot{V} {\text{O}_{\text{2musc}}}$ from cardio-pulmonary measurements. We developed an algorithm to estimate $\dot{V} {\text{O}_{\text{2musc}}}$ kinetics from $\dot{V} {\text{O}_{\text{2pulm}}}$ and heart rate (HR) during exercise. 17 healthy volunteers (28 ± 7 years; 71 ± 12 kg; 7 females) performed incremental exercise using recumbent cycle ergometry ( $\dot{V} {\text{O}_{\text{2peak}}}$ 52 ± 8 ml min^?1 kg^?1). Participants completed a pseudo-random binary sequence (PRBS) test between 30 and 80 W. $\dot{V} {\text{O}_{\text{2pulm}}}$ and HR were measured, and CO was estimated from HR changes and steady-state stroke volume. $\dot{V} {\text{O}_{\text{2musc}}}$ was derived from a circulatory model and time series analyses, by solving for the unique combination of venous volume and the perfusion of non-exercising tissues that provided close to mono-exponential $\dot{V} {\text{O}_{\text{2musc}}}$ kinetics. Independent simulations showed that this approach recovered the $\dot{V} {\text{O}_{\text{2musc}}}$ time constant (τ) to within 7 % (R ² = 0.976). Estimates during PRBS were venous volume 2.96 ± 0.54 L; $ \dot{Q}_{\text{rem}}$ 3.63 ± 1.61 L min^?1; τHR 27 ± 11 s; τ $\dot{V} {\text{O}_{\text{2musc}}}$ 33 ± 8 s; τ $\dot{V} {\text{O}_{\text{2pulm}}}$ 43 ± 14 s; $\dot{V} {\text{O}_{\text{2pulm}}}$ time delay 19 ± 8 s. The combination of stochastic test signals, time series analyses, and a circulatory model permitted non-invasive estimates of $\dot{V} {\text{O}_{\text{2musc}}}$ kinetics. Large kinetic dissociations exist between muscular and pulmonary $\dot{V} {\text{O}_{\text{2}}}$ during rapid exercise transients.     

How long does it take to achieve steady state for an accurate assessment of resting \dot{\text{V}}{\text{O}}_{2} in healthy men?

The time necessary to obtain a steady state for an accurate and reliable assessment of resting $ \dot{V}{\text{O}}_{2} $ remains unclear and was the purpose of this study. Thirty healthy men, aged 17–28 years, visited the laboratory twice for the assessment of resting $ \dot{V}{\text{O}}_{2} $ , which was assessed as follows: (a) 24 h abstention from physical exercise, alcohol, soft drinks and caffeine, (b) fasting for at least 8 h, (c) an acclimation period of 10 min, and (d) 60 min assessment in a supine position. Resting $ \dot{V}{\text{O}}_{2} $ significantly changed during the 60 min (F = 37.4, P < 0.001), exhibiting a monoexponential decrease before reaching an asymptote. Post hoc pairwise comparisons showed that significant differences existed between consecutive means until the 30 min time point, after which there were no significant differences. The $ \dot{V}{\text{O}}_{2} $ response across trials exhibited high test–retest reliability, with within-subject coefficients of variations at each time point ranging from 2.8 to 7.0 % and intraclass correlation coefficients ranging from 0.90 to 0.99. The reliability was higher from the 25 min time point onwards. Based on these findings, the following recommendations are made to promote accurate assessment of resting $ \dot{V}{\text{O}}_{2} $ : (a) initiate the resting $ \dot{V}{\text{O}}_{2} $ measurement with 10 min of acclimation to the assessment apparatus, (b) determine resting $ \dot{V}{\text{O}}_{2} $ for a minimum of 30 min, until an apparent $ \dot{V}{\text{O}}_{2} $ steady state has been achieved; and (c) determine resting $ \dot{V}{\text{O}}_{2} $ for a further 5 min, with the average of this last 5 min of data being regarding as the resting $ \dot{V}{\text{O}}_{2} $ .     

