Exercise-induced changes in blood levels of alpha-tocopherol

Levels of α-tocopherol (αT) in plasma and red blood cells (RBC) are assumed to be modulated by exercise. The mechanisms involved remain to be established. We examined the influence of different running bouts on the content of αT in RBC (αT_RBC), the concentration in plasma (αT_plasma), and their relationship with lipolysis, as indicated by changes (Δ) in plasma glycerol concentration ([glycerol]). Eleven healthy runners [mean (SD) age 35 (9) years, height 177.3 (7.6) cm, body mass 69.6 (9.4) kg, and peak oxygen consumption, , 57.8 (4.8) ml^.kg^–1.min^–1] performed an incremental treadmill test [duration 17 (2) min, peak velocity, v _peak 4.8 (0.4) m^.s^–1], a training run [173 (12) min, 57 (4)% v _peak] and a marathon [197 (24) min, 75 (5)% v _peak]. Before (pre) and after (post) each run, haematological and lipid parameters, αT_RBC and αT_Plasma were determined. Haemoconcentration was observed after each run. Δ[glycerol] was +0.10 (0.10) mmol^.l^–1, +0.40 (0.14) mmol^.l^–1 and +0.51 (0.15) mmol^.l^–1 in the treadmill test, training run and marathon, respectively. When corrected for haemoconcentration, values of αT_plasma decreased [–5.4 (7.5)%, P<0.05] in the treadmill test, were unchanged [+0.7 (8.7)%] in the training run and increased [+7.8 (8.3)%, P<0.05] in the marathon. αT_RBC decreased [pre vs post: 22.7 (3.2) nmol^.g haemoglobin^–1 (nmol^.g Hb^–1) vs 18.9 (3.8) nmol^.g Hb^–1, P<0.05] in the treadmill test and was not significantly changed in either the training run [20.8 (1.9) nmol^.g Hb^–1 vs 19.1 (3.0) nmol^.g Hb^–1] or the marathon [21.6 (2.9) nmol^.g Hb^–1 vs 23.4 (2.7) nmol^.g Hb^–1]. ΔαT_RBC and ΔαT_plasma were positively related to Δ[glycerol]. The reduction in αT_RBC and αT_plasma after short-lasting heavy exercise indicates the consumption of αT, whereas the association between ΔαT and Δ[glycerol] suggests mobilisation of αT, especially in long-lasting exercises. However, although αT appears to be influenced by exercise, the results suggest a well-balanced regulation of αT during exercise resulting in small, and only in part, significant ΔαT in blood. Electronic Publication     

Cardiorespiratory responses to exercise in acute hypoxia, hyperoxia and normoxia

There is a prevailing hypothesis that an acute change in the fraction of oxygen in inspired air (F _IO₂) has no effect on maximal cardiac output ( ), although maximal oxygen uptake ( ) and exercise performance do vary along with F _IO₂. We tested this hypothesis in six endurance athletes during progressive cycle ergometer exercise in conditions of hypoxia (F _IO₂=0.150), normoxia (F _IO₂=0.209) and hyperoxia (F _IO₂=0.320). As expected, decreased in hypoxia [mean (SD) 3.58 (0.45) l·min^–1, P<0.05] and increased in hyperoxia [5.17 (0.34) l·min^–1, P<0.05] in comparison with normoxia [4.55 (0.32) l·min^–1]. Similarly, maximal power ( ) decreased in hypoxia [334 (41) W, P<0.05] and tended to increase in hyperoxia [404 (58) W] in comparison with normoxia [383 (46) W]. Contrary to the hypothesis, was 25.99 (3.37) l·min^–1 in hypoxia (P<0.05 compared to normoxia and hyperoxia), 28.51 (2.36) l·min^–1 in normoxia and 30.13 (2.06) l·min^–1 in hyperoxia. Our results can be interpreted to indicate that (1) the reduction in in acute hypoxia is explained both by the narrowing of the arterio-venous oxygen difference and reduced , (2) reduced in acute hypoxia may be beneficial by preventing a further decrease in pulmonary and peripheral oxygen diffusion, and (3) reduced and in acute hypoxia may be the result rather than the cause of the reduced and skeletal muscle recruitment, thus supporting the existence of a central governor. Electronic Publication     

