Cardiac output during exercise in paraplegic subjects

Summary The purpose of this study was to measure the cardiac output using the CO₂ rebreathing method during submaximal and maximal arm cranking exercise in six male paraplegic subjects with a high level of spinal cord injury (HP). They were compared with eight able bodied subjects (AB) who were not trained in arm exercise. Maximal O₂ consumption ( O_2max) was lower in HP (1.1 1·min^–1, SD 0.1; 17.5 ml·min^–·kg, SD 4) than in AB (2.5 1·min^–1, SD 0.6; 36.7 ml·min^–1·kg, SD 10.7). Maximal cardiac output was similar in the groups (HP, 141·min^–1 SD 2.6; AB, 16.81·min^–1 SD 4). The same result was obtained for maximal heart rate (f _c,max (HP, 175 beats·min^–1, SD 18; AB, 187 beats·min^–, SD 16) and the maximal stroke volume (HP, 82 ml, SD 13; AB, 91 ml, SD 27). The slopes of the relationshipf _c/ O₂ were higher in HP than AB (P<0.025) but when expressed as a % O_2max there were no differences. The results suggests a major alteration of oxygen transport capacity to active muscle mass in paraplegics due to changes in vasomotor regulation below the level of the lesion.     

Influence of acute maximal exercise on lecithin: cholesterol acyltransferase activity in healthy adults of differing aerobic performance

Summary To document the possible influence of a single episode of maximal aerobic stress on the serum lecithin: cholesterol acyltransferase (LCAT) activity in subjects with differing histories of training, two groups of healthy male adults [controls (C),n = 18, 28.6 years, SD 5.2, 50.1 ml · kg^–1 · min^–1 maximal O₂ uptake (VO_2max), SD 5.3; endurance trained athletes (T),n = 18, 31.4 years, SD 8.8, 65.0 ml · kg^–1 · min^–1 VO_2max, SD 2.8] were examined in a maximal aerobic stress test. In addition to the routine assessment of lipid status, LCAT activity was measured immediately before and after exercise. At rest nearly identical LCAT activity values were found in both groups: C 64.4 nmol · ml^–1 · h^–1, SD 16.7 vs T 65.0 nmol · ml^–1 · h^–1, SD 20.9. The post-exercise LCAT values induced by the maximal stress test increased significantly to (C) 95.7 nmol · ml^–1 · h^–1, SD 23.5, +48.6%,P<0.001; (T) 83.5 nmol · ml^–1 · h^–1, SD 24.3, +29.1%,P<0.01. Neither the pre nor the post-exercise individual LCAT activity values showed any significant correlation to the corresponding data on physical performance.     

The influence of body position on maximal performance in cycling

Summary Six healthy male subjects performed a 3-min supramaximal test in four different cycling positions: two with different trunk angles and two with different saddle-tube angles. Maximal power output and maximal oxygen uptake (VO_2max) were measured. Maximal power output was significantly higher in a standard sitting (SS, 381 W, SD 49) upright position compared to all other positions: standard racing (SR, 364 W, SD 49), recumbent backwards (RB, 355 W, SD 44) and recumbent forwards (RF, 341 W, SD 54). Although VO_2max was also highest in SS (4.31 l · min^–1, SD 0.5) upright position, the differences in VO_2max were not significant (SR, 4.21 · min^–1, SD 0.53; RB, 4.17 l · min^–1, SD 0.58; RF, 4.11 l · min^–1, SD 0.66). It is concluded that (supra)maximal tests on a cycle ergometer should be performed in a sitting upright position and not in a racing position. In some cases when cycling on the road, higher speeds can be attained when sitting upright. This is especially true when cycling uphill when high power must be generated to overcome gravity but the road speed, and hence the power required to overcome air resistance, is relatively low.     

