Exercise thermoregulation after 6 h of chair rest, 6° head-down bed-rest,and water immersion deconditioning in men

The purpose was to investigate the mechanism for the excessive exercise hyperthermia following deconditioning (reduction of physical fitness). Rectal (T _re) and mean skin ( ) temperatures and thermoregulatory responses were measured in six men [mean (SD) age, 32 (6) years; mass, 78.26 (5.80) kg; surface area, 1.95 (0.11)m²; maximum oxygen uptake ( ), 48 (6) ml·min^–1·kg^–1; whilst supine in air at dry bulb temperature 23.2 (0.6)°C, relative humidity 31.1 (11.1)% and air speed 5.6 (0.1) m·min^–1] during 70 min of leg cycle exercise [51 (4)% ] in ambulatory control (AC), or following 6 h of chair rest (CR), 6° head-down bed rest (BR), and 20° (WI20) and 80° (WI80) foot-down water immersion [water temperature, 35.0 (0.1)°C]. Compared with the AC exercise T _re [mean (SD) 0.77 (0.13)°C], T _re after CR was 0.83 (0.08)°C (NS), after BR 0.92 (0.13)°C (^*P<0.05), after WI80 0.96 (0.13)°C^*, and after WI20 1.03 (0.09)°C^*. All responded similarly to exercise: they decreased (NS) by 0.5–0.7°C in minutes 4–8 and equilibrated at +0.1 to +0.5°C at 60–70. Skin heat conductance was not different among the five conditions (range = 147–159 kJ·m^–2·h^–1·°C^–1). Results from an intercorrelation matrix suggested that total body sweat rate was more closely related toT _re at 70 min (T _re70) than limb sweat rate or blood flow. Only 36% of the variability inT _re70 could be accounted for by total sweating, and less than 10% from total body dehydration. It would appear that multiple factors are involved which may include change in sensitivity of thermo- and osmoreceptors.     

Effect of pyridostigmine on the exercise-heat response of man

Summary The effect of pyridostigmine on thermoregulatory responses was evaluated during exercise and heat stress. Eight heat acclimated, young adult male subjects received four doses of pyridostigmine (30 mg) or identical placebo tablets every 8 h, in a double blind, randomized, cross-over trial. A 30.3%, SD 4.6% inhibition of the circulating cholinesterase (ChE) activity was induced in the pyridostigmine-treated group. The subjects were exposed to 170-min exercise and heat-stress (dry bulb temperature, 33° C; relative humidity 60%) consisting of 60 min in a sitting position and two bouts of 50-min walking (1.39 m · s^–1, 5% gradient) which were separated by 10-min rest periods. No differences were found between treatments in the physiological responses and heat balance parameters at the end of exposure: heart rate (f _c) was 141 beats · min^–1, SD 16 and 150 beats · min^–1, SD 12, rectal temperature (T _re) was 38.5°C, SD 0.4° and 38.6°C, SD 0.3°, heat storage was 60 W · m^–2, SD 16 and 59 W · m^–2, SD 15 and sweat rate was 678 g · h^–1, SD 184 and 661 g · h^–1, SD 133, in the pyridostigmine and placebo treatments, respectively. The changes in T _re and f _c over the heat-exercise period were parallel in both study and control groups. Pyridostigmine caused a slight slowing of f _c (5 beats·min^–1) which was consistent throughout the entire exposure (P<0.001) but was of no clinical significance. The overall change in f_c was similar for both groups. We have concluded that pyridostigmine administration, in a dose sufficient to induce a moderate degree of ChE inhibition, does not significantly affect performance of exercise in the heat.     

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.     