Hyperpnoea and CO2 sensitivity of the respiratory centres during exercise

Summary The aim of this study was to specify whether exercise hyperpnoea was related to the CO₂ sensitivity of the respiratory centres measured during steady-state exercise of mild intensity. Thus, ventilation , breathing pattern [tidal volume (V _T), respiratory frequency (f), inspiratory time (T _I), total time of the respiratory cycle (T _TOT),V _T/T _I,T _I/T _TOT] and CO₂ sensitivity of the respiratory centres determined by the rebreathing method were measured at rest (SCO_{2 re}) and during steady-state exercise (SCO_{2 ex}) of mild intensity [CO₂ output =20 ml·kg⁻¹·min⁻¹] in 11 sedentary male subjects (aged 20–34 years). The results showed that SCO_{2 re} and SCO_{2 ex} were not significantly different. During exercise, there was no correlation between and SCO_{2 ex} and, for the same , all subjects had very close values normalized for body mass (bm), regardless of their SCO_{2 ex} ( =1.44 l·min⁻¹·kg⁻¹ SD 0.10). A highly significant positive correlation between SCO_{2 ex} andV _T (normalised for bm) (r=0.80,P<0.01),T _I (r=0.77,P<0.01) andT _TOT (r=0.77,P<0.01) existed, as well as a highly significant negative correlation between SCO_{2 ex} and (normalised for bm^−0.25) (r=−0.73,P<0.01). We conclude that the hyperpnoea during steady-state exercise of mild intensity is not related to the SCO_{2 ex}. The relationship between breathing pattern and SCO_{2 ex} suggests that the breathing pattern could influence the determination of the SCO_{2 ex}. This finding needs further investigation.     

Modulation of the transient outward K+ current by inhibition of endothelin-A receptors in normal and hypertrophied rat hearts

Inhibition of endothelin-A (ET_A) receptors has been shown to reduce ventricular electrical abnormalities associated with cardiac failure. In this study, we investigate the effect of ET_A-receptor inhibition on the development of regional alterations of the transient outward K⁺ current (I _to) in the setting of pressure-induced left ventricular (LV) hypertrophy. Cardiac hypertrophy was induced in female Sprague–Dawley rats by stenosis of the ascending aorta (AS) for 7 days. Treatment with the selective ET_A-receptor antagonist darusentan (LU135252, 35 mg [kg body weight]⁻¹ day⁻¹) was started 1 day before the surgery. AS induced a 46% increase in the relative LV weight (p < 0.001) and caused a significant reduction in I _to (at +40 mV) in epicardial myocytes (19.5 ± 1.2 pA pF⁻¹, n = 32 vs 23.2 ± 1.2 pA pF⁻¹, n = 35, p < 0.05). Darusentan further reduced I _to in AS (15.4 ± 1.3 pA pF⁻¹, n = 37, p < 0.05) and sham-operated animals (19.8 ± 1.6 pA pF⁻¹, n = 48, ns.). The effects of AS and darusentan on I _to were significant and independent as tested by two-way analysis of variance. I _to was not affected in endocardial myocytes. These results indicate that endothelin-1 may exert a tonic effect on the magnitude of I _to in the epicardial region of the left ventricle but that ET_A-receptor activation is not necessary for the development of electrical alterations associated with pressure-induced hypertrophy.     

Effect of water ingestion on cardiovascular and thermal responses to prolonged cycling and running in humans: a comparison

The aim of this investigation was to examine the effect of water ingestion on physiological responses to prolonged cycling (CYC) and running (RUN). A group of 11 men with mean (SEM) maximal oxygen uptake (V˙O_2max) 48.5 (1.8) ml·kg^–1·min^–1 on a cycle-ergometer and 52.1 (2.2) ml·kg^–1·min^–1 on a treadmill (P<0.01) exercised for 90 min on four occasions, twice on each ergometer, at 60% of mode specific V˙O_2max. No fluid was taken (D) in one trial on each ergometer, whereas 60% of fluid losses were replaced by drinking water in the other trial (W). In CYC, water ingestion attenuated the change in cardiac output ( ) and the reduction in stroke volume (ΔSV) [ΔSV: –22.7 (3.8) in D, –10.7 (2.9) ml·beat^–1 in W, P<0.01; : –1.9 (0.5) in D, –0.2 (0.4) l·min^–1 in W at 85 min, P<0.01], but did not affect rectal temperature [T _re at 90 min: 38.8 (0.1)°C in D, 38.7 (0.1)°C in W]. In contrast, fluid replacement reduced hyperthermia in RUN [T _re at 90 min: 39.6 (0.2) in D, 39.1 (0.2)°C in W, P<0.01], and this was linked with a higher skin blood flow [RUN-W 88.9 (8.5), RUN-D 70.7 (8.4)%, P<0.05]. The and ΔSV were also attenuated with water ingestion in this mode of exercise (P<0.05). It is concluded that water ingestion improves physiological function in both cycling and running, but that the underlying mechanism is different in the two modes of exercise. Electronic Publication     

