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Biomechanics and Medicine in Swimming XI

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Oxygen Uptake K<strong>in</strong>etics Around the Respiratory<br />

Compensation Po<strong>in</strong>t <strong>in</strong> Swimm<strong>in</strong>g<br />

chaPter3.PhysioLogy<strong>and</strong>Bioenergetics<br />

study was to describe VO2 k<strong>in</strong>etics throughout the heavy <strong>and</strong> severe<br />

exercise doma<strong>in</strong>s dur<strong>in</strong>g front-crawl swimm<strong>in</strong>g, consider<strong>in</strong>g RCP as the<br />

transition parameter between them.<br />

Pessôa Filho, d.M.<br />

215<br />

1 , reis, J.F. 2 , Alves, F.B. 2 , denadai, B.s. 1<br />

1Paulista State University, Brazil<br />

2Faculty of Human K<strong>in</strong>etics, Technical University of Lisbon, Portugal<br />

The purpose of this study was to describe VO2 k<strong>in</strong>etics throughout the<br />

heavy <strong>and</strong> severe doma<strong>in</strong>s dur<strong>in</strong>g swimm<strong>in</strong>g. N<strong>in</strong>e swimmers completed<br />

two swimm<strong>in</strong>g tests to measure the condition<strong>in</strong>g <strong>in</strong>dexes (ventilatory<br />

threshold (VT), respiratory compensation po<strong>in</strong>t (RCP), <strong>and</strong> VO2max )<br />

<strong>and</strong> VO2 k<strong>in</strong>etics (two trials <strong>in</strong>tensities set at 2.5% below <strong>and</strong> above the<br />

crawl velocity at RCP, last<strong>in</strong>g 420s). In both cases, a portable breathby-breath<br />

system connected to a respiratory snorkel <strong>and</strong> valve was used.<br />

The trial below RCP elicited only a sub-maximal rate (91.6±5.7%VO-<br />

2max ), with a slow component of 391ml·m<strong>in</strong>-1 beg<strong>in</strong>n<strong>in</strong>g after 154s. The<br />

trial above RCP showed a time delay of 188s for the slow component<br />

(399ml·m<strong>in</strong>-1 Method<br />

Subjects: N<strong>in</strong>e well-tra<strong>in</strong>ed male swimmers (21.0 ± 7.2 yr, 68.6 ± 9.2 kg,<br />

178.2 ± 6.4 cm, 13.2 ± 4.1% body fat, <strong>and</strong> ~4.0 ± 0.7 L.m<strong>in</strong><br />

), elicit<strong>in</strong>g a rate of 104.6±9.5%VO2max . Thus, expected<br />

VO2 k<strong>in</strong>etics for heavy <strong>and</strong> severe doma<strong>in</strong>s was characterized<br />

around RCP.<br />

Key-word: Vo2 k<strong>in</strong>etics, heavy <strong>and</strong> severe doma<strong>in</strong>s, respiratory compensation<br />

po<strong>in</strong>t<br />

IntroductIon<br />

The boundary between heavy <strong>and</strong> severe exercise denotes a considerable<br />

change <strong>in</strong> exercise tolerance. Accord<strong>in</strong>g to Jones & Poole (2005), the<br />

upper boundary for the heavy doma<strong>in</strong> is def<strong>in</strong>ed as the highest exercise<br />

<strong>in</strong>tensity <strong>in</strong> which oxygen uptake (VO2 ) <strong>and</strong> blood lactate concentration<br />

([lactate]) can be ma<strong>in</strong>ta<strong>in</strong>ed at an elevated but steady-state level.<br />

By def<strong>in</strong>ition, both critical power (CP: the asymptote of the power (P)<br />

–time (t) relationship, represents the limit<strong>in</strong>g parameter to the aerobic<br />

supply, compris<strong>in</strong>g the notion that if P ≤ CP, the anaerobic supply is<br />

never required, <strong>and</strong> endurance time is <strong>in</strong>f<strong>in</strong>itely long – Morton, 2006)<br />