\dot{V}_{{{\text{O}}_{2} { \max }}} is not altered by self-pacing during incremental exercise

We tested the hypothesis that incremental cycling to exhaustion that is paced using clamps of the rating of perceived exertion (RPE) elicits higher $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ values compared to a conventional ramp incremental protocol when test duration is matched. Seven males completed three incremental tests to exhaustion to measure $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ . The incremental protocols were of similar duration and included: a ramp test at 30 W min^?1 with constant cadence (RAMP1); a ramp test at 30 W min^?1 with cadence free to fluctuate according to subject preference (RAMP2); and a self-paced incremental test in which the power output was selected by the subject according to prescribed increments in RPE (SPT). The subjects also completed a $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ ‘verification’ test at a fixed high-intensity power output and a 3-min all-out test. No difference was found for $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ between the incremental protocols (RAMP1 = 4.33 ± 0.60 L min^?1; RAMP2 = 4.31 ± 0.62 L min^?1; SPT = 4.36 ± 0.59 L min^?1; P > 0.05) nor between the incremental protocols and the peak $ \dot{V}_{{{\text{O}}_{2} }} $ measured during the 3-min all-out test (4.33 ± 0.68 L min^?1) or the $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ measured in the verification test (4.32 ± 0.69 L min^?1). The integrated electromyogram, blood lactate concentration, heart rate and minute ventilation at exhaustion were not different (P > 0.05) between the incremental protocols. In conclusion, when test duration is matched, SPT does not elicit a higher $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ compared to conventional incremental protocols. The striking similarity of $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ measured across an array of exercise protocols indicates that there are physiological limits to the attainment of $ \dot{V}_{{{\text{O}}_{2} { \max }}} $ that cannot be exceeded by self-pacing.     

Exponential protocols for cardiopulmonary exercise testing on treadmill and cycle ergometer

An extended exponential exercise protocol was validated by comparing submaximal and maximal parameters with those obtained by linear protocol. Normal subjects (n = 16, 20–69 years) undertook maximal exercise tests on treadmill and cycle ergometer. The subjects had a wide range of exercise capacity, and all were accommodated by the protocol. Mean oxygen uptake $ (\dot{V}_{{{\text{O}}_{ 2} }} ) $ agreed between protocols at gas exchange anaerobic threshold (θ) (95% CI of difference ?0.1 to +0.06 l min^?1) and at peak (95% CI of difference ?0.1 to +0.1 l min^?1). Mean $ {\hbox{pre-}}\theta \Updelta \dot{V}_{{{\text{O}}_{2} }} /\Updelta {\text{work rate}}(\dot{W}) $ slope on the cycle ergometer agreed between protocols (95% CI of the difference ?0.9 to +0.25 ml min^?1 W^?1). $ {\hbox{Post-}}\theta \Updelta \dot{V}_{{{\text{O}}_{2} }} /\Updelta \dot{W} $ slope was steeper than pre-θ, and steeper by linear than by exponential protocol (P = 0.0001). It is concluded that the exponential protocol is valid for the measurement of submaximal and maximal exercise parameters in subjects with a wide range of exercise capacity.     

Prediction of peak oxygen uptake from differentiated ratings of perceived exertion during wheelchair propulsion in trained wheelchair sportspersons

Purpose

To assess the validity of predicting peak oxygen uptake ( $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ ) from differentiated ratings of perceived exertion (RPE) obtained during submaximal wheelchair propulsion.

Methods

Three subgroups of elite male wheelchair athletes [nine tetraplegics (TETRA), nine paraplegics (PARA), eight athletes without spinal cord injury (NON-SCI)] performed an incremental speed exercise test followed by graded exercise to exhaustion ( $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ test). Oxygen uptake ( $ {\dot{\text{V}}}{\text{O}}_2$ ), heart rate (HR) and differentiated RPE (Central RPE_C, Peripheral RPE_P and Overall RPE_O) were obtained for each stage. The regression lines for the perceptual ranges 9–15 on the Borg 6–20 scale ratings were performed to predict $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ .

Results

There were no significant within-group mean differences between measured $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ (mean 1.50 ± 0.39, 2.74 ± 0.48, 3.75 ± 0.33 L min^?1 for TETRA, PARA and NON-SCI, respectively) and predicted $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ determined using HR or differentiated RPEs for any group (P > 0.05). However, the coefficients of variation (CV %) between measured and predicted $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ using HR showed high variability for all groups (14.3, 15.9 and 9.7 %, respectively). The typical error ranged from 0.14 to 0.68 L min^?1 and the CV % between measured and predicted $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ using differentiated RPE was ≤11.1 % for TETRA, ≤7.5 % for PARA and ≤20.2 % for NON-SCI.