A calcium-dependent chloride current in insulin-secreting βTC-3 cells

 Ca²⁺-dependent conductances have been hypothesized to play a role in the bursting pattern of electrical activity of insulin-secreting β cells in response to high plasma glucose. A Maxi K⁺ channel has received the most attention, while a low-conductance Ca²⁺-activated K⁺ current has also been identified. We used an increasingly popular β cell model system, the βTC-3 cell line, and the perforated-patch technique to describe the properties of a novel Ca²⁺-dependent Cl^–current [I _Cl(Ca)] in insulin-secreting pancreatic β cells. The reported I_Cl(Ca) could be activated under physiological Ca²⁺ concentrations and is the first of its kind to be described in pancreatic insulin-secreting cells. We found that long depolarizing steps above –20 mV elicited an outward current which showed slow inward relaxation upon repolarization to negative membrane potentials. Both the outward currents and the inward tails showed dependence on Ca²⁺ influx: their current/voltage (I/V) relations followed that of the ”L-like” Ca²⁺ current (I _Ca) present in these cells; they were blocked completely by the removal of external Ca²⁺ or application of Cd²⁺ at concentrations sufficient for complete block of I _Ca; and their magnitude increased with the depolarizing step duration. Moreover, the inward tail decayed monoexponentially with a time constant which at voltages negative to activation of I _Ca showed a weak linear voltage dependence, while at voltages positive to activation of I _Ca it followed the voltage dependence of I _Ca. This Ca²⁺-dependent current reversed at –21.5 mV and when the external Cl^–concentration was reduced from 159 mM to 62 mM the reversal potential shifted by ≈+20 mV as predicted by the Nernst relation for a Cl^–-selective current. Cl^–channel blockers such as DIDS (100 μM) and niflumic acid (100 μM) blocked this current. We concluded that this current was a Ca²⁺-dependent Cl^–current [I _Cl(Ca)]. From substitution of the external Cl^–with various monovalent anions and from the reversal potentials we obtained the following permeability sequence for I _Cl(Ca): I ^–>NO₃ ^–>Br^–>Cl^–>Acetate^–. Received: 10 October 1996 / Received after revision and accepted: 19 December 1996     

Prediction of sprint triathlon performance from laboratory tests

This study investigated whether sprint triathlon performance can be adequately predicted from laboratory tests. Ten triathletes [mean (SEM), age 21.8 (0.3) years, height 179 (2) cm, body mass 67.5 (2.5) kg] performed two graded maximal exercise test in random order, either on their own bicycle which was mounted on an ergometer or on a treadmill, to determine their peak oxygen consumption (O₂peak). Furthermore, they participated in two to three 30-min constant-load tests in both swimming, cycling and running to establish their maximal lactate steady state (MLSS) in each exercise mode. Swim tests were performed in a 25-m swimming pool (water temperature 27°C). During each test heart rate (HR), power output (PO) or running/swimming speed and blood lactate concentration (BLC) were recorded at regular intervals. Oxygen uptake (O₂) was continuously measured during the graded tests. Two weeks after the laboratory tests all subjects competed in a triathlon race (500 m swim, 20-km bike, 5-km run) [1 h 4 min 45 s (1 min 38 s)]. Peak HR was 7 beats·min^–1 lower in the graded cycle test than in the treadmill test (p<0.05) at similar peak BLC (~10 mmol·l^–1) and O₂peak (~5 L·min^–1). High correlations were found between O₂peak during cycling (r=–0.71, p<0.05) or running (r=–0.69, p<0.05) and triathlon performance. Stepwise multiple regression analysis showed that running speed and swimming speed at MLSS, together with BLC in running at MLSS, yielded the best prediction of performance [1 h 5 min 18 s (1 min 49 s)]. Thus, our data indicate that exercise tests aimed to determine MLSS in running and swimming allow for a precise estimation of sprint triathlon performance.     

