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Biomedical subjects

I B Mekjavic

Publications and source records attributed to I B Mekjavic.

At least 19 recordsLinked to original sources

Temperature dependence of habituation of the initial responses to cold-water immersion.

The initial responses to cold-water immersion, evoked by stimulation of peripheral cold receptors, include tachycardia, a reflex inspiratory gasp and uncontrollable hyperventilation. When immersed naked, the maximum responses are initiated in water at 10 degrees C, with smaller responses being observed following immersion in water at 15 degrees C. Habituation of the initial responses can be achieved following repeated immersions, but the specificity of this response with regard to water temperature is not known. Thirteen healthy male volunteers were divided into a control (C) group (n = 5) and a habituation (H) group (n = 8). Each subject undertook two 3-min head-out immersions in water at 10 degrees C wearing swimming trunks. These immersions took place at a corresponding time of day with 4 days separating the two immersions. In the intervening period the C group were not exposed to cold water, while the H group undertook another six, 3-min, head-out immersions in water at 15 degrees C. Respiratory rate (fR), inspiratory minute volume (VI) and heart rate (fH) were measured continuously throughout each immersion. Following repeated immersions in water at 15 degrees C, the fR, VI and fH responses of the H group over the first 30 s of immersion were reduced (P < 0.01) from 33.3 breaths x min(-1), 50.5 l x min(-1) and 114 beats x min(-1) respectively, to 19.8 breaths x min(-1) 26.41 x min(-1) and 98 beats x min(-1), respectively. In water at 10 degrees C these responses were reduced (P < 0.01) from 47.3 breaths x min(-1), 67.61 x min(-1) and 128 beats x min(-1) to 24.0 breaths x min(-1), 29.5 l x min(-1) and 109 beats x min(-1), respectively over a corresponding period of immersion. Similar reductions were observed during the last 2.5 min of immersions. The initial responses of the C group were unchanged. It is concluded that habituation of the cold shock response can be achieved by immersion in warmer water than that for which protection is required. This suggests that repeated submaximal stimulation of the cutaneous cold receptors is sufficient to attenuate the responses to more maximal stimulation.

Adaptation, Physiological

Substrate utilisation during exercise and shivering.

It is generally assumed that exercise and shivering are analogous processes with regard to substrate utilisation and that, as a consequence, exercise can be used as a model for shivering. In the present study, substrate utilisation during exercise and shivering at the same oxygen consumption (VO2) were compared. Following an overnight fast, eight male subjects undertook a 2-h immersion in cold water, designed to evoke three different intensities of shivering. At least 1 week later they undertook a 2-h period of bicycle ergometry during which the exercise intensity was varied to match the VO2 recorded during shivering. During both activities hepatic glucose output (HGO), the rate of glucose utilisation (Rd), blood glucose, plasma insulin, free fatty acid (FFA) and beta-hydroxybutyrate (B-HBA) concentrations were measured. The VO2 measured during the different levels of shivering averaged 0.49 l.min-1 (level 1: low), 0.6 l.min-1 (level 2: low-moderate), and 0.9 l.min-1 (level 3: moderate), and corresponded closely to the levels measured during exercise. HGO and Rd were greater (P < 0.05) during exercise than during shivering at the same VO2 (9.5% and 14.7%, respectively). The average (SD). HGO during level 3 exercise was 3.0 (0.91) mg.kg-1.min-1 compared to 2.76 (1.0) mg.kg-1.min-1 during shivering. The values for Rd were 3.06 (0.98) mg.kg-1.min-1 during level 3 exercise and 2.68 (0.82) mg.kg-1.min-1 during shivering. Blood glucose levels did not differ between conditions averaging 5.4 (0.3) mmol.l-1 over all levels of shivering and 5.2 (0.3) mmol.l-1 during exercise. Plasma FFA and B-HBA were higher (P < 0.01) during shivering than during corresponding exercise (12.3% and 33.3%, respectively). FFA averaged 0.61 (0.2) mmol.l-1 over all levels of shivering and 0.47 (0.16) mmol.l-1 during exercise. The figures for L-HBA were 0.44 (0.13) mmol. l-1 during all levels of shivering and 0.32 (0.1) mmol.l-1 during exercise. Plasma insulin was higher (P < 0.05) during level 2 and 3 shivering compared to corresponding exercise; at these levels the average value for plasma insulin was 95.9 (21.9) pmol.l-1 during shivering and 80.6 (16.1) pmol.l-1 during exercise. On the basis of the present findings it is concluded that, with regard to substrate utilisation, shivering and exercise of up to 2 h duration should not be regarded as analogous processes.