Conclusions

Results suggest that differentiated RPE may be used cautiously for TETRA and PARA athletes when predicting $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ across the perceptual range of 9–15. However, predicting $ {\dot{\text{V}}}{\text{O}}_{{\text{2peak}}}$ is not recommended for the NON-SCI athletes due to the large CV %s (16.8, 20.2 and 18.0 %; RPE_C, RPE_P and RPE_O, respectively).     

Influence of exercise intensity on respiratory muscle fatigue and brachial artery blood flow during cycling exercise

Purpose

During high intensity exercise, both respiratory muscle fatigue and cardiovascular reflexes occur; however, it is not known how inactive limb blood flow is influenced. The purpose of this study was to determine the influence of moderate and high exercise intensity on respiratory muscle fatigue and inactive limb muscle and cutaneous blood flow during exercise.

Methods

Twelve men cycled at 70 and 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) for 20 min. Subjects also performed a second 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) test after ingesting 1,800 mg of N-acetylcysteine (NAC), which has been shown to reduce respiratory muscle fatigue (RMF). Maximum inspiratory pressures (P _Imax), brachial artery blood flow (BABF), cutaneous vascular conductance (CVC), and mean arterial pressure were measured at rest and during exercise.

Results

Significant RMF occurred with 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) (P _Imax, ?12.8 ± 9.8 %), but not with 70 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) (P _Imax, ?5.0 ± 5.9 %). BABF and BA vascular conductance were significantly lower at end exercise of the 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) test compared to the 70 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) test. CVC during exercise was not different (p > 0.05) between trials. With NAC, RMF was reduced (p < 0.05) and BABF was significantly higher (~30 %) compared to 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) (p < 0.05).

Conclusions

These data suggest that heavy whole-body exercise at 85 % \(\dot{V}{\text{O}}_{{ 2_{ {\rm max} } }}\) leads to RMF, decreases in inactive arm blood flow, and vascular conductance, but not cutaneous blood flow.     

Central leptin replacement enhances chemorespiratory responses in leptin-deficient mice independent of changes in body weight

Previous studies showed that leptin-deficient (ob/ob) mice develop obesity and impaired ventilatory responses to CO₂ $ \left( {{{\dot{V}}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}}} \right) $ . In this study, we examined if leptin replacement improves chemorespiratory responses to hypercapnia (7?% CO₂) in ob/ob mice and if these effects were due to changes in body weight or to the direct effects of leptin in the central nervous system (CNS). $ {\dot{V}_{{{\text{E}}\,}}}{\text{ - C}}{{\text{O}}_{{2}}} $ was measured via plethysmography in obese leptin-deficient- (ob/ob) and wild-type- (WT) mice before and after leptin (10???g/2???l?day) or vehicle (phosphate buffer solution) were microinjected into the fourth ventricle for four consecutive days. Although baseline $ {\dot{V}_{\text{E}}} $ was similar between groups, obese ob/ob mice exhibited attenuated $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ compared to WT mice (134?±?9 versus 196?±?10?ml?min^?1). Fourth ventricle leptin treatment in obese ob/ob mice significantly improved $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ (from 131 ± 15 to 197 ± 10?ml?min^?1) by increasing tidal volume (from 0.38?±?0.03 to 0.55?±?0.02?ml, vehicle and leptin, respectively). Subcutaneous leptin administration at the same dose administered centrally did not change $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ in ob/ob mice. Central leptin treatment in WT had no effect on $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ . Since the fourth ventricle leptin treatment decreased body weight in ob/ob mice, we also examined $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ in lean pair-weighted ob/ob mice and found it to be impaired compared to WT mice. Thus, leptin deficiency, rather than obesity, is the main cause of impaired $ {\dot{V}_{{{\text{E}}\,}}}{ - }\,{\text{C}}{{\text{O}}_{{2}}} $ in ob/ob mice and leptin appears to play an important role in regulating chemorespiratory response by its direct actions on the CNS.     

Cycling time to failure is better maintained by cold than contrast or thermoneutral lower-body water immersion in normothermia

Purpose

To examine the effects of four commonly used recovery treatments applied between two bouts of intense endurance cycling on the performance of the second bout in normothermia (~21 °C).