Core temperature thresholds for hyperpnea during passive hyperthermia in humans

Humans have higher ventilation when they are hyperthermic but it is not known whether core temperature thresholds for ventilation exist, nor has a physiological rationale been presented for this response. To examine this question, ventilation was studied in relation to core temperatures in humans rendered hyperthermic in a warm bath. Seven subjects [mean (SE), 23.3 (1.4) years] wearing only shorts and a thick felt hat with ear flaps were immersed to the neck in a bath at 41 (0.5)°C for 25 min. Tympanic (T _ty), esophageal (T _es), thigh skin and forehead skin temperatures, heart rate, inspired minute ventilation (V _I at body temperature and pressure, saturated), ventilation frequency and oxygen consumption (VO₂ at standard temperature and pressure, dry) were recorded at 30-s intervals. At immersion V _I briefly increased to 18.6 (3.0)l·min^–1 returned to about the pre-immersion value,, and significantly increased to 19.3 (3.0) l·min^–1 by the end of immersion. VO₂ increased significantly from the pre-immersion value of 0.27 l·min^–1 to 0.67 l·min^–1 by the first 0.5 min of immersion, but then returned to its pre-immersion value. T _ty increased to 38.7 (0.2)°C and T _es increased to 39.0 (0.2)°C by the end of immersion. Core temperature thresholds for increases in V _I were evident at 38.1°C when expressed against T _ty and at 38.5°C when expressed against T _es. The results indicated that during body warming core temperature thresholds for V _I are reached and subsequently a hyperpnea was evident, despite VO₂ remaining at a resting value. This hyperpnea is seen as a thermoregulatory response likely to participate in selective brain cooling.     

A hyperpolarization-activated cation current (I h) contributes to resting membrane potential in rat superior cervical sympathetic neurones

 Using perforated-patch voltage-clamp recording, a prominent hyperpolarization-activated inward cation current (I _h) has been identified in dissociated, cultured and replated, superior cervical sympathetic (SCG) neurones from 17-day-old rats. I _h was identified as a slowly activated inward current on hyperpolarizing from –60 mV, with an extrapolated null potential (in 3 mM [K⁺]_out) of –42 mV. The activation range for I _h was –40 to –100 mV, with a half-activation voltage (V _0.5) of –63 mV. The current was suppressed by 1 mM Cs⁺ but not by 1 mM Ba²⁺. The reversal potential for the current change induced by Cs⁺ agreed with the null potential for I _h. I _h conferred strong inward rectification to the current-voltage curve negative to –55 mV in both voltage-clamp and current-clamp recording. This inward rectification was reduced by 1 mM Cs⁺. In a sample of eight cells with initial resting membrane potentials between –51 and –64 mV, Cs⁺ increased the resting potential of all cells by between 2.5 and 21 mV. These results indicate that I _h contributes a tonic inward (depolarizing) component to the maintenance of the resting membrane potential in SCG neurones. Received: 16 January 1998 / Received after revision and accepted: 1 April 1998     

An increase in [Ca2+]i activates basolateral chloride channels and inhibits apical sodium channels in frog skin epithelium

 The aim of this study was to investigate the mechanisms by which increases in free cytosolic calcium ([Ca²⁺]_i) cause a decrease in macroscopic sodium absorption across principal cells of the frog skin epithelium. [Ca²⁺]_i was measured with fura-2 in an epifluorescence microscope set-up, sodium absorption was measured by the voltage-clamp technique and cellular potential was measured using microelectrodes. The endoplasmic reticulum calcium-ATPase inhibitor thapsigargin (0.4 μM) increased [Ca²⁺]_i from 66 ± 9 to 137 ± 19 nM (n = 13, P = 0.002). Thapsigargin caused the amiloride-sensitive short circuit current (I _sc) to drop from 26.4 to 10.6 μA cm^–2 (n = 19, P<0.001) concomitant with a depolarization of the cells from –79 ± 1 to –31 ± 2 mV (n = 18, P<0.001). Apical sodium permeability (P ^a _Na) was estimated from the current/voltage (I/V) relationship between amiloride-sensitive current and the potential across the apical membrane. P ^a _Na decreased from 8.01·10^–7 to 3.74·10^–7 cm s^–1 (n = 7, P = 0.04) following an increase in [Ca²⁺]_i. A decrease in apical sodium permeability per se would tend to decrease I _sc and result in a hyperpolarization of the cell potential and not, as observed, a depolarization. Serosal addition of the chloride channel inhibitors 4,4′-diisothiocyanatostilbene-2,2′-disulphonic acid (DIDS), diphenylamine-2-carboxylate (DPC), indanyloxyacetic acid 94 (IAA-94) and furosemide reversed the depolarization induced by thapsigargin, indicating that chloride channels were activated by the increase in [Ca²⁺]_i. This was confirmed in wash-out experiments with ³⁶Cl where it was shown that thapsigargin increased the efflux of chloride from 32.49 ± 5.01 to 62.63 ± 13.3 nmol·min^–1 cm^–2 (n = 5, P = 0.04). We conclude that a small increase in [Ca²⁺]_i activates a chloride permeability and inhibits the apical sodium permeability. The activation of chloride channels and the closure of apical sodium channels will tend to lower the macroscopic sodium absorption. Received: 25 June 1996 / Received after revision: 28 August 1996 / Accepted: 2 September 1996     