Influence of the menstrual cycle and oral contraceptives on thermoregulatory responses to exercise in young women

Summary Thermoregulatory responses to exercise in relation to the phase of the menstrual cycle were studied in ten women taking oral contraceptives (P) and in ten women not taking oral contraceptives (NP). Each subject was tested for maximal aerobic capacity ( ) and for 50% exercise in the follicular (F) and luteal (L) phases of the menstrual cycle. Since the oral contraceptives would have prevented ovulation a quasi-follicular phase (q-F) and a quasi-luteal phase (q-L) of the menstrual cycle were assumed for P subjects. Exercise was performed on a cycle ergometer at an ambient temperature of 24° C and relative air humidity of 50%. Rectal (T _re), mean skin ( ), mean body ( ) temperatures and heart rate (f _c) were measured. Sweat rate was estimated by the continuous measurement of relative humidity of air in a ventilated capsule placed on the chest, converted to absolute pressure (PH₂O_chest). Gain for sweating was calculated as a ratio of increase inPH₂O_chest to the appropriate increase inT _re for the whole period of sweating (G) and for unsteady-state (G_u) separately. The did not differ either between the groups of subjects or between the phases of the menstrual cycle. In P, rectal temperature threshold for sweating (T _{re, td}) was 37.85° C in q-L and 37.60° C in q-F (P < 0.01) and corresponded to a significant difference fromT _re at rest. TheT _re, andf _c increased similarly during exercise in q-F and q-L. No menstrual phase-related differences were observed either in the dynamics of sweating or in G. In NP,T _{re, td} was shorter in L than in F (37.70 vs 37.47° C,P<0.02) with a significantly greater value fromT _re at rest. The dynamics and G for sweating were also greater in L than in F. The G_u was 36.8 versus 16.6 kPa · ° C^–1 (P<0.01) while G was 6.4 versus 3.8 kPa · ° C^–1 (P<0.05), respectively. TheT _re, andf _c increased significantly more in phase F than in phase L. It was concluded that in these women performing moderate exercise, there was a greater temperature threshold and larger gains for sweating in phase L than in phase F. Intake of oral contraceptives reduced the differences in the gains for sweating making the thermoregulatory responses to exercise more uniform.     

Evaluation of a temperate-environment test of heat tolerance in prior heatstroke patients and controls

Summary It has been reported that scores from a temperate-environment step test describe the heat-tolerance status of prior heatstroke patients (HP). This investigation evaluated the ability of this temperate-environment heat-tolerance test (HTT) to indicate altered heart rate (HR) and rectal temperature (T _re )responses of HP, after 7 days of heat acclimation. On day 1, ten male HP (61 ± 7 days post-heatstroke) and five control subjects (C) bench-stepped (0.30 m high, 27 steps · min^–1) for 15 min (25.8° C dry bulb, 16.2° C wet bulb). On days 2–8, subjects underwent heat acclimation (40.1° C dry bulb, 23.8°C wet bulb; treadmill, 90 min · day^–1). Heat acclimation resulted in significant decreases in final HR (152±5 vs 130±3 beats·min^–1 P<0.025) and finalT _re (38.62±0.11 vs 38.13±0.07°C,p < 0.01) in HP. One HP but no C was defined heat intolerant, exhibiting inability to adapt to daily exercise in the heat. On day 9, HP repeated HTT, exactly as performed on day 1; mean group HTT scores did not change (day 1=39±6; day 9=48±6,P>0.05). All physical characteristics and physiological responses of HP (days 1, 2, 7, 9) were statistically similar (P>0.05) to those of C. In contrast to heat-acclimation data, HTT scores (score 30) indicated that four HP were heat intolerant on day 1 and two HP were heat intolerant on day 9. It was concluded that HTT was not a substitute for lengthier tests of heat tolerance conducted in hot environments, because HTT scores (at 25.8°C did not reflect HR andT _re responses (at 40.1° C) in 33% of heat-acclimated (e.g., heat-tolerant) HP. In addition, HTT scores did not validly discriminate between heat tolerant and heat-intolerant HP.     