Methods

Nine trained men completed two submaximal exhaustive cycling bouts (Ex1 and Ex2: 5 min at ~50 % ${\dot{\text{V}}\text{O}}_{2}$ peak, followed by 5 min at ~60 % ${\dot{\text{V}}\text{O}}_{2}$ peak and then ~80 % ${\dot{\text{V}}\text{O}}_{2}$ peak to failure) separated by 30 min of (a) cold water immersion at 15 °C (C15), (b) contrast water therapy alternating 2.5 min at 8 °C and 2.5 min at 40 °C (CT), (c) thermoneutral water immersion at 34 °C (T34) and (d) cycling at ~40 % ${\dot{\text{V}}\text{O}}_{2}$ peak (AR).

Results

Exercise performance, cardiovascular and metabolic responses during Ex1 were similar among all trials. However, time to failure (~80 % ${\dot{\text{V}}\text{O}}_{2}$ peak bout) during Ex2 was significantly (P < 0.05) longer in C15 (18.0 ± 1.6) than in CT (14.5 ± 1.5), T34 (12.4 ± 1.4) and AR (10.6 ± 1.0); and it was also longer (P < 0.05) in CT than AR. Core temperature and heart rate were significantly (P < 0.05) lower during the initial ~15 min of Ex2 during C15 compared with all other conditions but they reached similar levels at the end of Ex2.

Conclusions

A 30 min period of C15 was more beneficial in maintaining intense submaximal cycling performance than CT, T34 and AR; and CT was also more beneficial than T34 and AR. These effects were not mediated by the effect of water immersion per se, but by the continuous (C15) or intermittent (CT) temperature stimulus (cold) applied throughout the recovery.     

One night of sleep deprivation decreases treadmill endurance performance

The aim was to test the hypothesis that one night of sleep deprivation will impair pre-loaded 30 min endurance performance and alter the cardio-respiratory, thermoregulatory and perceptual responses to exercise. Eleven males completed two randomised trials separated by 7 days: once after normal sleep (496 (18) min: CON) and once following 30 h without sleep (SDEP). After 30 h participants performed a 30 min pre-load at 60% $ \dot{V}{\text{O}}_{2\max } $ followed by a 30 min self-paced treadmill distance test. Speed, RPE, core temperature (T _re), mean skin temperature (T _sk), heart rate (HR) and respiratory parameters ( $ \dot{V}{\text{O}}_{2} $ , $ \dot{V}{\text{CO}}_{2} $ , $ \dot{V}{\text{E}} $ , RER pre-load only) were measured. Less distance (P = 0.016, d = 0.23) was covered in the distance test after SDEP (6037 (759) 95%CI 5527 to 6547 m) compared with CON (6224 (818) 95%CI 5674 to 6773 m). SDEP did not significantly alter T _re at rest or thermoregulatory responses during the pre-load including heat storage (0.8°C) and T _sk. With the exception of raised $ \dot{V}{\text{O}}_{2} $ at 30 min on the pre-load, cardio-respiratory parameters, RPE and speed were not different between trials during the pre-load or distance test (distance test mean HR, CON 174 (12), SDEP 170 (13) beats min^?1: mean RPE, CON 14.8 (2.7), SDEP 14.9 (2.6)). In conclusion, one night of sleep deprivation decreased endurance performance with limited effect on pacing, cardio-respiratory or thermoregulatory function. Despite running less distance after sleep deprivation compared with control, participants’ perception of effort was similar indicating that altered perception of effort may account for decreased endurance performance after a night without sleep.     

Adaptations in muscle metabolic regulation require only a small dose of aerobic-based exercise

This study investigated the hypothesis that the duration of aerobic-based cycle exercise would affect the adaptations in substrate and metabolic regulation that occur in vastus lateralis in response to a short-term (10 day) training program. Healthy active but untrained males (n = 7) with a peak aerobic power ( $ \dot{V}{\text{O}}_{{ 2 {\text{ peak}}}} $ ) of 44.4 ± 1.4 ml kg^?1 min^?1 participated in two different training programs with order randomly assigned (separated by ≥2 weeks). The training programs included exercising at a single intensity designated as light (L) corresponding to 60 % $ \dot{V}{\text{O}}_{{ 2 {\text{ peak}}}} $ , for either 30 or 60 min. In response to a standardized task (60 % $ \dot{V}{\text{O}}_{{ 2 {\text{ peak}}}} $ ), administered prior to and following each training program, L attenuated the decrease (P < 0.05) in phosphocreatine and the increase (P < 0.05) in free adenosine diphosphate and free adenosine monophosphate but not lactate. These effects were not altered by daily training duration. In the case of muscle glycogen, training for 60 versus 30 min exaggerated the increase (P < 0.05) that occurred, an effect that extended to both rest and exercise concentrations. No changes were observed in $ \dot{V}{\text{O}}_{{ 2 {\text{ peak}}}} $ measured during progressive exercise to fatigue or in $ \dot{V}{\text{O}}_{ 2} $ and RER during submaximal exercise with either training duration. These findings indicate that reductions in metabolic strain, as indicated by a more protected phosphorylation potential, and higher glycogen reserves, can be induced with a training stimulus of light intensity applied for as little as 30 min over 10 days. Our results also indicate that doubling the duration of daily exercise at L although inducing increased muscle glycogen reserves did not result in a greater metabolic adaptation.     