Actions of myristyl-FRCRCFa, a cell-permeant blocker of the cardiac sarcolemmal Na-Ca exchanger, tested in rabbit ventricular myocytes

 In cardiac muscle, the electrogenic Na-Ca exchanger plays important roles in determining action potential shape and in the beat-to-beat homeostasis of intracellular calcium. In this study we tested the actions of a putative cell-permeant blocker of the cardiac sarcolemmal Na-Ca exchange, ”Myristyl- (Myr-) FRCRCFa”. Experiments were performed using isolated rabbit right ventricular myocytes and whole-cell patch-clamp at 35–37°C. The Na-Ca exchange current (I _Na-Ca), L-type calcium current (I _Ca,L), inward rectifier potassium current (I _K1) and delayed rectifier potassium current (I _K) were compared in untreated cells and cells incubated in a solution containing N-myristylated FRCRCFa. With other major currents blocked, I _Na-Ca was measured as the Ni-sensitive component of current during a voltage ramp applied from the holding potential of –40 mV, between +80 and –120 mV (ramp velocity 0.1 V s^–1). In untreated cells, I _Na-Ca at +60 mV was 7.1±0.6 pA/pF and at –100 mV was –2.7±0.3 pA/pF (n=9). After a 15-min pre-incubation with 20 μM Myr-FRCRCFa, I _Na-Ca was reduced to 4.2±0.3 pA/pF at +60 mV and –1.5±0.2 pA/pF at –100 mV (P<0.02; n=7). After incubation with 20 μM Myr-FRCRCFa for 1 h, I _Na-Ca at both potentials was further reduced (2.3±0.8 pA/pF at +60 mV; –0.9±0.3 pA/pF at –100 mV; P<0.008 compared with control; n=4). Under selective recording conditions for I _Ca,L, there was little difference in I _Ca,L density between untreated and cells incubated with Myr-FRCRCFa. A Boltzmann fit to the I _Ca,L/V relation showed no significant alteration of half-maximal activation potential or slope factor of activation. I _K1 was also largely unaffected by pre-incubation of cells with Myr-FRCRCFa. I _K, measured as deactivating tail current following 1-s test depolarisations to a range of test potentials, was also not significantly altered by Myr-FRCRCFa. The suppression of I _Na-Ca in cells incubated in Myr-FRCRCFa suggests that addition of the myristyl group to FRCRCFa peptide conveys cell permeancy to the peptide and that Myr-FRCRCFa applied externally to rabbit ventricular myocytes is moderately effective as an I _Na-Ca blocker. I _Ca,L, I _K1 and I _K were largely unaffected by Myr-FRCRCFa. N-Myristylation of such conformationally constrained hexapeptides may, therefore, provide a means of producing cell-permeant inhibitors of the cardiac Na-Ca exchanger. Received: 6 February 1997 / Received after revision: 8 April 1998 / Accepted: 9 April 1998     

Ventilatory response of prepubertal boys and adults to carbon dioxide at rest and during exercise