Control of heat-induced cutaneous vasodilatation in relation to age

Summary Well matched unacclimatised older (age 55–68, 4 women, 2 men) and younger (age 19–30, 4 women, 2 men) subjects performed 75 min cycle exercise (40% ) in a hot environment (37°C, 60% rh). Rectal temperature (T _re), mean skin temperature (¯T _sk), arm blood flow (ABF, strain gauge plethysmography), and cardiac output (Q, CO₂ rebreathing) were measured to examine age-related differences in heat-induced vasodilatation.T _re and¯T _sk rose to the same extent in each group during the exposure. There was no significant intergroup difference in sweat rate (older: 332±43 ml · m^–2 · h^–1, younger: 435±49 ml · m^–2 · h^–1; mean±SEM). However, the older subjects responded to exercise in the heat with a lower ABF response which could be attributed to a lower for the same exercise intensity. The slope of the ABF-T _re relationship was attenuated in the older subjects (9.3±1.3 vs 17.9±3.3 ml · 100 ml^–1 · min^–1 · °C^–1,p <0.05), but theT _re threshold for vasodilatation was about 37.0°C for both groups. These results suggest an altered control of skin vasodilatation during exercise in the heat in older individuals. This attenuated ABF response appears to be unrelated to , and may reflect an age-related change in thermoregulatory cardiovascular function.     

The effects of warming by active and passive means on the subsequent responses to cold water immersion

Two experiments were undertaken to investigate the effects of warming the body upon the responses during a subsequent cold water immersion (CWI). In both experiments the subjects, wearing swimming costumes, undertook two 45-min CWIs in water at 15° C. In experiment 1, 12 subjects exercised on a cycle ergometer until their rectal temperatures (T _re) rose by an average of 0.73°C. They were then immediately immersed in the cold water. Before their other CWI they rested seated on a cycle ergometer (control condition). In experiment 2, 16 different subjects were immersed in a hot bath (40° C) until their T _re rose by an average of 0.9° C; they were then immediately immersed in the cold water. Before their other CWI they were immersed in thermoneutral water (35° C; control condition). Heart rate in both experiments and respiratory frequency in experiment 1 were significantly (P < 0.05) higher during the first 30 s of CWI following active warming. In experiment 1, the rate of fall of T _re during the final 15 min of CWI was significantly (P < 0.01) faster when CWI followed active warming (2.46° C · h^–1) compared with the control condition (1.68°C · h^–1). However, this rate was observed when absolute T _re was still above that seen in the control CWIs. It is possible, therefore, that if longer CWIs had been undertaken, the two temperature curves may have converged and thereafter fallen at similar rates; this was the case with the aural temperature (T _au) seen in experiment 1 and the T _au and T _re in experiment 2. It is concluded that pre-warming is neither beneficial nor detrimental to survival prospects during a subsequent CWI.     

Thermal tolerance following artificially induced polycythaemia

Polycythaemia has been shown to improve physical performance, possibly due to increased arterial oxygen transport. Enhanced thermoregulatory function may also accompany this manipulation, since a greater proportion of the cardiac output becomes available for heat dissipation. We further examined this possibility in five trained men, who participated in three-phase heat stress trials (20 min rest, 20 min cycling at 30% peak power W_peak and 20 min at 45% W_peak at 38.3 (SEM 0.7)°C [relative humidity 41.4 (SEM 2.9)%]. Trials were performed during normocythaemia (control) and polycythaemia, obtained by reinfusion of autologous red blood cells and resulting in significant elevation of arterial oxygen transport. During the polycythaemic trials, the subjects demonstrated diminished thermal strain, as evidenced by a significant reduction in cardiac frequency (f _c: 12 beats · min^–1 lower throughout the test;P < 0.05), and reduced auditory canal temperatures (T _ae) during the latter 20-min phase (P < 0.05). Forearm sweat onset was more rapid (363.0 compared to 1083.0 s;P < 0.05), and forearm sweat rate (. _msw) sensitivity was elevated from 1.80 to 2.91 · mg · cm^–2 · min^–1 · °C^–1 (P < 0.05). Foreheadm _sw was depressed during the final 20 min, while forearmm _sw was greater during all test phases, averaging 0.94 and 1.20 mg · cm^–2 · min^–1, respectively, over the 60 min. Skin blood flows for the upper back, upper arm and forearm were reduced (P < 0.05). Polycythaemia enhanced thermoregulation, through an elevation in forearm sweat sensitivity and.m _sw, but not via increased cutaneous blood flow. These modifications occurred simultaneously with decreases inf _c andT _ae, resulting in greater thermal tolerance.     