<strong>and</strong> maximal lactate steady-state (MLSS: highest constant workload<br />

that can be ma<strong>in</strong>ta<strong>in</strong>ed over time without cont<strong>in</strong>uous blood lactate accumulation<br />

– Beneke, 2003) match the physiological responses encompassed<br />

<strong>in</strong> the upper boundary of the heavy doma<strong>in</strong>.<br />

However, CP <strong>in</strong>tensity cannot be ma<strong>in</strong>ta<strong>in</strong>ed without a substantial<br />

<strong>in</strong>crease <strong>in</strong> blood lactate concentration, <strong>and</strong> other physiological parameters<br />

(Pr<strong>in</strong>gle & Jones, 2002; Dekerle et al., 2003). Comparisons between<br />

the CP <strong>and</strong> power associated to MLSS suggest that both are different<br />

<strong>and</strong> should not be used <strong>in</strong>terchangeably (Pr<strong>in</strong>gle & Jones, 2002). Moreover,<br />

the critical swimm<strong>in</strong>g velocity (CV), correspond<strong>in</strong>g to the slope<br />

of the distance–time relationship (Sd–t), lies with<strong>in</strong> the severe <strong>in</strong>tensity<br />

doma<strong>in</strong> with the physiological responses characteriz<strong>in</strong>g the heavy <strong>and</strong><br />

severe <strong>in</strong>tensity doma<strong>in</strong>s when swimm<strong>in</strong>g 5% slower <strong>and</strong> 5% faster than<br />

Sd-t, respectively (Dekerle et al., 2009). The dependence of the P-t relationship<br />

on the choice of predictive trials may expla<strong>in</strong> the mis<strong>in</strong>terpretation<br />

of its mathematical def<strong>in</strong>ition as the highest work rate that can be<br />

ma<strong>in</strong>ta<strong>in</strong>ed for a very long time without fatigue (Dekerle et al., 2009).<br />

Exercis<strong>in</strong>g at 50% of the difference between the mode-specific LT<br />

<strong>and</strong> VO2max (50%ΔVO2) is an alternative <strong>in</strong>dex to the transition between<br />

heavy <strong>and</strong> severe doma<strong>in</strong>s ( Jones & Poole, 2005). Surpris<strong>in</strong>gly,<br />

whereas the LT has been estimated from gas-exchange responses as<br />

ventilatory threshold (VT: ris<strong>in</strong>g <strong>in</strong> the VE/VO2 curve with no change<br />

<strong>in</strong> the VE/VCO2 curve – Beaver et al., 1986), the respiratory compensation<br />

po<strong>in</strong>t (RCP: po<strong>in</strong>t <strong>in</strong> the plot of VE vs. VCO2 where VE rises<br />

more rapidly <strong>in</strong> a phase of relative hyperventilation - Beaver et al., 1986)<br />

for metabolic acidosis <strong>and</strong> buffer<strong>in</strong>g events <strong>in</strong> the tissues, has not clearly<br />

demarcated the upper boundary of the heavy doma<strong>in</strong>. Although no significant<br />

differences were obta<strong>in</strong>ed between VO2 <strong>and</strong> power output at<br />

CP <strong>and</strong> RCP <strong>in</strong> cycl<strong>in</strong>g (Dekerle et al., 2003). Thus, the purpose of this<br />

-1 VO2max )<br />

participated of this study. All subjects were advised to tests protocols<br />

<strong>and</strong> gave written consent. This research was approved by the local Ethics<br />

Committee.<br />

Experimental design: The subjects were required to perform three<br />

stages of experimentation. The first stage <strong>in</strong>volved the determ<strong>in</strong>ation<br />

of VT, RCP <strong>and</strong> VO2max . The second stage <strong>in</strong>volved two swimm<strong>in</strong>g<br />

sessions with the subjects perform<strong>in</strong>g two repetitions of square-wave<br />

transitions, from rest to one of two exercise <strong>in</strong>tensities set at 2.5% below<br />