Summary The aim of this study was to determine whether the greater ventilation in children at rest and during exercise is related to a greater CO₂ ventilatory response. The CO₂ ventilatory response was measured in nine prepubertal boys [10.3 years (SD 0.1)] and in 10 adults [24.9 years (SD 0.8)] at rest and during moderate exercise ( CO₂ = 20 ml·kg^–1·min^–1) using the CO₂-rebreathing method. Three criteria were measured in all subjects to assess the ventilatory response to CO₂: the CO₂ sensitivity threshold (Th), which was defined as the value of end titalPCO₂ (P _ETCO₂) where the ventilation increased above its steady-state level; the reactivity slope expressed per unit of body mass (SBM), which was the slope of the linear relation between minute ventilation ( _E) andP _ETCO₂ above Th; and the slope of the relationship between the quotient of tidal volume (V _T) and inspiration time (t _I) andP _ETCO₂ (V _T ·t _I ^–1 ·P _ETCO₂ ^–1) values above Th. The _E,V _T, breathing frequency (f _R), oxygen uptake ( O₂), and CO₂ production ( CO₂) were also measured before the CO₂-rebreathing test. The following results were obtained. First, children had greater ventilation per unit body weight than adults at rest (P<0.001) and during exercise (P<0.01). Second, at rest, onlyV _T ·t _I ^–1 ·P _ETCO₂ ^–1 was greater in children than in adults (P<0.001). Third, during exercise, children had a higher S_BM (P < 0.02) andV _T ·t _I ^–1 ·P _ETCO₂ ^–1 (P<0.001) while Th was lower (P<0.02). Finally, no correlation was found between _E/ CO₂ and Th while a significant correlation existed between _E/ CO₂ and S_BM (adults,r=0.79,P<0.01; children,r=0.73,P<0.05). We conclude that children have, mainly during exercise, a greater sensitivity of the respiratory centres than adult. This greater CO₂ sensitivity could partly explain their higher ventilation during exercise, though greater CO₂ production probably plays a role at rest.     

Is exhaustive training adequate preparation for endurance performance?

Summary Our purpose was to test the significance of exhaustive training in aerobic or endurance capacity. The extent of adaptations to endurance training was evaluated by assessing the increase in physical performance capability and oxidative markers in the organs of rats trained by various exercise programs. Rats were trained by treadmill running 5 days · week^–1 at 30 m · min^–1 for 8 weeks by one of three protocols:T ₁ — 60 min · day^–1;T ₂ — 120 min · day^–1; andT ₃ — 120 min · day^–1 (3 days · week^–1) and to exhaustion (2 days · week^–1). GroupsT ₂ andT ₃ ran for longer thanT ₁ in an endurance exercise test (P<0.05), in which the animals ran at 30 m · min^–1 to exhaustion; no difference was observed between groupsT ₂ andT ₃. All 3 trained groups showed a similar increase (20–27%) in the fast-twitch oxidative-glycolytic (FOG) fibers with a concomitant decrease in the fast-twitch glycolytic (FG) fiber population in gastrocnemius (p<0.05). The capillary supply in gastrocnemius increased with the duration of exercise (p<0.05): no difference was found between groupsT ₂ andT ₃. Likewise, no distinction was seen between groupsT ₂ andT ₃ in the increase in succinate dehydrogenase activity in gastrocnemius and the heart. These results suggest that the maximal adaptive response to endurance training does not require daily exhaustive exercise.     

Maintenance of testosterone status in fitness joggers after increased training mileage

The primary objective was to evaluate the early effect of increased training mileage on testosterone (T) status in recreational joggers. Serum total (T_tot) and free (T_free) concentrations at rest, overnight urinary T_tot excretion, and the T_tot and T_free responses to maximal exercise were used as indicators of T status. A group of 13 male [mean (SD) age 24.5 (2.5) years] fitness joggers [maximal oxygen consumption, , 52.9 (4.9) ml·kg^–1·min^–1] qualified as subjects. The training intervention consisted of a 100% increase in the habitual distance run [12 (3) miles·week^–1] for 2 consecutive weeks, while maintaining the customary training intensity. Blood samples were obtained at rest and after maximal exercise tests, at the beginning and end of a control week of habitual jogging (baseline) and also following the 1st and 2nd weeks of the intervention. The and treadmill exercise endurance time were unchanged across sampling times. Serum T_tot and T_free concentrations averaged 565 (62) and 24 (2.6) ng·dl^–1, respectively, at baseline and did not change significantly. Urinary T_tot excretion averaged 1.5 (0.21) ng·min^–1 at baseline, and also remained unchanged during the intervention. Relative increases in T_tot (23%) and T_free (22%) were observed following maximal exercise compared to rest (P<0.05). However, the exercise-related increases in serum T_tot and T_free were not evident after adjustment for the change in plasma volume. It was concluded, that the training intervention did not alter T status in these fitness joggers. Electronic Publication     

Pressure and coverage effects of sporting compression garments on cardiovascular function,thermoregulatory function,and exercise performance