Neuromuscular characteristics and fatigue in endurance and sprint athletes during a new anaerobic power test

The purpose of this study was to investigate neuromuscular and energy performance characteristics of anaerobic power and capacity and the development of fatigue. Ten endurance and ten sprint athletes performed a new maximal anaerobic running power test (MARP), which consisted ofn x 20-s runs on a treadmill with 100-s recovery between the runs. Blood lactate concentration [la^–]_b was measured after each run to determine submaximal and maximal indices of anaerobic power (P _3mmol·1 ^–1,P_5mmol·1 ^–1,P_10mmol·1 ^–1andP _max) which was expressed as the oxygen demand of the runs according to the American College of Sports Medicine equation: the oxygen uptake (ml·kg^–1·min^–1)=0.2·velocity (m·min^–1) +0.9·slope of treadmill (frac)·velocity (m·min^–1)+3.5. The height of rise of the centre of gravity of the counter movement jumps before (CMJ_rest) and during (CMJ) the MARP test, as well as the time of force production (t _F) and electromyographic (EMG) activity of the leg muscles of CMJ performed after each run were used to describe the neuromuscular performance characteristics. The maximal oxygen uptake ( _max), anaerobic and aerobic thresholds were determined in the _max test, which consisted ofn x 3-min runs on the treadmill. In the MARP-testP _max did not differ significantly between the endurance [116 (SD 6) ml·kg^–1·min^–1] and sprint [120 (SD 4) ml·kg^–1·min^–1] groups, even though CMJ_rest and peak [la^–]_b were significantly higher and _max was significantly lower in the sprint group than in the endurance group and CMJ_rest height correlated withP _max (r=0.50,P<0.05). The endurance athletes had significantly higher mean values ofP _3mmol·1 ^–1andP _5mmol·1 ^–1[89 (SD 7) vs 76 (SD 8) ml·kg^–1·min^–,P<0.001 and 101 (SD 5) vs 90 (SD 8) ml·kg^–1·min^–1,P<0.01. Significant positive correlations were observed between theP _3mmol·l ^–1and _max, anaerobic and aerobic thresholds. In the sprint group CMJ and the averaged integrated iEMG decreased andt _F increased significantly during the MARP test, while no significant changes occurred in the endurance group. The present findings would suggest thatP _max reflected in the main the lactacid power and capacity and to a smaller extent alactacid power and capacity. The duration of the MARP test and the large number of CMJ may have induced considerable energy and neuromuscular fatigue in the sprint athletes preventing them from producing their highest alactacidP _max at the end of the MARP test. Due to lower submaximal [la^–]_b (anaerobic sprinting economy) the endurance athletes were able to reach almost the sameP _max as the sprint athletes.     

Maximal oxygen uptake,anaerobic threshold and running economy in women and men with similar performances level in marathons

Sex differences in running economy (gross oxygen cost of running, C_R), maximal oxygen uptake (VO_2max), anaerobic threshold (Th_an), percentage utilization of aerobic power (% VO_2max), and Th_an during running were investigated. There were six men and six women aged 20–30 years with a performance time of 2 h 40 min over the marathon distance. The VO_2max, Th_an, and CR were measured during controlled running on a treadmill at 1° and 3° gradient. From each subject's recorded time of running in the marathon, the average speed (v _M) was calculated and maintained during the treadmill running for 11 min. The VO_{2 max} was inversely related to body mass (m _b), there were no sex differences, and the mean values of the reduced exponent were 0.65 for women and 0.81 for men. These results indicate that for running the unit ml·kg^–0.75·min^–1 is convenient when comparing individuals with different m _b. The VO_2max was about 10% (23 ml·kg^–0.75·min^–1) higher in the men than in the women. The women had on the average 10–12 ml·kg^–0.75·min^–1 lower VO₂ than the men when running at comparable velocities. Disregarding sex, the mean value of C_R was 0.211 (SEM 0.005) ml·kg^–1·m^–1 (resting included), and was independent of treadmill speed. No sex differences in Th_an expressed as % VO_2max or percentage maximal heart rate were found, but Than expressed as VO₂ in ml·kg^–0.75·min^–1 was significantly higher in the men compared to the women. The percentage utilization of f _emax and concentration of blood lactate at v _M was higher for the female runners. The women ran 2 days more each week than the men over the first 4 months during the half year preceding the marathon race. It was concluded that the higher VO_2max and Th_an in the men was compensated for by more running, superior C_R, and a higher exercise intensity during the race in the performance-matched female marathon runners.     