3-Hydroxybutyric Acid

Thermoregulatory responses of circum-pubertal children.

Passive temperature lability of nine circum-pubertal children [11.4 (1.2) years] was compared to that of nine young adult males [26.6 (5.2) years]. Each subject completed a 20-min period of exercise, followed immediately by post-exercise immersion in water at 28 degrees C. The aim of the exercise protocol was to induce a steady rate of sweating (Esw) while the postexercise immersion period induced cooling of the core region (tympanic temperature: Tty). The Tty values (relative to rest, delta Tty) at which sweating abated and at which shivering commenced were defined as the thresholds for the cessation of sweating and onset of shivering, respectively. While there was no significant difference between the delta Tty sweating thresholds, the onset of shivering, as reflected in the oxygen uptake (VO2) response, occurred at significantly higher (P < 0.05) delta Tty values in the children [mean (SD): - 0.07 (0.07) degrees C] than in the adults [ -0.22 (0.10) degrees C]. The slope of the Esw/delta Tty relationship was found to be significantly lower in the children (z = -5.64; P < 0.05), while the slopes of the VO2/delta Tty relationship were not significantly different (z = -0.84; P > 0.05). Skin blood perfusion was measured at the forehead (SkBP), and the slope of the SkBP/delta Tty relationship across the null-zone was significantly less in the children than in the adults (z = -2.13; P < 0.05) with the greatest reduction in perfusion occurring prior to the offset of sweating in the children. The subjective ratings of thermal comfort indicated that the children were more sensitive to changes in core temperature than the adults. It is concluded that maturation plays an important role in modifying thermoregulatory responses to deviations in core temperature. These results suggest that there may be differences in thermoregulatory "strategies" which are maturationally related.

Adolescent

Passive temperature lability in the elderly.

Thermoregulatory responses of nine healthy elderly [seven men and two women; mean age (SD) 73.9 (4.8) years] were compared to those of nine young adult men [26.6 (5.2) years]. They exercised on a cycle ergometer for 20 min at an intensity inducing a heart rate equivalent to 65% of their predicted maximum, and were thereafter immersed in 28 degrees C water. The exercise was conducted to elevate tympanic temperature (Tty) and initiate a steady rate of sweating. The post-exercise immersion period induced gradual cooling of Tty, and changes in Tty relative to resting levels (delta Tty) at which sweating abated and shivering commenced were defined as the delta Tty thresholds for the cessation of sweating (Tsw) and onset of shivering (Tsh), respectively. In addition to Tty, oxygen uptake (VO2; l.min-1), sweating rate (g.m-2.min-1), and forehead skin blood perfusion were also measured during the trials. The mean (SD) Tsw occurred at a significantly (P < 0.005) higher delta Tty [0.48 (0.18) degrees C] in the elderly than in the young adults [0.21 (0.06) degrees C], while the Tsh occurred at significantly (P < 0.005) lower delta Tty in the elderly [-0.64 (0.34) degrees C] than in young adults [-0.22 (0.10) degrees C]. Decreases in delta Tty below the shivering threshold were met with a significantly (P < 0.01) reduced VO2. The range of temperature lability between Tsw and Tsh, defined as the null-zone, was significantly greater in the elderly [1.12 (0.39) degrees C] than in the young adults [0.43 (0.12) degrees C], and the slope of the vasoconstrictor response in the null-zone was significantly (P < 0.001) lower in the elderly subjects. The present study demonstrates a greater passive core temperature lability in older individuals, since the effector responses of sweating and shivering were initiated at higher and lower levels of Tty, respectively. The magnitudes of the effector responses beyond the thresholds were also significantly reduced, suggesting that the elderly may be more susceptible to hypo-/hyperthermia during periods of endogenous and/or exogenous thermal stress.