Forearm temperature profile during the transient phase of thermal stress

Summary The transient temperature response of the resting human forearm immersed in water at temperatures (T _w) ranging from 15 to 36°C was investigated. Tissue temperature (T _t) was continuously monitored by a calibrated multicouple probe during the 3-h immersions.T _t was measured every 5 mm, from the longitudinal axis of the forearm to the skin surface. Skin temperature, rectal temperature, and blood flow ( ) were also measured during the immersions. The maximum rate of change of the forearm mean tissue temperature ( ) occurred during the first 5 min of the immersion. was linearly dependent onT _w (P<0.001), with mean values (SEM) ranging from –0.8 (0.1) °C · min^–1 at 15°C to 0.2 (0.1) °C · min^–1 at 36°C. The maximum rate of change of compartment mean temperature was dependent (P<0.001) on the radial distance from the longitudinal axis of the forearm. The half-time for thermal steady state of the forearm mean tissue temperature was linearly dependent onT _w between 30 and 36°C (P<0.01), with mean values (SEM) ranging from 15.6 (0.6) min at 30°C to 9.7 (1.2) min at 36°C and not different between 15 and 30°C, averaging 16.2 (0.6) min. There was a significant linear relationship between the half-time for thermal steady-state of the compartment mean temperature and the radial distance from the longitudinal axis of the forearm for each value ofT _w tested (P<0.001). The data of the present study suggest that the forearm is an important determinant of the transient thermal response of the forearm tissue during thermal stress.     

Comparison in men of physiological responses to exercise of increasing intensity at low and moderate ambient temperatures

Summary In six male subjects the sweating thresholds, heart rate (f _c, as well as the metabolic responses to exercise of different intensities [40%, 60% and 80% maximal oxygen uptake (VO_2max)], were compared at ambient temperatures (T _a) of 5° C (LT) and 24° C (MT). Each period of exercise was preceded by a rest period at the same temperature. In LT experiments, the subjects rested until shivering occurred and in MT experiments the rest period was made to be of exactly equivalent length. Oxygen uptake (VO₂) at the end of each rest period was higher in LT than MT (P< 0.05). During 20-min exercise at 40%VO_2max performed in the cold no sweating was recorded, while at higher exercise intensities sweating occurred at similar rectal temperatures (T _re) but at lower mean skin (T _sk) and mean body temperatures (T _b) in LT than MT experiments (P<0.001). The exercise inducedVO₂ increase was greater only at the end of the light (40%VO_2max) exercise in the cold in comparison with MT (P<0.001). Bothf _c and blood lactate concentration [la]_b were lower at the end of LT than MT for moderate (60%VO_2max) and heavy (80%VO_2max) exercises. It was concluded that the sweating threshold during exercise in the cold environment had shifted towards lower (T _b) andT _sk. It was also found that subjects exposed to cold possessed a potentially greater ability to exercise at moderate and high intensities than those at 24° C since the increases inT _re,f _c and [la]_b were lower at the lowerT _a.     

Comparison of two cool vests on heat-strain reduction while wearing a firefighting ensemble

This study evaluated the effectiveness of a six-pack versus a four-pack cool vest in reducing heat strain in men dressed in firefighting ensemble, while resting and exercising in a warm/humid environment [34.4°C (day bulb), 28.9°C (wet bulb)]. Male volunteers (n = 12) were monitored for rectal temperature (T _re), mean skin temperature (T _sk), heart rate, and energy expenditure during three test trials: control (no cool vest), four-pack vest, and six-pack vest. The cool vests were worn under the firefighting ensemble and over Navy dungarees. The protocol consisted of two cycles of 30 min seated rest and 30 min walking on a motorized treadmill (1.12 m · s^–1, 0% grade). Tolerance time for the control trial (93 min) was significantly less than both vest trials (120 min). Throughout heat exposure, energy expenditure varied during rest and exercise, but no differences existed among all trials (P > 0.05). During the first 60 min of heat exposure, physiological responses were similar for the four-pack and six-pack vests. However, during the second 60 min of heat exposure the six-pack vest had a greater impact on reducing heat strain than the four-pack vest. PeakT _e andT _sk at the end of heat exposure for 6-pack vest [mean (SD) 38.0(0.3)°C and 36.8(0.7)°C] were significantly lower compared to four-pack [38.6 (0.4)°C and 38.1(0.5)°C] and controls [38.9(0.5)°C and 38.4(0.5)°C]. Our findings suggest that the six-pack vest is more effective than the four-pack vest at reducing heat strain and improves performance of personnel wearing a firefighting ensemble.     