Endurance training slows down the kinetics of heart rate increase in the transition from moderate to heavier submaximal exercise intensities

Summary To find out whether endurance training influences the kinetics of the increases in heart rate (f _c) during exercise driven by the sympathetic nervous system, the changes in the rate off _c adjustment to step increments in exercise intensities from 100 to 150 W were followed in seven healthy, previously sedentary men, subjected to 10-week training. The training programme consisted of 30-min cycle exercise at 50%–70% of maximal oxygen uptake ( O_2max) three times a week. Every week during the first 5 weeks of training, and then after the 10th week the subjects underwent the submaximal three-stage exercise test (50, 100 and 150 W) with continuousf _c recording. At the completion of the training programme, the subjects' O_2max had increased significantly(39.2 ml·min^–1·kg^–1, SD 4.7 vs 46 ml·min^–1·kg^–1, SD 5.6) and the steady-statef _c at rest and at all submaximal intensities were significantly reduced. The greatest decrease in steady-statef _c was found at 150 W (146 beats·min^–1, SD 10 vs 169 beats·min^–1, SD 9) but the difference between the steady-statef _c at 150 W and that at 100 W (f _c) did not decrease significantly (26 beats·min^–1, SD 7 vs 32 beats·min^–1, SD 6). The time constant () of thef _c increase from the steady-state at 100 W to steady-state at 150 W increased during training from 99.4 s, SD 6.6 to 123.7 s, SD 22.7 (P<0.01) and the acceleration index (A=0.63·f _c·^–1) decreased from 0.20 beats·min^–1·s^–1, SD 0.05 to 0.14 beats·min^–1·s^–1, SD 0.04 (P<0.02). The major part of the changes in and A occurred during the first 4 weeks of training. It was concluded that heart acceleration following incremental exercise intensities slowed down in the early phase of endurance training, most probably due to diminished sympathetic activation.     

Maximal heart rates and plasma lactate concentrations observed in middle-aged men and women during a maximal cycle ergometer test

Summary The purpose of this study was to investigate criteria for maximal effort in middle-aged men and women undertaking a maximal exercise test until they were exhausted if no measurements of oxygen uptake are made. A large group of 2164 men and 975 women, all active in sports and aged between 40 and 65 years, volunteered for a medical examination including a progressive exercise test to exhaustion on a cycle ergometer. In the 3rd min of recovery a venous blood sample was taken to determine the plasma lactate concentration ([la^–]_{p, 3min}). Lactate concentration and maximal heart rate (f _{c, max}) were lower in the women than in the men (P<0.001). Multiple regression analyses were performed to assess the contribution of sex to [la^–]_{p, 3 min}, independent of age and f _c max, It was found that [la^–]_{p,3 min} was about 2.5 mmol·l^–1 lower in women than in men of the same age and f _{c, max}. In our population 88% of the men and 85% of the women met a combination of the following f _{c, max} and [la^–]_{p, 3min} criteria: f _{c, max} equal to or greater than 220 minus age beats·min^–1 and/or [la^–]_{p, 3min} equal to or greater than 8 mmol·l^–1 in the men and f _{c, max} equal to or greater than 220 minus age beats·min^–1 and/or [la^–]_{p, 3min} equal to or greater than 5.5 mmol·1^–1 in the women.     

Pathways of phosphate transport in chick jejunum

The effect of vitamin D₃ on intestinal phosphate (P_i) absorption was studied in everted sacs prepared from jejunum of either vitamin D-deficient (–D) or vitamin D-replete (+D) chicks. Vitamin D₃ stimulates the maximal velocity (V _max) of a mucosal active P_i transport mechanism from 125 to 314 nmol·min^–1·g^–1 tissue.K _m of this process remains virtually unchanged (–D: 0.15 mmol·l^–1; + D: 0.18 mmol·l^–1).Active P_i entry into the epithelium depends on extracellular Na⁺. Reduction of buffer Na⁺ reducesV _max in the + D group to 182 nmol·min^–1·g^–1 tissue but has no significant effect in the –D animals (V _max=105 nmol·min^–1·g^–1 tissue). In this group, the predominant effect of Na⁺ substitution is a shift ofK _m to 1.13 mmol·l^–1, whileK _m in the +D group is changed only to 0.53 mmol·l^–1.Transeptithelial P_i transport in the + D group involves the mucosal phosphate pump and hence an intracellular pathway, proceeding at a rate of 48 nmol·min^–1·g^–1 tissue. This is in contrast to –D P_i transfer (8 nmol·l^–1·g^–1 tissue) which is by a diffusional, Na⁺-insensitive, and presumably paracellular pathway.Transepithelial calcium transport (–D: 3.3 nmol·min^–1·g^–1; + D: 7.6 nmol·min^–1·g^–1 tissue) does not require the presence of extracellular Na⁺ and apparently involves pathways different from those of the P_i absorptive system.Presented in part at the Annual Meeting of the Austrian Biochemical Society, Salzburg, September 1978     