Adult

Effects of blood-volume distribution on the characteristics of the carotid baroreflex in humans at rest and during exercise.

Seven supine subjects were studied at rest and during mild to moderate dynamic leg exercise with and without unloading of the cardiopulmonary baroreceptors accomplished by exposing the lower portion of the body to a subatmospheric pressure of 20 mmHg (Lower Body Negative Pressure, LBNP). The function of the cardiac branch of the carotid baroreflex was studied over its full operational range by measuring R-R intervals during application of pulse synchronous graded pressures (40 to -65 mmHg) in a neck-chamber device. Raising the carotid transmural pressure (systolic arterial pressure minus neck-chamber pressure) induced increasing R-R intervals in all conditions. In conformity with previous results from our laboratories it was found that the maximal rate of change in relative R-R intervals and the corresponding transmural pressure were higher during exercise than at rest, indicating that exercise increased the carotid baroreflex sensitivity and shifted its optimal buffering range to higher arterial pressures. LBNP did not affect the characteristics of the reflex at rest nor during exercise. It is concluded that reduced central venous pressure with consequent selective cardiopulmonary receptor disengagement exerts no influence on the carotid baroreflex control of heart rate (HR), as tested over the entire arterial pressure-effector response relation, either at rest or during mild-moderate exercise.

Adult

Autonomic nervous control of heart rate during blood-flow restricted exercise in man.

Power spectra of instantaneous heart rate (fc) allows the estimation of the contribution of sympathetic and parasympathetic control of fc during steady-state conditions. The present study was designed to examine autonomic control of fc as influenced by normal dynamic leg exercise and by ischemic leg exercise. Eight subjects performed supine cycle ergometry at 30% of their control peak work rate, with and without blood-flow restriction. Blood-flow restriction was induced by exposing the exercising legs to a supra-atmospheric pressure of 6.7 kPa (leg positive pressure; LPP). The exercise responses of arterial pressure and fc increased (P < 0.05) by LPP exposure. The exaggerated pressor response may be attributed to a chemoreflex drive originating in the ischemic muscles. Exposure to LPP during exercise also produced a significant decrease in parasympathetically mediated high frequency (HF; 0.15-1.00 Hz) fluctuation of fc, as indicated by a decrease (P < 0.05) in percent HF power compared to the control exercise level. During LPP exercise, the sympathetically mediated very low frequency (VLF; 0-0.05 Hz) fluctuation of fc increased, as indicated by an increase (P < 0.05) in percent VLF power above control exercise levels. Both LPP and control exercise conditions decreased (P < 0.05) power in all frequency ranges of interest compared to their respective resting conditions. The results suggest that the increase in fc associated with normal dynamic exercise was mediated predominantly by parasympathetic withdrawal, whereas the exaggerated fc response during ischemic exercise resulted from a combination of cardiac sympathetic drive and parasympathetic withdrawal.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult

Tear film bubble formation after decompression.

Decompression disorders can occur after a reduction in environmental pressure due to dissolved gases forming bubbles in affected tissues. The objective of this study was to evaluate the use of tear film bubble formation as an indicator of decompression. Eleven subjects were exposed to a simulated dive to 30.48 m (100 ft) (in sea water) for 15 min. There was a significant (p < 0.001) increase in tear film bubble formation post-dive. This noninvasive technique may be of value in both research and clinical environments for monitoring decompression.

Decompression Sickness

Characteristics of the carotid baroreflex in man during normal and flow-restricted exercise.