Does feeding regime affect physiologic and thermal responses during exposure to 8, 20, and 27° C?

Summary When the loss of body heat is accelerated by exposure to low environmental temperatures, additional substrates must be oxidized to provide energy to sustain temperature homeostasis. Therefore, the present investigation examined the relation between feeding regime [pre-experimental carbohydrate feeding (FED) vs a fast (FAST)], during 120 min of exposure to 8, 20, and 27° C in well-nourished men. The following were examined: tissue insulation (I; °C · m² · W^–1), rectal temperature (T _re; °C), and oxygen consumption ( O₂; ml · kg^–1 · min^–1). O₂, T _re, and I revealed no significant differences between treatments (FED vs FAST) at any temperature. At 27° C, I was less (P < 0.05) than at 20 and 8° C, and decreased (P < 0.05) as exposure time increased. At 8° C, O₂was higher (P < 0.5) than at 20 or 27°C, and O₂increased as time increased (P < 0.05). T _re decreased (P < 0.05) as time increased for all conditions. Respiratory exchange ratio (R) differed (P < 0.05) between treatments (FED vs FAST), temperature (8 vs 20° C), and across time. Values for R suggests that carbohydrate accounted for 56% and 33% of caloric utilization during the FED vs FAST conditions, respectively. At 8 vs 20° C, R represented 54% vs 30% of cabohydrate utilization. Across time, R demonstrated that in both conditions (FED vs FAST) there was a decreased reliance on carbohydrate utilization for energy provision. From these data it appears that while substrate utilization differed between dietary treatment and across time this did not differentially affect O₂or T _re during protracted exposure to 8, 20, and 27° C. The higher R in the 8° C condition for both dietary treatments demonstrates that carbohydrate utilization is increased in shivering cold-exposed humans. However, the reduction in R across time suggests that fat oxidation is also involved in metabolic heat production and core temperature maintenance during shivering in the cold.     

A comparison of human thermoregulatory response following dynamic exercise and warm-water immersion

We tested the hypothesis that the prolonged elevated plateau of esophageal temperature (T _es) following moderate exercise is a function of some exercise-related factors and not the increase in heat content andT _es during exercise, by comparing the response to increaseT _es during exercise (endogenous heating) and warm-water immersion (exogenous heating). Nine healthy, young [24.0 (1.9) years] subjects performed two separate experiments: (1) 15 min of treadmill exercise at 70% and 15 min rest in a climatic chamber at 29°C, followed by 15 min of immersion in a 42°C water bath and a further 60 min of recovery in the climatic chamber [exercise-water (EW)]; and (2) 15 min of immersion in a 42°C water bath followed by 60 min of recovery in the climatic chamber [water-only (WO)]. Esophageal (T _es) and skin (T _sk) temperatures were recorded at 5-s intervals throughout. TheT _ea at which the forearm to finger temperature gradient (T _fa-T _fi) abruptly decreases was used to identify the threshold for forearm cutaneous vessel dilation (Th_dil) during exercise. Pre-exerciseT _es values were 36.64°C and 36.74°C for EW and WO respectively. The EW post-exerciseT _ea value fell to a stable level of 37.12°C and this value differed by 0.48°C (P < 0.05) from baseline, but was similar to Th_dil (37.09°C). Despite a 1.2°C increase inT _es during the subsequent warm-water immersion,T _es returned to the post-exercise value (37.11°C). The WO post-immersionT _es fell to a stable plateau of 36.9°C, which was not statistically different from the pre-immersion T_es. The data for both warm-water treatments support the hypothesis that increases inT _es and heat content alone are not the primary mechanisms for the post-exercise elevation inT _es and Th_dil. These data also support our previous observation that the exercise-induced elevation in Th_dil persists into recovery.     