Intravenous instrumentation alters the autonomic state in humans

Intravascular instrumentation may induce syncope or presyncope. It is not known whether asymptomatic subjects also have autonomic reactions, albeit concealed. We addressed this issue by studying 44 healthy young male subjects of various levels of fitness, ranging from inactivity to athletic [mean maximal oxygen uptake was 49.1 (SD 10.7) ml·kg^–1·min^–1, range 28.7–71.9 ml·kg^–1·min^–1]. The autonomic response to venous cannulation was quantified by measuring heart rate before cannulation (HR1), after cannulation (HR₂), and after complete pharmacological autonomic blockade (HR₀ = the intrinsic heart rate). The sympathovagal balance before and after cannulation was computed as HR₁/HR₀ and HR₂/HR₀, respectively. The group means of heart rate and sympathovagal balance decreased significantly (paired Student's t-test P <0.01) from 62.5 to 59.9 beats·min^–, and from 0.71 to 0.68, respectively. The maximal decrease in heart rate was 8.8 beats·min^–1, and in the sympathovagal balance was 0.11. Our study demonstrated that the asymptomatic subjects responded to intravenous instrumentation with a concealed autonomic reaction. Thus, from our findings it would seem that intravenous instrumentation interferes with measurements relating to autonomic nervous system activity.     

Reduced exercise hyperaemia in calf muscles working at high contraction frequencies

Summary The effects of muscle contraction frequency on blood flow to the calf muscle (Q _calf) were studied in six female subjects, who performed dynamic plantar flexions at frequencies of 20, 40, 60, 80 and 100 contractions · min^–1, in a supine position. TheQ _calf measured by a mercury-in-rubber strain gauge plethysmograph, increased as contraction frequency increased and reached a peak at 60–80 contractions · min^–1. After 100 plantar flexions at 60 contractions · min^–1, the meanQ _calf was 30.95 (SEM 4.52) ml · 100 ml^–1 · min^–1. At 100 contractions · min^–1, however, it decreased significantly compared with that at 60 contractions · min^–1 at a specified time (2 min or exhaustion) or after a fixed amount of work (100 contractions). The contraction frequency at whichQ _calf reached a peak depended on the duration of exercise. The heart rate showed its highest mean value at 60 contractions · min^–1 and decreased significantly at 100 contractions · min^–1. The mean blood pressure was lower at 100 contractions · min^–1 than at 60 contractions · min^–1. The relaxation period between contractions, measured by recording the electromyogram from the gastrocnemius muscles, shortened markedly as the frequency increased; the mean value at 100 contractions · min^–1 was 0.14 (SEM 0.02) s, which corresponded to 35.7% of the contraction time. This shortened relaxation period between contractions should have led to the inhibition of exercise hyperaemia at the higher contraction frequencies.     

Phosphorus-31 magnetic resonance spectroscopy of forearm flexor muscles in student rowers using an exercise protocol adjusted for differences in cross-sectional muscle area

Summary To assess exercise energy metabolism of forearm flexor muscles in rowers, six male student rowers and six control subjects matched for age and sex were studied using phosphorus-31 magnetic resonance spectroscopy (³¹P-MRS). Firstly, to adjust for the effect of differences in cross-sectional muscle area, the maximal cross-sectional area (CSA_max) of the forearm flexor muscles was estimated in each individual using magnetic resonance imaging. Multistage exercise was then carried out with an initial energy production of 1 J · cm^–2 CSA_max for 1 min and an increment of 1 J · cm^–2 CSA_max every minute to the point of muscle exhaustion. A series of measurements of³¹P-MRS were performed every minute. The CSA_max was significantly greater in the student rowers than in the control subjects [19.8 (SD 2.2) vs 17.1 (SD 1.2) cm²,P<0.05]. The absolute maximal exercise intensity (J · min^–1) was greater in the rowers than in the control subjects. However, the maximal exercise intensity per unit of muscle cross sectional area (J · min^–1 · cm^–2) was not significantly different between the two groups. During mild to moderate exercise intensities, a decrease in phosphocreatine and an increase in inorganic phosphate before the onset of acidosis were significantly less in the rowers, indicating a requirement of less adenosine 5-diphosphate to drive adenosine 5-triphosphate production. The onset of acidosis was also significantly delayed in the rowers. No difference was observed in forearm blood flow between the two groups at the same exercise intensity (J · min^–1 · cm^–2). These results demonstrated that the findings of the maintenance of a higher level of phosphocreatine and a lower level of inorganic phosphate with less acidosis observed in the rowers were the results of the intrinsic characteristics of energy metabolism of their muscles and that these characteristics were independent of their greater cross-sectional muscle area.     