Eight subjects were studied in the supine position at rest, during normal dynamic leg exercise (control exercise) and with blood-flow restriction in the working legs (flow-restricted exercise). Graded muscle blood-flow restriction was accomplished by applying a supra-atmospheric pressure of 50 mmHg to the working legs. During incremental-load exercise, flow restriction reduced exercise performance and peak heart rate by 36% and 13%, respectively. The function of the cardiac branch of the carotid baroreflex was studied over its full operational range, at rest and during constant-load control and flow-restricted exercise, by measuring R-R intervals during application of pulse-synchronous graded pressures (40 to -65 mmHg) in a neck-chamber device. Heart rate and arterial pressure were higher during flow-restricted than control exercise, indicating that the flow restriction activated the muscle chemoreflex. Raising the carotid transmural pressure (systolic arterial pressure minus neck-chamber pressure) was accompanied by increasing R-R intervals in all conditions. The set point (point of baseline carotid transmural pressure and R-R interval) coincided with the midportion of the pressure-response curve at rest and with the threshold point of the curve during exercise. The maximal rate of change in relative R-R intervals and the corresponding carotid transmural pressure range were higher during control exercise than at rest and highest during flow-restricted exercise, indicating that exercise and especially flow-restricted exercise increased carotid baroflex sensitivity, and shifted the carotid baroreflex optimal buffering range to higher pressures. The results suggest that the carotid baroflex attenuates exercise heart rate increases mediated by the muscle chemoreflex and/or by central command.

Adult

Human temperature regulation during narcosis induced by inhalation of 30% nitrous oxide.

The study investigated the effect of inhalation of 30% nitrous oxide (N2O) on temperature regulation in humans. Seven male subjects were immersed to the neck in 28 degrees C water on two separate occasions. They exercised at a rate equivalent to 50% of their maximum work rate on an underwater cycle ergometer for 20 min and remained immersed for an additional 100 min after the exercise. In one trial (AIR) the subjects inspired compressed air, and in the other trial (N2O) they inspired a gas mixture containing N2O (20.93% O2-30% N2O-49.07% N2). Sweating, measured at the forehead, and shivering thermogenesis, as reflected by O2 uptake, were monitored throughout the 100-min recovery period. The threshold core temperatures at which sweating was extinguished and shivering was initiated were established relative to resting preexercise levels. Neither the magnitude of the sweating response nor the core threshold at which it was extinguished was significantly affected by the inhalation of N2O. In contrast, shivering thermogenesis was both significantly reduced during the N2O condition and initiated at significantly lower core temperatures [change in esophageal temperature (delta T(es)) = -0.98 +/- 0.33 degrees C and change in rectal temperature (delta T(re)) = -1.26 degrees C] during the N2O than during the AIR condition (delta T(es) = -0.36 +/- 0.31 degrees C and delta T(re) = -0.44 +/- 0.22 degrees C).(ABSTRACT TRUNCATED AT 250 WORDS)

Adult

Exercise breathing pattern during chronic altitude exposure.

Breathing pattern in response to maximal exercise was examined in four subjects during a 7-day acclimatisation to a simulated altitude of 4247 m (barometric pressure, PB = 59.5 kPa). Graded exercise tests to exhaustion were performed during normoxia (day 0), and on days 2 and 7 of hypoxia, respectively. Ventilation was significantly augmented in the hypoxic environment, as were both the mean inspiratory flow (VT/TI) and inspiratory duty cycle (TI/TTOT) components of it. VI/TI was increased due to a significant increase in tidal volume (VT) and a corresponding decrease in inspiratory time duration (TI). Throughout a range of exercise ventilation, TI/TTOT was increased due to an apparently greater decrease in expiratory time duration (TE) with respect to TI. In all cases, the relation between VT and TI displayed a typical range 2 behaviour, with evidence of a range 3 occurring at very high ventilatory rates. There was essentially no difference observed in the VT-TI relation during exercise between the normoxic and hypoxic conditions. No significant changes were observed in the breathing pattern in response to exercise within the exposure period (from day 2 to day 7), although there was a discernible tendency to a higher stage 3 plateau by day 7 of altitude exposure.

Acclimatization

The increased oxygen uptake upon immersion. The raised external pressure could be a causative factor.