Effect of heat stress on muscle blood flow during dynamic handgrip exercise

Summary During exercise in a hot environment, blood flow in the exercising muscles may be reduced in favour of the cutaneous circulation. The aim of our study was to examine whether an acute heat exposure (65–70°C) in sauna conditions reduces the blood flow in forearm muscles during handgrip exercise in comparison to tests at thermoneutrality (25° C). Nine healthy men performed dynamic handgrip exercise of the right hand by rhythmically squeezing a water-filled rubber tube at 13% (light), and at 34% (moderate) of maximal voluntary contraction. The left arm served as a control. The muscle blood flow was estimated as the difference in plethysmographic blood flow between the exercising and the control forearm. Skin blood flow was estimated by laser Doppler flowmetry in both forearms. Oesophageal temperature averaged 36.92 (SEM 0.08) ° C at thermo-neutrality, and 37.74 (SEM 0.07) ° C (P<0.01) at the end of the heat stress. The corresponding values for heart rate were 58 (SEM 2) and 99 (SEM 5) beats -min^–1 (P<0.01), respectively. At 25° C, handgrip exercise increased blood flow in the exercising forearm above the control forarm by 6.0 (SEM 0.8) ml · 100 ml^–1 · min^–1 during light exercise, and by 17.9 (SEM 2.5) ml · 100 ml^–1 · min^–1 during moderate exercise. In the heat, the increases were significantly higher: 12.5 (SEM 2:2) ml · 100 ml^–1 · min^–1 at the light exercise level (P<0.01), and 32.2 (SEM 5.9) ml · 100 ml^–1·min^–1 (P<0.05) at the moderate exercise level. Skin blood flow was not significantly different in any of the test conditions between the two forearms. These results suggested that hyperthermia of the observed magnitude did not reduce blood flow in active muscles during light or moderate levels of dynamic handgrip exercise.     

Differences in rectal temperatures measured at depths of 4–19 cm from the anal sphincter during exercise and rest

The purpose of the present study was to examine the discrepancies in rectal temperature (T _re) at various depths. Nineteen young males performed two bouts of bicycle exercise and recovery. T _re was simultaneously measured at depth of 4, 6, 8, 10, 13, 16, and 19 cm, alongside the measurement of skin temperatures. We found small but statistically significant differences by depth in the absolute T _re, the magnitude of rise in T _re and the lag of response in T _re. During the stabilization stage before exercise, T _re at 4 cm-depth was 0.5°C lower than T _re at 16 cm-depth (p < 0.05). As the depth measured in the rectum was shallower, the rise in T _re during exercise was greater. However the rise in T _re at 10, 13, 16 and 19 cm showed no systemic difference. Among seven depths, T _re at 16 cm-depth had the most stable feature with the longest latent period (3.1 ± 1.3 min) and the smallest rise (0.8 ± 0.3°C), while T _re at 4 cm-depth was the most responsive to the change of exercise and rest with the shortest latent period (1.0 ± 0.6 min) and the greatest rise (1.2 ± 0.5°C). The differences observed in the depths from 4 to 19 cm were offset by exercise to some extent. In summary, T _re appeared in different manners according to the seven depths during the repetition of exercise and rest, but T _re deeper than 10 cm-depth seemed to have no systematic differences.     