The verification phase and reliability of physiological parameters in peak testing of elite wheelchair athletes

The purpose of this study was (1) to examine the value of a verification phase (VER) in a peak testing protocol and (2) to assess the reliability of peak physiological variables in wheelchair athletes. On two separate days, eight tetraplegic (TETRA), eight paraplegic (PARA) and eight non-spinal cord-injured (NON-SCI) athletes performed treadmill ergometry, consisting of a graded exercise test to exhaustion (GXT) followed by a VER. Peak oxygen uptake $ \left( {\dot{V}{\text{O}}_{{ 2 {\text{peak}}}} } \right) $ was compared (1) between GXT and VER and (2) between test days. $ \dot{V}{\text{O}}_{{2{\text{peak}}}} $ did not differ between GXT and VER (P = 0.27), and coefficients of variation between GXT and VER were in the range of 2.9 and 6.4 % for all subgroups. Coefficients of variation of $ \dot{V}{\text{O}}_{{2{\text{peak}}}} $ between test days were 9.3 % (TETRA), 4.5 % (PARA) and 3.3 % (NON-SCI). It is therefore concluded that whilst a VER can be used for a more robust determination of $ \dot{V}{\text{O}}_{{2{\text{peak}}}} $ , a deviation of up to ~6 % between GXT and VER should be considered as acceptable. For between-day analyses, relatively large changes in $ \dot{V}{\text{O}}_{{2{\text{peak}}}} $ are required to confirm “true” differences, especially in TETRA athletes. This may be due to their lower aerobic capacity, which results in a larger relative variation compared with the other subgroups.     

Exercise-induced muscle damage from bench press exercise impairs arm cranking endurance performance

The effects of exercise-induced muscle damage (EIMD) on the physiological, metabolic and perceptual responses during upper body arm cranking exercise are unknown. Nine physically active male participants performed 6 min of arm cranking exercise at ventilatory threshold (VT), followed by a time to exhaustion (TTE) trial at a workload corresponding to 80 % of the difference between VT and $ \dot V{\text{O}}_ {2{\rm peak}} $ 48 h after bench pressing exercise (10 × 6 repetitions at 70 % one repetition maximum) or 20 min sitting (control). Reductions in isokinetic strength and increased muscle soreness of the elbow flexors and extensors were evident at 24 and 48 h after bench pressing exercise (P < 0.05). Despite no change in $ \dot V{\text{O}}_2 $ , $ \dot V_{\text{E}} $ , HR and blood lactate concentration ([Bla]) between conditions (P > 0.05), rating of perceived exertion (RPE) was higher during the 6 min arm cranking after bench pressing exercise compared to the control condition (P < 0.05). TTE was reduced in the treatment condition (207.2 ± 91.9 cf. 293.4 ± 75.6 s; P < 0.05), as were end $ \dot V{\text{O}}_2 $ (P < 0.05) and [Bla] at 0, 5 and 10 min after exercise (P < 0.05). RPE during the TTE trial was higher after bench pressing (P < 0.05), although end RPE was not different between conditions (P > 0.05). This study provides evidence that EIMD caused by bench pressing exercise increases the sense of effort during arm cranking exercise that leads to a reduced exercise tolerance. The findings have implications for individuals participating in concurrent endurance and resistance training of the upper body.     

