Effects of wearing two different types of clothing on body temperatures during and after exercise

The experiment was conducted to investigate the human thermoregulatory responses during rest, exercise and recovery atT _a 20°C and 60% R.H. under the conditions of wearing two different types of clothing. Six healthy men wore two types of clothing: one covering the whole body area except the head (Type A, weight 1656 g), and the other covering only the trunk, upper arms and thighs (Type B, weight 996 g). The level of rectal temperature was kept significantly higher in Type B than in Type A during rest and recovery. The increased and decreased rates of rectal temperature during exercise and recovery were significantly greater in Type A than in Type B, respectively. These findings are discussed from the viewpoint of the differences of skin temperatures of the extremities between Type A and Type B.     

Muscle temperature and muscle metabolism during short-term exercise in the goat

1. 1.|External heat exchangers acting on lower aortal blood temperature were used to dissociate hindleg muscle temperature (T_hlm) from general internal temperature (T_int) during short-term exercise of moderate intensity.

2. 2.|In series 1 39°C T_hlm was combined with 40.6°C T_int, and in series II 42°C T_hlm was combined with 39.8°C T_int.

3. 3.|At constant work rates, the 3°C difference in muscle temperature did not result in significantly different concentrations of muscle metabolites.

4. 4.|It is concluded that high local muscle temperature without general hyperthermia does not influence muscle metabolism during short-term moderate excercise.

Climate and physiological heat strain during exercise

A body-atmosphere energy exchange model (BIODEX) using heat transfer theory and empirical relationships is described which predicts the change in body core temperature during exercise as an index of thermal strain. Index values may be interpreted as the length of the period of activity before the heat load on the body causes internal body temperature to rise to critical levels. The performance of the model tested under controlled laboratory conditions using human subjects was found to be reliable. BIODEX is used to show the thermal significance of midsummer climatic conditions in New Zealand for those jogging out-doors.     

A comparison of sweating responses during exercise and recovery in terms of sweating rate and body temperature

Based on the hypothesis that the relation between sweating rate and body temperature should be different during exercise and rest after exercise, we compared the sweating response during exercise and recovery at a similar body temperature. Healthy male subjects performed submaximal exercise (Experiment 1) and maximal exercise (Experiment 2) in a room at 27° C and 35% relative humidity. During exercise and recovery of 20 min after exercise, esophageal temperature (Tes), mean skin temperature, mean body temperature ( ), chest sweating rate ( ), and the frequency of sweat expulsion (F _SW) were measured. In both experiments, andF _SW were clearly higher during exercise than recovery at a similar body temperature (Tes, ). was similar during exercise and recovery, or a little less during the former, at a similarF _SW. It is concluded that the sweating rate during exercise is greater than that during recovery at the same body temperature, due to greater central sudomotor activity during exercise. The difference between the two values is thought to be related to non-thermal factors and the rate of change in mean skin temperature.     

Respiratory heat loss and core temperatures during submaximal exercise

1. 1. This study examined the effect of inhaling air supersaturated with water on changes of core temperatures in submaximally exercising males.

2. 2. During exercise with inhalation of supersaturated relative to low-air-humidity air, a significant elevation in tympanic temperature (P = 0.009) and a significant decrease in esophageal temperature (P = 0.004) were observed.

3. 3. Forehead skin temperatures significantly decreased during humidified air inhalation (P = 0.02) supporting that this treatment induced greater thermolytic responses that cooled the skin.

4. 4. The results are consistent with the conclusion that heat loss from the upper airways directly influenced human cerebral temperatures as indexed by tympanic temperatures.