Age predicts cardiovascular,but not thermoregulatory,responses to humid heat stress

Cross-section comparisons of the effect of age on physiological responses to heat stress have yielded conflicting results, in part because of the inability to separate chronological age from factors which change in concert with the biological aging process. The present study was designed to examine the relative influence of age on cardiovascular and thermoregulatory responses to low intensity cycle exercise (60 W for 1 h) in a warm humid environment (35°C, 80% relative humidity). Specifically, the relative importance of age compared to other individual characteristics [maximal oxygen uptake ( _max), physical activity level, anthropometry, and adiposity] was determined by multiple regression analysis in a heterogeneous sample of 56 subjects in which age (20–73 years) and _max (1.864–44 l · min^–1) were not interrelated. Dependent variables (with ranges) included final values of thermoregulatory responses [rectal temperature (T _re, 37.8–39.2°C), calculated heat storage (S, 3.4–8.1 J · g^–1), sweat loss (238–847 g · m^–2)] and cardiovascular responses [heart rate (HR, 94–176 beats min^–1), forearm blood flow (FBF, 5.3–31.3 ml · 100 ml^–1 · min^–1), mean arterial blood pressure (MAP, 68–122 mmHg), and forearm vascular conductance (FVC = FBF · MAP^–1, 0.06–0.44 ml · 100 ml^–1 · min^–1 · mmHg^–1). Age had no significant influence onT _re,S, or sweat loss, all of which were closely related to _max. On the other hand, HR, MAP, FBF, and FVC were related to both age and _max. Anthropometric variables and adiposity had secondary, but statistically significant, effects on MAP, FBF, FVC, and sweat loss. With respect to exercise in a warm humid environment, it was concluded that the effect of age on body temperature and sweating was negligible compared to effects related to _max, but that chronological age had an independent effect on cardiovascular effector responses.     

Effect of prior exercise at different pedalling frequencies on maximal power in humans

Summary The effect of prior submaximal exercise performed at two different pedalling frequencies, 60 and 120 rev · min^–1, on maximal short-term power output (STPO) was investigated in seven male subjects during cycling exercise on an isokinetic cycle ergometer. Exercise of 6-min duration at a power output equivalent to 92 (SD 5)% maximal oxygen uptake , whether performed at a pedalling frequency of 60 or 120 rev · min^–1, reduced maximal STPO generated at 120 rev · min^–1 to a much greater extent than maximal STPO at 60 rev · min^–1. After 6-min submaximal exercise at 60 rev · min^–1 mean reductions in maximal STPO measured at 120 and 60 rev · min^–1 were 27 (SD 11)% and 15 (SD 9)% respectively, and were not significantly different from the reductions after exercise at 120 rev · min^–1, 20 (SD 13)% and 5 (SD 9)%, respectively. In addition, we measured the effect of prior exercise performed at the same absolute external mechanical power output [236 (SD 30)W] with pedalling frequencies of 60 and 120 rev · min^–1, Although the external power output was the same, the leg forces required (absolute as well as expressed as a proportion of the maximal leg force available at the same velocity) were much higher in prior exercise performed at 60 rev · min^–1. Nevertheless, maximal STPO generated at 120 rev · min^–1 was reduced after exercise at 120 rev-min^–1 [20 (SD 13) %,P<0.05] whereas no significant reduction in maximal STPO was found after prior exercise at 60 rev · min^–1. The present findings would suggest that exercise performed at 92 (SD 5)% , whether at 60 or at 120 rev · min^–1, selectively fatigues the faster fatigue-sensitive fibres resulting in a greater reduction in maximal STPO generated at 120 compared to 60 rev · min^–1. The greater fatigue of maximal STPO generated at 120 rev · min^–1 due to exercise performed at a power output of 236 (SD 30)W at 120 rev · min^–1 compared to 60 rev · min^–1 would suggest a relatively greater contribution of fast fatigue-sensitive fibres when higher movement frequencies and hence different muscle shortening velocities are used at this submaximal exercise intensity.     