Differences in exercise limb blood flow and muscle deoxygenation with age: contributions to O2 uptake kinetics

The adjustments of pulmonary oxygen uptake $ \left( {\mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} } \right), $ limb blood flow (LBF) and muscle deoxygenation (ΔHHb) were examined during transitions to moderate-intensity, knee-extension exercise in seven older (OA; 71 ± 7 year) and seven young (YA; 26 ± 3 year) men. YA and OA performed repeated step transitions from an active baseline (3 W; 100 g) to a similar relative intensity of ~80% estimated lactate threshold (θ_L), and YA also performed the same absolute work rate as the OA (24 W, 800 g). Breath-by-breath $ \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} , $ femoral artery LBF (Doppler ultrasound) and muscle HHb (near-infrared spectroscopy) were measured. Phase 2 $ \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} , $ LBF, and ΔHHb data were fit with a mono-exponential model. $ \tau \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} $ was greater in OA (58 ± 21 s) than YA_80% (31 ± 9 s) and YA_24W (29 ± 11 s). The increase in LBF per increase in $ \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} $ was not different between groups (5.3–5.8 L min^?1/L min^?1); however, the τLBF was greater in OA (44 ± 19 s) than YA_24W (18 ± 7 s). The overall adjustment in ΔHHb (τ′ΔHHb) was not different between OA and YA, but was faster than $ \tau \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} $ in OA. This faster τ′ΔHHb than $ \tau \mathop {{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} $ resulted in an “overshoot” of the normalized $ \Updelta {\text{HHb}}/\Updelta\mathop{{V}}\limits^{ \cdot } {\text{O}}_{{2\,{\text{p}}}} $ response relative to the steady state level that was significantly greater in OA compared with YA suggesting that the adjustment of microvascular blood flow is slowed in OA thereby requiring a greater reliance on O₂ extraction during the transition to exercise.     

Acute supra-therapeutic oral terbutaline administration has no ergogenic effect in non-asthmatic athletes

This study aimed to investigate the effects on a possible improvement in aerobic and anaerobic performance of oral terbutaline (TER) at a supra-therapeutic dose in 7 healthy competitive male athletes. On day 1, ventilatory threshold, maximum oxygen uptake $ (\dot{V}O_{2\max }) $ and corresponding power output were measured and used to determine the exercise load on days 2 and 3. On days 2 and 3, 8 mg of TER or placebo were orally administered in a double-blind process to athletes who rested for 3 h, and then performed a battery of tests including a force–velocity exercise test, running sprint and a maximal endurance cycling test at Δ50 % (50 % between VT and $ \dot{V}{\text{O}}_{2\max } $ ). Lactatemia, anaerobic parameters and endurance performance ( $ \dot{V}{\text{O}}_{ 2} ,\dot{V}E $ and time until exhaustion) were raised during the corresponding tests. We found that TER administration did not improve any of the parameters of aerobic performance (p > 0.05). In addition, no change in $ \dot{V}{\text{O}}_{2} $ kinetic parameters was found with TER compared to placebo (p > 0.05). Moreover, no enhancement of the force–velocity relationship was observed during sprint exercises after TER intake (p > 0.05) and, on the contrary, maximal strength decreased significantly after TER intake (p < 0.05) but maximal power remained unchanged (p > 0.05). In conclusion, oral acute administration of TER at a supra-therapeutic dose seems to be without any relevant ergogenic effect on anaerobic and aerobic performances in healthy athletes. However, all participants experienced adverse side effects such as tremors.     

Energy cost of arm stroke,leg kick,and the whole stroke in competitive swimming styles

In male elite swimmers \(\dot V_{{\text{O}}_{\text{2}} } \) at a given velocity in freestyle and backstroke was on average 1 to 2 l x min^?1 lower as compared with breaststroke and butterfly. Except for breaststroke, swimming with arm strokes only demanded a lower \(\dot V_{{\text{O}}_{\text{2}} } \) at a given submaximal velocity than the whole stroke. In freestyle and backstroke the submaximal \(\dot V_{{\text{O}}_{\text{2}} } \) of leg kick at a given velocity was clearly higher than the whole stroke. The highest velocity during maximal swimming was always attained with the whole stroke, and the lowest with the leg kick, except for breast stroke, where the leg kick was most powerful. At a given submaximal \(\dot V_{{\text{O}}_{\text{2}} } \) , heart rate and \(\dot V_{\text{E}} :\dot V_{{\text{O}}_{\text{2}} } \) tended to be higher during swimming with arm strokes only as compared with the whole stroke. Highest values for \(\dot V_{{\text{O}}_{\text{2}} } \) , heart rate and blood lactate during maximal exercise were almost always attained when swimming the whole stroke, and lowest when swimming with arm strokes only. At higher velocities body drag was 0.5 to 0.9 kp lower when arms or legs were supported by a cork plate as compared with body drag without support.