Sporting compression garments (CG) are used widely during exercise despite little evidence of benefits. The purpose of this study was to investigate coverage and pressure effects of full-body CG on cardiovascular and thermoregulatory function at rest and during prolonged exercise, and on exercise performance. Twelve recreationally trained male cyclists [mean (SD) age, 26 (7) years; [(V)\dot]\textO_2max \dot{V}{\text{O}}_{2\max } , 53 (8) mL kg⁻¹ min⁻¹] completed three sessions (counterbalanced order), wearing either correctly-sized CG (CSG; 11–15 mmHg), over-sized CG (OSG; 8–13 mmHg), or gym shorts (CONT). Test sessions were conducted in temperate conditions [24 (1)°C, 60 (4)% relative humidity; ~2 m s⁻¹ air velocity during exercise], consisting of resting on a chair then on a cycle ergometer, before 60-min fixed-load cycling at ~65% [(V)\dot]\textO_2max \dot{V}{\text{O}}_{2\max } and a 6-km time trial. Wearing CG (CSG or OSG) did not mitigate cardiovascular strain during mild orthostatic stress at rest (p = 0.20–0.93 for garment effects). During exercise, cardiac output was ~5% higher in the CG conditions (p < 0.05), which appears to be accounted for via non-significant higher end-exercise heart rate (~4–7%, p = 0.30; p = 0.06 for greater heart rate drift in CSG); other cardiovascular variables, including stroke volume, were similar among conditions (p = 0.23–0.91). Covered-skin temperature was higher in CG conditions (p < 0.001) but core (oesophageal) temperature was not (p = 0.79). Time-trial performance (mean power, time taken) was similar with or without CG (p = 0.24–0.44). In conclusion, any demonstrable physiological or psychophysical effects of full-body CG were mild and seemingly reflective more of surface coverage than pressure. No benefit was evident for exercise performance.     

Relationship between muscle T2 * relaxation properties and metabolic state: a combined localized 31P-spectroscopy and 1H-imaging study

A multi-volume ³¹P-magnetic resonance spectroscopy localization procedure was implemented to compare directly muscle metabolism and proton T₂ ^* relaxation properties in the human plantar flexor muscles during exercise. Localized ³¹P-spectra were collected simultaneously from the medial gastrocnemius, lateral gastrocnemius and soleus muscles during exercise using β ₁-insensitive Hadamard Spectroscopic Imaging (HSI). ¹H T₂ ^*-weighted gradient-echo images were acquired at rest and immediately following high-intensity plantar flexion exercise. T₂ ^* mapping of the individual calf muscles showed that plantar flexion with the knee extended produces significant increases (P < 0.0001) in the mean (SEM) T₂ ^* of the medial [35.6 (1.2) ms vs 28.5 (0.5) ms at rest] and lateral gastrocnemius [35.6 (0.9) ms vs 26.2 (0.9) ms at rest], but not in the soleus [26.7 (0.6) ms vs 27.3 (0.8) ms at rest]. In accordance with the changes in T₂ ^*, the ratio of inorganic phosphate to phosphocreatine (P_i:PCr) and the intracellular muscle pH shifted significantly in the gastrocnemii, while the soleus showed no change in muscle pH and only a moderate increase in P_i-to-Ph. Comparison of spectroscopic and relaxation parameters in both gastrocnemius muscles revealed a significant relationship between post-exercise T₂ ^* and intracellular pH (r=0.72–0.76) and P_i-to-Ph ratios (r=0.81–0.88) during exercise. Using an improved method of localization, this study confirms the existence of a strong relationship between transverse relaxation properties and the metabolic state in skeletal muscles engaged in heavy exercise. Accepted: 28 December 1999     

Differences between swimming and running as stimuli for exercise-induced asthma

Summary Thirteen children each exercised for 6 min by running on a treadmill and by tethered swimming, breathing air at room temperature and either 8% or 99% relative humidity continuously. Ventilation, gas exchange and heart rate were closely matched in all four tests in each child, with a mean oxygen consumption of 32.3±1.7ml·min^–1·kg^–1. The post-exercise fall in FEV₁ expressed as a percentage of the baseline FEV₁ (FEV₁) was significantly greater after running compared with swimming breathing either humid or dry air. The FEV₁ was also related to respiratory heat loss (RHL) calculated from measurements of inspired and expired gas temperature and humidity. At a standardised RHL, the difference between running and swimming was highly significant [FEV₁ (%) ± SE=39±5 and 28±4 respectively, p<0.01]. These experiments suggest that the type of exercise influences the severity of exercise-induced asthma even under conditions of the same metabolic stress and respiratory heat loss.     