     

Effect of high air and soil temperature on dry matter production,pod yield and yield components of groundnut

Groundnuts (Arachis hypogaea L.) grown in the semi-arid tropics are commonly exposed to air and soil temperatures above 35 °C during the reproductive period causing significant yield losses. The objectives of this study were to determine: (i) whether effects of high air and/or high soil temperature in two contrasting cultivars were similar; (ii) the effects of the timing of imposition of high air and soil temperature; (iii) the effects of high air, high soil and both stresses combined on yield and yield components; and (iv) whether the effects of high air and high soil temperature were additive or multiplicative. Plants were grown at optimum and ambient soil temperature from planting until start of podding at 45 d after planting (DAP) in Experiment 1, and until start of flowering at 28 DAP in Experiment 2. Thereafter, plants of each cultivar were exposed to a factorial combination of two air temperatures (optimum: 28°/22 °C and high: 38°/22 °C) and two soil temperatures (ambient: 26°/24 °C and high: 38°/30 °C) until final harvest at 90 DAP. The effects of high air and high soil temperatures imposed from start of flowering or podding were similar. Exposure to high air and/or high soil temperature significantly reduced total dry matter production, partitioning of dry matter to pods, and pod yields in both the cultivars. High air temperature had no significant effect on total flower production but significantly reduced the proportion of flowers setting pegs (fruit-set) and hence fruit numbers. In contrast, high soil temperature significantly reduced flower production, the proportion of pegs forming pods and 100 seed weight. The effects of high air and soil temperature were mostly additive and without interaction. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effect of a low-carbohydrate diet on plasma and sweat ammonia concentrations during prolonged nonexhausting exercise

The purpose of this investigation was to examine the effect of low body glycogen stores on plasma ammonia concentration and sweat ammonia excretion during prolonged, nonexhausting exercise of moderate intensity. On two occasions seven healthy untrained men pedalled on a cycle ergometer for 60 min at 50% of their predetermined maximal O₂ uptakes ( _max) firstly, following 3 days on a normal mixed diet (N-diet) (60% carbohydrates, 25% fat and 15% protein) and secondly, following 3 days on a low-carbohydrate diet (LC-diet) (less than 5% carbohydrates, 50% fat and 45% protein) of equal energy content. Blood was collected from the antecubital vein immediately before, at 30th and at 60th min of exercise. Sweat was collected from the hypogastric region using gauze pads. It was shown that plasma ammonia concentrations after the LC-diet were higher than after the N-diet at both the 30th and 60th min of exercise. Sweat ammonia concentration and total ammonia loss through the sweat were also higher after the LC-diet. The higher ammonia concentrations in plasma and sweat after the LC-diet would seem to indicate an increased ammonia production, which may be related to reduced initial carbohydrate stores.     

Effects of acute exercise on serum interleukin-17 concentrations in hot and neutral environments in trained males

The purpose of this study was to determine the effects of acute exercise on IL-17 concentrations in hot and neutral environments in trained males. Ten trained, non-heat acclimated males performed two 1 h run on treadmill at 60% VO2max in neutral (22±1 °C, 50±5RH) and hot (35±1 °C, 50±5) temperature conditions. Samples of the venous blood were taken (Pre, post, 2 h post) for determination of serum IL-17, cortisol concentrations and numbers of leukocytes and neutrophils. In addition, body temperature, RPE and PVC during exercise were measured. The collected data were analyzed using the Repeated-Measures analyses of variance and Bonferroni post hoc and Paird T tests (p<0.05). The concentration of cortisol and total number of leukocytes increased significantly after exercise, in both conditions (p<0.0001) and were significantly higher in hot than neutral (p=0.016, p=0.002). During the rest period (2 h post) the number of neutrophils increased significantly in hot environment (p=0.018). The concentrations of IL-17 increased significantly only after exercise in hot (p<0.0001) and were significantly higher during hot than neutral (p=0.002). The results suggest that exercise in hot environment cause increase in body temperature, perceived exertion and cardiac-vascular changes which are sufficient to elicit immune, hormonal and inflammatory responses. The present results confirm the additive effect of heat stress on the IL-17 response during exercise.     

Preferred temperature of the elderly after cold and heat exposures determined by individual self-selection of air temperature

1. 1. The purpose of the study was to investigate the preferred temperature of the elderly after cold and heat exposures.

2. 2. Eight elderly and 9 young females wearing the same type of clothing were exposed to cold (10°C), moderate (25°C) or hot (35°C) environments for 30 min in the exposure room.

3. 3. Then they moved to the self-control room in which the temperature was set at 25°C, and the room temperature increased or decreased continuously by 0.4°C every minute.

4. 4. The subjects were instructed to operate the switch when they felt uncomfortably warm or cool during a 90-min period.