Changes in structure and function of the human left ventricle after acclimatization to high altitude

Summary To analyse the role of changes in structure and function of the left ventricle in determining cardiac function at rest and during exercise, several two-dimensional and Doppler echocardiographic measurements were performed on 11 healthy subjects immediately before an Himalayan expedition (Nun, 7135 m), during acclimatization (3 weeks) and 14 days after the return. At rest decreases were found in cardiac index (CI) (3.23 l · min^–1 · m^–2, SD 0.4 vs 3.82 l · min^–1 · m^–2, SD 0.58,P < 0.01), left ventricular mass (55.3 g · m^–2, SD 9.4 vs 65.2 g · m^–2, SD 13.5,P < 0.005) and left ventricular end-diastolic volume (LVEDV) (53.9 ml · m^–2, SD 6.9 vs 64.8 ml · m^–2, SD 9.1,P < 0.001) after acclimatization; by contrast the coefficient of peak arterial pressure to left ventricular end-systolic volume (PAP/ESV) (7.8, SD 1.6 vs 6.0, SD 1.8,P < 0.005) and mean wall stress [286 kdyn · cm^–2, SD 31 vs 250 kdy · cm^–2, SD 21 (2.86 N · cm^–2, SD 0.31 vs 2.50 N · cm^–2, SD 0.21),P < 0.005] increased. After return to sea level, low values of CI and mass persisted despite a return to normal of LVEDV and preload. A reduction of PAP/ESV was also observed. At peak exercise, PAP/ESV (8.7, SD 2.4 vs 12.8, SD 2.0,P < 0.0025), CI (9.8 l · min^–1 m^–2, SD 2.5 vs 11.61 · min^–1 · m^–2, SD 1.6,P < 0.05) and the ejection fraction (69%, SD 6 vs 76%, SD 4,P < 0.05) were lower after return to sea level than before departure. The depressed left ventricular performance after prolonged exposure to hypoxia may be related to changes in structure and function including reduction in preload, loss of myocardial mass and depression of inotropic state.     

Bio-energetic profile in 144 boys aged from 6 to 15 years with special reference to sexual maturation

Summary The effects of growth and pubertal development on bio-energetic characteristics were studied in boys aged 6–15 years (n = 144; transverse study). Maximal oxygen consumption (VO_2max, direct method), mechanical power at (VO_2max ( ), maximal anaerobic power (P_max; force-velocity test), mean power in 30-s sprint (P _30s; Wingate test) were evaluated and the ratios between P_max,P _30s and were calculated. Sexual maturation was determined using salivary testosterone as an objective indicator. Normalized for body massVO_2max remained constant from 6 to 15 years (49 ml· min^–1 · kg^–1, SD 6), whilst P_max andP _30s increased from 6–8 to 14–15 years, from 6.2 W · kg^–1, SD 1.1 to 10.8 W · kg^–1, SD 1.4 and from 4.7 W · kg^–1, SD 1.0 to 7.6 W · kg^–1, SD 1.0, respectively, (P < 0.001). The ratio P_max: was 1.7 SD 3.0 at 6–8 years and reached 2.8 SD 0.5 at 14–15 years and the ratioP _30s: changed similarly from 1.3 SD 0.3 to 1.9 SD 0.3. In contrast, the ratio P_max:P _30s remained unchanged (1.4 SD 0.2). Significant relationships (P < 0.001) were observed between P_max (W · kg^–1),P _30s (W · kg^–1), blood lactate concentrations after the Wingate test, and age, height, mass and salivary testosterone concentration. This indicates that growth and maturation have together an important role in the development of anaerobic metabolism.     