In a hot–dry environment racewalking increases the risk of hyperthermia in comparison to when running at a similar velocity

The purpose of this study was to determine if in a hot–dry environment, racewalking increases intestinal temperature (T_int) above the levels observed when running either at the same velocity or at a similar rate of heat production. Nine trained racewalkers exercised for 60 min in a hot–dry environment (30.0 ± 1.4°C; 33 ± 8% relative humidity; 2.4 m s⁻¹ air speed) on three separate occasions: (1) racewalking at 10.9 ± 1.0 km h⁻¹ (Walk), (2) running at the same velocity (RunVel) and (3) running at 13 ± 1.8 km h⁻¹ to obtain a similar [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} than during Walk (Run [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} ). As designed, energy expenditure rate was similar during Walk and Run [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} , but lower during RunVel (842 ± 78 and 827 ± 75 vs. 713 ± 55 W; p < 0.01). Final T_int was lower during RunVel than during both Walk and Run [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} (38.4 ± 0.3 vs. 39.2 ± 0.4 and 39.0 ± 0.4°C; p < 0.01). Heart rate and sweat rate were also lower during RunVel than during Walk and Run [(V)\dot]\textO₂ \dot{V}{\text{O}}_{2} (i.e. heart rate 159 ± 13 vs. 179 ± 11 and 181 ± 11 beats min⁻¹ and sweat rate 0.8 ± 0.3 vs. 1.1 ± 0.3 and 1.1 ± 0.3 L h⁻¹; p < 0.01). However, we could not detect differences in skin temperature among trials. In conclusion, our data indicate that in a hot–dry environment racewalking increases the risk of hyperthermia in comparison with when running at a similar velocity. However, exercise mode (walking vs. running) had no measurable impact on T_INT or heat dissipation when matched for energy expenditure.     

Prevalence and risk factors for Chlamydia trachomatis infection in adolescent females and young women in central Brazil

In order to determine the prevalence and risk factors for Chlamydia trachomatis infection in adolescent females and young women in central Brazil, 296 subjects attending two public health services were evaluated. The overall prevalence of C. trachomatis infection, as determined using polymerase chain reaction, was 19.6% (95% confidence interval [CI], 15.3–24.7). In multivariate analysis, young age (odds ratio [OR]_adjusted 2.32, 95%CI 1.1–4.8, p<0.05) and having 2–3 (OR_adjusted 3.41, 95%CI 1.6–6.3, p<0.05) or ≥4 sexual partners in life (OR_adjusted 3.10, 95%CI 1.1–6.3, p<0.05) were factors significantly associated with chlamydial infection. In conclusion, the prevalence of C. trachomatis infection was high in the studied population and risk factors were related to age and sexual behavior.     

Assessment of post-competition peak blood lactate in male and female master swimmers aged 40–79 years and its relationship with swimming performance

The main purpose of this study was to measure the post-competition blood lactate concentration ([La]_b) in master swimmers of both sexes aged between 40 and 79 years in order to relate it to age and swimming performance. One hundred and eight swimmers participating in the World Master Championships were assessed for [La]_b and the average rate of lactate accumulation (La′; mmol l⁻¹ s⁻¹) was calculated. In addition, 77 of them were also tested for anthropometric measures. When the subjects were divided into 10-year age groups, males exhibited higher [La]_b than women (factorial ANOVA, P < 0.01) and a steeper decline with ageing than female subjects. Overall, mean values (SD) of [La]_b were 10.8 (2.8), 10.3 (2.0), 10.3 (1.9), 8.9 (3.2) mmol l⁻¹ in women, and 14.2 (2.5), 12.4 (2.5), 11.0 (1.6), 8.2 (2.0) mmol l⁻¹ in men for, respectively, 40–49, 50–59, 60–69, 70–79 years’ age groups. When, however, [La]_b values were normalised for a “speed index”, which takes into account swimming speed as a percentage of world record, these sex-related differences, although still present, were considerably attenuated. Furthermore, the differences in La′ between males and females were larger in the 40–49 age group (0.34 vs 0.20 mmol l⁻¹ s⁻¹ for 50-m distance) than in the 70–79 age group (0.12 vs 0.14 mmol l⁻¹ s⁻¹ for 50-m distance). Different physiological factors, supported by the considered anthropometric measurements, are suggested to explain the results.