5. 5. In operating the switch, the changing in room temperature shifted to the opposite direction.

6. 6. The ambient temperature was recorded continuously and analyzed as the preferred temperature, which was defined as the midpoint temperature of the crest and trough of temperature records.

7. 7. The preferred temperatures after the cold exposure were significantly higher than those of other exposure conditions in the elderly.

8. 8. On the other hand, in the young, there was no significant difference in the preferred temperature among the exposure conditions.

9. 9. Although the effect of exposure to cold or hot environments decreased in the latter parts of self-control, the elderly still preferred the higher temperature after cold exposure.

The comparison between cool and warm-hot environments on lipolytic response during prolonged exercise

The purpose of this study was to investigate the effect of cool exposure on lipolytic response during prolonged intermediate-intensity exercise in humans. Eight male subjects participated in this study; they performed 120-min cycle ergometer exercise at 60% of maximal oxygen uptake (VO2max) in a climatic chamber at 10 degrees C (C) and 30 degrees C (WH). There were no significant differences in oxygen uptake and respiratory exchange ratio between the two conditions during the prolonged exercise. Significant influences of cool exposure were observed in the changes in both heart rate and rectal temperature (p<0.01). Although cool exposure had no significant effects on plasma triglyceride, free fatty acid, and glycerol levels, changes in adrenaline and noradrenaline levels at C were significantly lower than WH during the prolonged exercise (p<0.01). Changes in the ratio of glycerol to noradrenaline (Gly/Nad), as an index of lipolytic efficiency, were significantly high at C as compared with WH (p<0.01). These results suggest that cool exposure has an influence on lipid metabolism during prolonged intermediate-intensity exercise, from the viewpoint of efficiency in lipolysis.     

Heat induced fatigue and changes of the EEG is not related to reduced perfusion of the brain during prolonged exercise in humans

(1) Exercise-induced hyperthermia is associated with a gradual slowing of the electroencephalogram (EEG), an increase in perceived exertion (RPE) and a lowering of the cerebral perfusion.

(2) During exercise EEG changes were linearly correlated to core temperature (r²=0.67; P<0.05) and RPE (r² =0.54, P<0.05), but manipulation of cerebral perfusion by voluntary breathing efforts and by CO₂ inhalation did not alter RPE or EEG.

(3) In conclusion EEG changes with hyperthermic exercise are not a simple effect of the reduced cerebral perfusion but may relate to the fatigue that arises concomitantly with the increases in core and brain temperatures.     

Energetics of calling and metabolic substrate use during prolonged exercise in the European treefrog Hyla arborea

Rates of oxygen consumption and carbon dioxide release were measured in calling and resting European tree frogs using open-flow-through respirometry. The energetic cost of calling was high with an average of 1.076 ml O₂/(g · h) at average call rates of 8000 calls/h. The maximum factorial metabolic scopes averaged 24 with momentary peak values ranging between 5 and 41. There was a threefold difference in O₂-consumption between individual males calling at the same rate. Respiratory quotients indicated that both lipids and carbohydrates were used to fuel calling. Carbohydrates provided the major fuel (69% on average) with dependence on carbohydrates increasing with call rate. In contrast to marathon runners, there was no shift in metabolic substrate use over a calling period of 2–3 h. Accepted: 25 September 2000     

The effect of root temperature on rose plants in relation to air temperature

Rose plants (Rosa hybrida ‘Sonia’=‘Sweet Promise’) were grown in heated (minimum night temperature 17°C), and unheated greenhouses with or without root heating to 21°C. These trials covered 6 growth cycles extending over two winter seasons. In the heated greenhouse, root heating did not increase yield, flower quality or plant development. In the unheated greenhouse, root-heated plants grew as well as those in the air-heated greenhouse as long as the air temperature did not fall below 6°C. When minimum night temperatures fell below 6°C, growth, yield and quality were reduced, irrespective of root temperature. Daytime plant water relations were studied in plants growing at 6 different root temperatures in the unheated greenhouse. Leaf resistance to water diffusion was lowest at optimal root temperature. Total leaf water potential was not significantly affected by root temperature.     

Relationship between ventilatory response and body temperature during prolonged submaximal exercise.