Regulation of local sweating in sleep-deprived exercising humans

Summary Thermoregulatory sweating [total body (m _sw,b), chest (m _sw,c) and thigh (m _sw,t) sweating], body temperatures [oesophageal (T _oes) and mean skin temperature (T _sk)] and heart rate were investigated in five sleep-deprived subjects (kept awake for 27 h) while exercising on a cycle (45 min at approximately 50% maximal oxygen consumption) in moderate heat (T _air andT _wall at 35° C. Them _sw,c andm _sw,t were measured under local thermal clamp (T _sk,1), set at 35.5° C. After sleep deprivation, neither the levels of body temperatures (T _oes,T _sk) nor the levels ofm _{sw, b},m _{sw, c} orm _{sw, t} differed from control at rest or during exercise steady state. During the transient phase of exercise (whenT _sk andT _sk,1 were unvarying), them _{sw, c} andm _{sw, t} changes were positively correlated with those ofT _oes. The slopes of them _{sw, c} versusT _oes, orm _{sw, t} versusT _oes relationships remained unchanged between control and sleep-loss experiments. Thus the slopes of the local sweating versusT _oes, relationships (m _{sw, c} andm _{sw, t} sweating data pooled which reached 1.05 (SEM 0.14) mg·cm^–2·min^–1°C^–1 and 1.14 (SEM 0.18) mg·cm^–2·min^–1·°C^–1 before and after sleep deprivation) respectively did not differ. However, in our experiment, sleep deprivation significantly increased theT _oes threshold for the onset of bothm _{sw, c} andm _{sw, t} (+0.3° C,P<0.001). From our investigations it would seem that the delayed core temperature for sweating onset in sleep-deprived humans, while exercising moderately in the heat, is likely to have been due to alterations occurring at the central level.     

Gender differences in physiological reactions to thermal stress

Following an extensive anthropometric evaluation, thermoregulatory responses were studied in nine men and nine women who performed immersed exercise with post-exercise rest in 28°C water. During the post-exercise period esophageal temperature (T _es), oxygen consumption, heat flux and skin blood perfusion were monitored at 10s intervals, with average minute values used for calculations. The T _es (relative to restingT _es) at which sweating abated and shivering commenced were defined as the T _es thresholds for the cessation of sweating and onset of shivering, respectively. No significant gender differences were evident in the sweating and shivering threshold T _es values, or the magnitude of the null-zone. Usingz-tests for parallelism the rates of core cooling across the null-zone were not found to differ significantly between genders, nor were the slopes of the perfusion: T _es responses across the null-zone or the post-threshold shivering responses (ml·kg^–1·min^–1·°C^–1). The slope of the sweating response (measured from immersion until sweat cessation; g·m^–2·min^–1°C^–1) was, however, significantly lower in the female than in the male samples (z = 3.93;P < 0.01). Despite the gender-related dimorphic distribution of adipose tissue, both men and women lost equal proportions of their total heat flux from central and peripheral measurement sites. Performing a standardized regression using the rate of core cooling across the null-zone as the dependent variable and gender as a dummy variable, gender and adipose tissue mass were not found to be significant factors in determining the rate of core cooling, while mass ( = 1.73;P < 0.05) and muscle mass ( = 1.86;P < 0.05) did contribute significantly to the rate of core cooling. It was concluded that, except for the quantitative differences in the sweating response, men and women respond to deviations in core temperature in a similar manner, with mass and muscle mass modifying this response.     

Perception of effort during high-intensity exercise at low,moderate and high wet bulb globe temperatures

The purpose of this study was to determine the effect of low, moderate and high wet bulb globe temperatures (T _wbg) on cardiovascular variables and ratings of perceived exertion (RPE) during moderately prolonged, high-intensity exercise. Six subjects [four men and two women; mean (SD) age, 22.0 (1.2) years; maximum oxygen consumption ({ie519-1}), 51.0 (8.4) ml · kg^–1 · min^–1] completed 30 min of exercise (80% {ie519-2}) on a cycle ergometer at low [14.7 (2.1)°C], moderate [21.0 (1.5)° C], and high [27.4 (2.3)° C]T _wbg. Two additional subjects completed 20 min of exercise in the high temperature condition, but completed 30 min in the moderate and lowT _wbg. Heart rate (f _c), blood pressure, blood lactate (La), mean skin temperature ( _sk), , and RPE were measured at 10, 20 and 30 min. Results showed thatf _c, rate pressure product, RPE, pulmonary ventilation and ventilatory equivalent for oxygen increased (P < 0.05) across time for all conditions, while decreased across time. _sk andf _c were significantly greater across time in the high condition [35.9 (0.65)° C; 176 (12.6) beats · min^–1] compared to the moderate [34.6 (1.5)° C; 170 (17.2) beats · min^–1] and the low condition [31.7 (1.5)° C; 164 (17.1) beats-min^–1]. However, there were no differences throughout exercise in RPE [high,.16.2 (2.0); moderate, 16.4 (2.2); low, 16.3 (1.9)] and across the conditions. These data suggest that RPE is closely related to metabolic intensity but is not a valid indicator of cardiovascular strain during exercise in highT _wbg conditions.     