(v-2.5% ) <strong>and</strong> above (v +2.5% ) the velocity at RCP, correspond<strong>in</strong>g to 36.3 ±<br />

7.0% <strong>and</strong> 74.1 ± 11.4% of the delta between velocity at VT <strong>and</strong> VO2max .<br />

No more than two transitions were completed <strong>in</strong> one day, with at least<br />

1h of recovery between transitions. All the procedures were not extended<br />

beyond 3–4 weeks for each subject, <strong>and</strong> the study was completed <strong>in</strong><br />

about eight weeks. All tests were performed <strong>in</strong> a 50-m <strong>in</strong>door swimm<strong>in</strong>g<br />

pool. Dur<strong>in</strong>g the exercise tests, pulmonary gas exchange was determ<strong>in</strong>ed<br />

breath-by-breath with a portable automated system (K4b2, Cosmed),<br />

which was calibrated before each test, <strong>and</strong> connected to the swimmer<br />

by a special respiratory snorkel <strong>and</strong> valve system, previously validated by<br />

Kesk<strong>in</strong>en et al. (2002).<br />

Incremental protocol: Subjects performed an <strong>in</strong>termittent <strong>in</strong>cremental<br />

test (300-m stages) to exhaustion. The velocity <strong>in</strong>crements were del<strong>in</strong>eated<br />

to four or five percentages designed to atta<strong>in</strong> the 400-m maximal swimm<strong>in</strong>g<br />

velocity at the last stage. The breath-by-breath VO2 responses were<br />

smoothed <strong>and</strong> averaged every 30s. VO2max was calculated as the highest<br />

30s value achieved dur<strong>in</strong>g the <strong>in</strong>cremental test. The swimm<strong>in</strong>g velocity<br />

related to the VO2max (vVO2max ) was def<strong>in</strong>ed as the lowest velocity that<br />

elicited VO2max (Demarie et al. 2001). The lower <strong>and</strong> upper boundary for<br />

heavy <strong>in</strong>tensity doma<strong>in</strong>s were determ<strong>in</strong>ed from gas exchange responses at<br />

VT <strong>and</strong> RPC respectively, follow<strong>in</strong>g the recommendations of Beaver et<br />

al. (1986). VT was exam<strong>in</strong>ed visually us<strong>in</strong>g plots of VE /VCO2 , VE /VO2 ,<br />

end-tidal PCO2 (PETCO2 ) <strong>and</strong> end-tidal PO2 (PETO2 ). The criteria used<br />

for determ<strong>in</strong>ation of VT <strong>and</strong> RCP were a non-l<strong>in</strong>ear <strong>in</strong>crease <strong>in</strong> VE/VO2 <strong>and</strong> PETO2 curves without a correspond<strong>in</strong>g change <strong>in</strong> VE/VCO2 <strong>and</strong><br />

PETCO2 curves; <strong>and</strong> an <strong>in</strong>crease <strong>in</strong> both VE/VO2 <strong>and</strong> VE/VCO2 <strong>and</strong> a<br />

decrease <strong>in</strong> PETCO2 , respectively. VT <strong>and</strong> RCP location po<strong>in</strong>t were estimated<br />

by two <strong>in</strong>dependent observers. The highest 30-s average VO2 for<br />

these steps was considered the VO2 at VT <strong>and</strong> RCP.<br />

VO2 k<strong>in</strong>etic model<strong>in</strong>g: Subjects performed two repetitions of squarewave<br />

transitions of 7 m<strong>in</strong> duration at the two exercise <strong>in</strong>tensities on<br />

separate days. After a 3-4 m<strong>in</strong> warm-up at a low swimm<strong>in</strong>g velocity<br />

followed by 5 m<strong>in</strong> of rest, the subjects were <strong>in</strong>structed to perform the<br />

required <strong>in</strong>tensity. Intensities were set at 2.5% below <strong>and</strong> above the velocity<br />

at RCP, which corresponded to 1.35 ± 0.05 m·s-1 <strong>and</strong> 1.28 ± 0.05<br />

m·s-1 67<br />

<strong>in</strong>structed to perform the required <strong>in</strong>tensity. Intensities were set at 2.5% below <strong>and</strong><br />