We examined whether an increase in skin temperature or the rate of increase in core body temperature influences the relationship between minute ventilation (Ve) and core temperature during prolonged exercise in the heat. Thirteen subjects exercised for 60 min on a cycle ergometer at 50% of peak oxygen uptake while wearing a suit perfused with water at 10 degrees C (T10), 35 degrees C (T35), or 45 degrees C (T45). During the exercise, esophageal temperature (Tes), skin temperature, heart rate (HR), Ve, tidal volume, respiratory frequency (f), respiratory gases, blood pressure (BP), and blood lactate were all measured. We found that oxygen uptake, carbon dioxide output, BP, and blood lactate did not differ among the sessions. Tes, HR, Ve, and f remained nearly constant from minute 10 onward in the T10 session, but all of these parameters progressively increased in the T35 and T45 sessions, and significantly higher levels were seen in the T45 than the T35 session. For all but two subjects in the T35 and T45 sessions, plotting Ve as a function of Tes revealed no threshold for hyperventilation; instead, increases in Ve were linearly related to Tes, and there were no significant differences in the slopes or intercepts between the T35 and T45 sessions. Thus, during prolonged submaximal exercise in the heat, Ve increases with core temperature, and the influences of skin temperature and the rate of increase in Tes on the relationship between Ve and Tes are apparently small.     

Salivary and serum cortisol levels during recovery from intense exercise and prolonged,moderate exercise

The aim of this study was to compare serum (SERc) and salivary cortisol (SALc) responses during recovery from two different exhaustive exercises to determine peak cortisol sampling time and the agreement between SERc and SALc levels. Twelve healthy men underwent a maximal treadmill graded exercise to exhaustion (MEx) and a prolonged, submaximal cycle exercise in the heat for 90 min (PEx) while SERc and SALc samples were taken in parallel at baseline, end of exercise, and 15 min intervals over one hour of recovery. MEx and PEx significantly increased SERc and SALc levels (p < 0.01) while absolute SERc levels were approximately 7-10 folds higher than SALc. SERc and SALc showed highly positive correlation (R = 0.667-0.910, p < 0.05) at most sampling times and only a few individual values were out of 95% limit of agreement when analyzed by Bland-Altman plots. However, peak SERc levels (MEx: 784.0±147, PEx: 705.5±212.0 nmol · L⁻¹) occurred at 15 min of recovery, whereas peak SALc levels (MEx: 102.7±46.4, PEx: 95.7±40.9 nmol · L⁻¹) were achieved at the end of exercise in MEx and PEx. The recovery trend of SERc and SALc also differed following MEx and PEx. Activity of 11β-hydroxysteroid dehydrogenase type 2 enzymes may be suppressed following MEx compared to PEx. In conclusion, sampling for peak SERc and SALc levels should take into account their evolution and clearance characteristics as well as type of exercise performed, whereas SALc appeared to be a more sensitive marker than SERc for the measurement of cortisol responses during exercise recovery.     

The role of pulmonary CO2 flow in the control of the phase i ventilatory response to exercise in humans

To gain an insight into the origin of the phase I ventilatory response to exercise (ph I) in humans, pulmonary ventilation WE) and end-tidal partial pressures of oxygen and carbon dioxide (P _ETO₂ and P _ETCO₂, respectively) were measured breath-by-breath in six male subjects during constant-intensity exercise on the cycle ergometer at 50, 100 and 150 W, with eupnoeic normocapnia (N) or hyperpnoeic hypocapnia (H) established prior to the exercise test. Cardiac output (Q₂) was also determined beat-by-beat by impedance cardiography on eight subjects during moderate exercise (50 W), and the C0₂ flow to the lungs (Q₂·C_vCO₂ where C_vCO₂ is concentration of CO₂ in mixed veneous blood) was estimated with a time resolution of one breathing cycle. In N, the initial abrupt increase of PE during ph I (V_E approximately 18 l · min^–1 above rest) was followed by a transient fall. When P _ETCO₂ started to increase (and P _ETO₂ decreased) V_E increased again (phase II ventilatory response, ph II). In H, during ph I V_E was similar to that of N. By contrast, during ph II V_E kept gradually decreasing and started to increase only when P _ETCO₂ had returned to approximately 40 mmHg (5.3 kPa). Thus, as a result of the prevailing initial conditions (N or H) a temporal shift of the time-course of V_E during ph II became apparent. No correlation was found between C0₂ flow to the lungs and V_E during ph I. These results are interpreted as suggesting that an increased C0₂ flow to the lungs does not constitute an important factor for the initial hyperventilatory response to exercise. They are rather compatible with a neural origin of ph I, and would support the neurohumoral theory of ventilatory control during exercise.     