Energetics of locomotion in African pygmies

Summary The energy cost of walking (C _w). and running (C _r), and the maximal O₂ consumption (VO_2max) were determined in a field study on 17 Pygmies (age 24 years, SD 6; height 160 cm, SD 5; body mass 57.2 kg, SD 4.8) living in the region of Bipindi, Cameroon. TheC _w varied from 112 ml·kg^–1·km^–1, SD 25 [velocity (), 4 km·h^–1] to 143 ml·kg^–1·km^–1, SD 16 (, 7 km·h^–1). Optimal walking was 5 km·h^–1. TheC _r was 156 ml·kg^–1·km^–1, SD 14 (, 10 km·h^–1) and was constant in the 8–11 km·h^–1 speed range. TheVO_2max was 33.7 ml·kg^–1· min^–1, i.e. lower than in other African populations of the same age. TheC _r andC _w were lower than in taller Caucasian endurance runners. These findings, which challenge the theory of physical similarity as applied to animal locomotion, may depend either on the mechanics of locomotion which in Pygmies may be different from that observed in Caucasians, or on a greater mechanical efficiency in Pygmies than in Caucasians. The lowC _r values observed enable Pygmies to reach higher running speeds than would be expected on the basis of theirVO_2max.     

The relative influence of body characteristics on humid heat stress response

The present study was designed to determine the relative importance of individual characteristics such as maximal oxygen uptake ( O_2max), adiposity, DuBois body surface area (A _D), surface to mass ratio (A _D: mass) and body mass, for the individual's reaction to humid heat stress. For this purpose 27 subjects (19 men, 8 women), with heterogeneous characteristics ( O_2max 1.86–5.28 1 · min^–1; fat% 8.0%–31.9%; mass 49.8–102.1 kg; A _D 1.52–2.33 m²) first rested (30 min) and then exercised (60 W for 1 h) on a cycle ergometer in a warm humid climate (35°C, 80% relative humidity). Their physiological responses at the end of exercise were analysed to assess their relationship with individual characteristics using a stepwise multiple regression technique. Dependent variables (with ranges) included final values of rectal temperature (T _re 37.5–39.0°C), mean skin temperature (T _sk 35.7–37.5°C), body heat storage (S 3.2–8.1 J · g^–1), heart rate (HR 100–172 beat · min^–1), sweat loss (397–1403g), mean arterial blood pressure (BP_a, 68–96 mmHg), forearm blood flow (FBF, 10.1–33.9 ml · 100ml^–1 · min^–1) and forearm vascular conductance (FVC = FBF/BP_a, 0.11–0.49 ml · 100 ml^–1 · min^–1 · mmHg^–1). The T _re, T _sk and S were (34%–65%) determined in the: main by ( O_2max), or by exercise intensity expressed as a percent age of O_2max (% O_2max). For T _re, A _D: mass ratio also contributed to the variance explained, with about half the effect of ( O_2max), For T _sk, fat% contributed to the variance explained with about two-third the effect of O_2max. Total body sweat loss was highly dependent (50%) on body size (A _D or mass) with regular activity level having a quarter of the effect of body size on sweat loss. The HR, similar to T _re, was determined by O_2max (48%–51%), with less than half the effect of A _D or A _D :mass (20%). Other circulatory parameters (FBF, BP_a, FVC) showed little relationship with individual characteristics ( < 36% of variance explained). In general, the higher the ( O_2max), and/or the bigger the subject, the lower the heat strain observed. The widely accepted concept, that body core temperature is determined by exercise intensity expressed as % O_2max and sweat loss by absolute heat load, was only partially supported by the results. For both variables, other individual characteristics were also shown to contribute.     

Occurrence of electromyographic and ventilatory thresholds in professional road cyclists

The temporal relationship between the electromyographic (EMG) and ventilatory thresholds was investigated during incremental exercise performed by eight professional road cyclists. The exercise, performed on a cycloergometer, started at 100 W with successive increments of 26 W·min^–1 until exhaustion. Gas exchange and the root mean square value of EMG (RMS) from eight lower limb muscles were examined throughout the exercise period. Professional cyclists achieved a maximal oxygen consumption, i.e. O_2max, of 5.4 (0.5) l·min^–1 [74.6 (2.5) ml·min^–1·kg^–1, range: 67.8–82.4 ml·min^–1·kg^–1] and a maximum power (W_max) of 475 (30) W (range: 438–516 W). Our results showed at least the occurrence of a first EMG threshold (EMG_Th1) in 50% (gastrocnemius lateralis) of the subjects and a second EMG threshold (EMG_Th2) in 63% (gastrocnemius medialis). EMG_Th1 occurred significantly before the first ventilatory threshold (VT₁), i.e. at 52 (2)% and 62 (9)% of W_max, respectively. Inversely, no significant difference was observed between the occurrence of EMG_Th2 and the second ventilatory threshold (VT₂), i.e. at 86 (1)% and 89 (7)% of W_max, respectively. These results suggest that the use of EMG may be a useful non-invasive method for detecting the second ventilatory threshold in most of the muscles involved in cycling exercise.     