Thermoregulatory responses of prepubertal boys and young men in changing temperature linearly from 28 to 15°C

To examine thermoregulatory responses of prepubertal children to cold stress, 11 boys (aged 8 years) and 11 young men (aged 19–23 years), wearing only trunks, participated in this study. They sat in air at 28°C for 30 min (equilibrium period) and then in conditions where air temperature (T _a) was decreased linearly from 28 to 15°C (at a constant rate of 0.22°C · min^–1) for 60 min, at a fixed relative humidity of 65%. In the equilibrium period there was no significant difference between the groups for rectal temperature [T _re, mean 37.30 (SEM 0.10) and mean 37.43 (SEM 0.14)°C in the boys and the men, respectively] or for the respective skin temperatures (except for the forehead), but metabolic heat production ( ) was significantly greater for the boys [mean 57.1 (SEM 1.2) and mean 52.0 (SEM 0.9)W. m^–2,P <0.005]. With decliningT _a, the skin temperatures decreased in both groups (P <0.001), but the decrease was significantly greater for the boys (P < 0.05), especially on the limbs as represented by the thigh and forearm. No significant correlations were observed between the limb skin temperatures compared to surface area-to-mass ratio or limb skinfold thicknesses in either group. The rate of increase in asT _a decreased was significantly lower for the boys (P < 0.01) largely because of a higher before the cold exposure. Thus, the mean during the cold exposure did not differ between the groups [mean 63.6 (SEM 1.1) and mean 61.6 (SEM 1.1) W · m^–2 in boys and men, respectively]. When theT _a was lowered,T _re in the boys started falling (P < 0.001), whereas theT _re in the young men did not change for 60 min. TheT _re during the 60-min exposure was significantly lower (P < 0.001) for the boys [mean 37.01 (SEM 0.13) and mean 37.48 (SEM 0.18)°C at the end of the exposure]. It was concluded that whenT _a was lowered, the prepubertal boys appeared to vasoconstrict more in their limbs and to be somewhat more hypothermic, compared to the young men.     

Melatonin has no effect on tolerance to uncompensable heat stress in man

This study examined whether a 5 mg dose of melatonin induced a lower rectal temperature (T _re) response at rest in both a cool and hot environment while wearing normal military combat clothing, and then examined the influence of this response on tolerance to exercise in the heat while wearing protective clothing. Nine men performed four randomly ordered trials involving 2 h of rest at ambient temperatures of either 23 °C or 40 °C followed by exercise at an ambient temperature of 40 °C. The double-blind ingestion of placebo or melatonin occurred after 30 min of rest. The mean T _re during rest at 23 °C had decreased significantly from 36.8 (SD 0.1) °C to 36.7 (SD 0.2) °C at 90 min following the ingestion of the drug, whereas values during the placebo trial did not change. The lower T _re response during the melatonin trial remained during the first 50 min of exercise in the heat while wearing the protective clothing. Since the final mean T _re at the end of exercise also was significantly reduced for the melatonin [39.0 (SD 0.4) °C] compared with the placebo [mean 39.1 (SD 0.3) °C] trial, tolerance times approximated 95 min in both conditions. During rest at 40 °C, melatonin did not affect the mean T _re response which increased significantly during the last 90 min from 36.9 (SD 0.1) °C to 37.3 (SD 0.1) °C. This increase in T _re during the rest period prior to donning the protective clothing decreased tolerance time approximately 30 min compared with the trials that had involved rest at 23 °C. Total heat storage summated over the rest and exercise periods was not different among the trials at 15 kJ · kg⁻¹. It was concluded that the small decrease in T _re following the ingestion of 5 mg of melatonin at rest in a cool environment had no influence on subsequent tolerance during uncompensable heat stress. Accepted: 26 June 2000