Effects of estrus cycle on thermoregulatory responses during exercise in rats

In female rats, rectal temperature (Tre), tail vasomotor response, oxygen uptake (VO2), and carbon dioxide production (VCO2) were measured in proestrus and estrus stages during treadmill running at two different speeds at an ambient temperature (Ta) of 24 degrees C. Experiments were performed at 2.00-6.00 a.m., when the difference in Tre was greatest between the two stages; Tre at rest in the estrus stage was 0.54 degrees C higher than in the proestrus stage. In a mild warm environment, threshold Tre for a rise in tail skin temperature (Ttail) was also higher in the estrus stage than in the proestrus stage. In contrast, no difference was seen in the threshold Tre and steady state Tre at the end of exercise between proestrus and estrus stages. These values were higher at the higher work intensity. VO2 was also similar between the two stages, except in the second 5 min after the beginning of exercise, when VO2 was greater and Tre rose more steeply in the proestrus stage. These data indicate that deep body temperature during exercise is regulated at a certain level depending on the work intensity and is not influenced by the estrus cycle.     

Core temperature response to cycling exercise: Effect of time of day and measurement site

This study evaluated the effect of time of day and temperature measurement site on core temperature response to exercise. Six trained cyclists performed a 1 h cycling exercise at a fixed power-output of 160 W in a controlled environment (ambient temperature of 21.5±1.6 °C and relative humidity of 31±6%) at batyphase +2 h (08:00 h) and acrophase +2 h (20:00 h) of their estimated circadian temperature rhythm; corresponding respectively to the heat gain and heat loss mode phases. Throughout the exercise, rectal and gastro-intestinal temperature data were collected. A two-way ANOVA was applied and a common nonlinear logistic-type function dependant on three parameters (asymptote, xmid and scale) was used to fit collected data. ANOVA only indicated a time of day effect without interaction with exercise duration. A nonlinear mixed-effect model allowed further analysis of temperature kinetics. The model indicated a higher theoretical increase in temperature at the end of morning exercise compared to the evening session. However, the circadian difference observed at rest persists throughout the exercise. Theoretical asymptotic temperature values at the end of the exercise and scale values (inversely proportional to the slope) are higher for the rectal measurement site than for the gastro-intestinal measurement. The model proposed offers a solution for refining the study of individual core temperature response to prolonged exercise. The main advantage is that it takes into consideration intra- and inter-individual variability in temperature kinetics.     

Cheek skin temperature and thermal resistance in active and inactive individuals during exposure to cold wind

1. The present study examined the effect of the thermal state of the body (as reflected by rectal temperature) on cheek skin temperature and thermal resistance in active and inactive subjects.

2. Active subjects were exposed to a 30 min conditioning period (CP) (0 °C air with a 2 m/s wind), followed immediately by a 30 min experimental period (EP) (0 °C with a 5 m/s wind). Inactive subjects were exposed to a 30 min CP (22 °C air with no wind), followed immediately by a 45 min EP (0 °C air with a 4.5 m/s wind). The CP period was used to establish a core temperature difference between the active and inactive subjects prior to the start of EP. The 0 °C exposure was replaced with a −10 °C ambient air exposure and the experiment was repeated on a separate day. Subjects were comfortably dressed for each ambient condition.

3. Cheek skin temperature was not significantly higher in active subjects when compared to inactive subjects, but thermal resistance was higher in active subjects.

4. Cheek skin temperature and thermal resistance both decreased as ambient temperature decreased from 0 to −10 °C. The lower cheek thermal resistance at −10 °C may have been due to a greater cheek blood flow as a result of cold-induced vasodilation.