Finger and forearm vasodilatatory changes after local cold acclimation

Summary To determine the vascular changes induced by local cold acclimation, post-ischaemia and exercise vasodilatation were studied in the finger and the forearm of five subjects cold-acclimated locally and five non-acclimated subjects. Peak blood flow was measured by venous occlusion plethysmography after 5 min of arterial occlusion (PBF_isc), after 5 min of sustained handgrip at 10% maximal voluntary contraction (PBF_exe), and after 5 min of both treatments simultaneously (PBF_isc+exe). Each test was performed at room temperature (25° C, SE 1 C) (non-cooled condition) and after 5 min of 5'C cold water immersion (cooled condition). After the cold acclimation period, the decrease in skin temperature was more limited in the cold-acclimated compared to the non-acclimated (P<0.01). The PBF_isc was significantly reduced in the cooled condition only in the cold-acclimated subjects (finger: 8.4 ml · 100 ml^–1 · min^–1, SE 1.1,P<0.01; forearm: 5.8 ml · 100 ml^–1 · min^–1, SE 1.5,P<0.01) compared to the non-cooled condition. Forearm PBF_exe was significantly decreased in the cooled condition only in the cold-acclimated subjects (non-cooled: 7.4 ml · 100 ml^–1 · min^–1, SE 1.2; cooled: 3.9 ml · 100 ml^–1 ·min^–1, SE 2.6,P<0.05) indicating that muscle blood flow was also reduced. The application of PBF_isc+exe elicited an increase in peak blood flow only in the forearm of the non-acclimated subjects (non-cooled: 10.4 ml· 100 ml^–1 · min^–1, SE 2.0; cooled: 14.3 ml · 100 ml^–1 · min^–1, SE 2.6,P<0.05) and conversely only in the finger of the cold-acclimated (non-cooled finger: 25.7 ml · 100 ml^–1 · min^–1, SE 4.4; cooled finger: 19.2 ml · 100 ml^–1 · min^–1, SE 3.3,P<0.01). Therefore, subjects cold-acclimated locally showed decreased vasodilatatory responses only when exposed to cold.     

Treadmill validation of an over-ground walking test to predict peak oxygen consumption

Summary The purpose of this study was to determine whether a test developed to predict maximal oxygen consumption (VO_2max) during over-ground walking, was similarly valid as a predictor of peak oxygen consumption (VO₂) when administered during a 1-mile (1.61 km) treadmill walk. Treadmill walk time, mean heart rate over the last 2 full min of the walk test, age, and body mass were entered into both generalized (GEN Eq.) and gender-specific (GSP Eq.) prediction equations. Overall results indicated a highly significant linear relationship between observed peakVO₂ and GEN Eq. predicted values (r=0.91), a total error (TE) of 5.26 ml · kg^–1 · min^–1 and no significant difference between observed and predicted peakVO₂ mean values. The peakVO₂ for women (n = 75) was predicted accurately by GSP Eq. (r = 0.85; TE = 4.5 ml · kg^–1 · min^–1), but was slightly overpredicted by GEN Eq. (overall mean difference = 1.4 ml · kg^–1 · min^–1;r=0.86; TE = 4.56 ml · kg^–1 · min^–1). No significant differences between observed peakVO₂ and either GEN Eq. (r=0.85; TE=4.3 ml · kg^–1 · min^–1) or GSP Eq. (r=0.85; TE = 4.8 ml · kg^–1 · min^–1)predicted values were noted for men (n=48) with peakVO₂ values less than or equal to 55 ml · kg^–1 · min^–1. However, both equations significantly underpredicted peakVO₂ for the remaining high peakVO₂ men (n = 22). In conclusion, the over-ground walking test, when administered on a treadmill, is a valid method of predicting peakVO₂ but underpredicts peakVO₂ of subjects with observed high peakVO₂ values. Present address: Human Performance Laboratory State University, Muncie, IN 47306, USA