, respectively. For each exercise transition, the breath-by-breath<br />

above the velocity at RCP, which corresponded to 1.35 ± 0.05 m·s<br />

data were <strong>in</strong>terpolated to give second-by-second values. For every each<br />

<strong>in</strong>tensity, the transitions were then synchronized with the start of exercise<br />

<strong>and</strong> averaged to enhance the underly<strong>in</strong>g response characteristics.<br />

Nonl<strong>in</strong>ear regression techniques were used to fit VO2 data after the onset<br />

of exercise with a bi-exponential model (Equation 1) that provided<br />

an estimate of the on-transients: amplitudes (A1 <strong>and</strong> A2 ), time delays<br />

(TD1 <strong>and</strong> TD2 ) <strong>and</strong> time constants (t1 <strong>and</strong> t2 ). The <strong>in</strong>itial cardiodynamic<br />

component was not considered by elim<strong>in</strong>at<strong>in</strong>g the first 20s of data after<br />

the onset of exercise. The basel<strong>in</strong>e VO2 was def<strong>in</strong>ed as the average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of each transition.<br />

(1)<br />

-1 <strong>and</strong> 1.28 ± 0.05<br />

m·s -1 , respectively. For each exercise transition, the breath-by-breath data were<br />

<strong>in</strong>terpolated to give second-by-second values. For every each <strong>in</strong>tensity, the transitions<br />

were then synchronized with the start of exercise <strong>and</strong> averaged to enhance the<br />

underly<strong>in</strong>g response characteristics. Nonl<strong>in</strong>ear regression techniques were used to fi<br />

VO2 data after the onset of exercise with a bi-exponential model (Equation 1) tha<br />

provided an estimate of the on-transients: amplitudes (A1 <strong>and</strong> A2), time delays (TD1 <strong>and</strong><br />

TD2) <strong>and</strong> time constants (t1 <strong>and</strong> t2). The <strong>in</strong>itial cardiodynamic component was no<br />

considered by elim<strong>in</strong>at<strong>in</strong>g the first 20s of data after the onset of exercise. The basel<strong>in</strong>e<br />

VO2 was def<strong>in</strong>ed as the average VO2 measured dur<strong>in</strong>g rest<strong>in</strong>g 30s before the start of<br />

each transition.<br />

⎛ −<br />

⎛ −<br />

⎡ −<br />

t TD1<br />

⎞ ⎤ ⎡ −<br />

t TD2<br />

⎞<br />

⎜ ⎟<br />

⎜ ⎟ ⎤<br />

⎝ τ1<br />

⎠<br />

⎝ τ 2 ⎠<br />

VO2 ( t)<br />

= VO2b<br />

+ A1<br />

⎢1<br />

− l ⎥ + A2<br />

⎢1<br />

− l ⎥<br />

⎣ ⎦ ⎣ ⎦<br />

(1)<br />

The physiologically relevant <strong>in</strong>crease <strong>in</strong> VO2 is the amplitude of phase I (A1’), or<br />

primary component, which was calculated from:<br />

⎛ ( )<br />

⎜<br />

⎛ −<br />

TD2−TD1<br />

⎟<br />

⎞<br />

'<br />

⎞<br />

⎝<br />

τ 1⎠<br />

A = ⎜ −<br />

⎟<br />

1 A1<br />

1 l<br />

⎝<br />

⎠<br />

(2)<br />

Because the asymptotic value (A2) may represent a higher value than that actually

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