The principal cause of the immediate transient elevation in ventilation (VE, L.min-1) and oxygen uptake (VO2, L.min-1), when a human subject is immersed in cold water is considered to be the stimulation of cutaneous cold receptors. The present study demonstrates that the initial VE and VO2 responses are comprised of a thermogenic and a hydrostatic component. The peak values in VE reached (mean +/- SD) 66.8 +/- 22.3, 53.9 +/- 38.1, 32.2 +/- 15.4, 22.5 +/- 3.6, 19.5 +/- 4.6 L.min-1 during the first minute of immersion in 10 degrees, 15 degrees, 20 degrees, 28 degrees and 40 degrees C water, respectively. Similarly, peaks (mean +/- SD) in VO2 of 1.22 +/- 0.25, 1.01 +/- 0.32, 0.98 +/- 0.39, 0.81 +/- 0.09, and 0.78 +/- 0.26 L.O2.min-1, were reached when subjects were immersed in 10 degrees, 15 degrees, 20 degrees, 28 degrees, and 40 degrees C water. It is concluded that the observed increases in VO2 during the first minute of immersion are partly due to the increased hydrostatic pressure causing a shift of venous blood towards the thoracic region, and a transient increase in the uptake of oxygen into the blood.

Body Temperature

Dynamic moisture permeation through clothing.

Dynamic moisture permeation through clothing often occurs during thermal transience, causing an imbalance between evaporative heat loss from the skin (Esk) and that from the clothing surface (Ecl). A device was designed to observe Esk and Ecl simultaneously. It consists of two relative humidity sensors coupled with thermistors so that densities of water vapor at two points within the boundary layer can be calculated. The rate of local evaporation is then estimated from Fick's law of diffusion. Local evaporation rates from the skin and clothing surface at the chest, arm, and thigh were measured during exposure to controlled ambient temperatures varying from 20 degrees-40 degrees C. The subjects wore four different types of helicopter pilot suits: Nomex/Neoprene, Goretex, cotton ventile, and Nomex/Insulite. For the Goretex and cotton ventile suits, consisting of relatively permeable and hygroscopic fabrics, a sudden increase in Esk, exponential decay of Esk, and a gradual increase in Ecl were observed. These appear to be associated with, respectively, the onset of sweat secretion, moisture build-up within the clothing, and water gain in the fabric. Thus, the device may be useful for observing dynamic moisture permeation through clothing.

Adult

The pattern of breathing during hypoxic exercise.

Breathing pattern was studied in six subjects in normoxia (FIO2 = 0.21) and hypoxia (FIO2 = 0.12) at rest and during incremental work-rate exercise. Ventilation (V) as well as mean inspiratory flow (VT/TI) increased with exercise intensity and were augmented in the hypoxic environment, whereas the ratio between inspiratory (TI) and total (Ttot) breath durations increased with exercise intensity but was unaffected by hypoxia. The relationship of tidal volume (VT) and inspiratory time duration (TI) showed linear, coinciding ranges for the normoxic and hypoxic conditions up to VT/TI values of about 2.5 1.s-1. At higher VT/TI values TI continued to decrease, whereas VT tended to level off, an effect which was more evident in the hypoxic condition. The results suggest that the hypoxic augmentation of exercise hyperpnea is primarily brought about by an enhancement of central inspiratory drive, the timing component being largely unaffected by the hypoxic environment, and that at low to moderate levels of exercise hyperpnea inspiratory off-switch mechanisms are essentially unaffected by moderate hypoxia.

Adult

Determining the rate of body heat storage by incorporating body composition.

The rate of body heat storage (S) is often used as an index of thermal stress. The traditional approach for determining S assumes that the specific heat (Cp) of all body tissues may be averaged to 0.83 kcal X kg-1 X degrees C-1, irrespective of the actual proportion of different tissues in the body. The present theoretical analysis primarily partitions the body into N compartments. However, this analytical approach involves the difficulty of making an exact evaluation of the mass and temperature of multiple compartments. Therefore, by adopting a two-compartment (core and shell) model, the specific heat capacities, mass fractions, and changes in the temperatures of the two compartments are combined, and S is defined as a function of adiposity (= mass fraction of peripheral tissues). Evaluation of a newly developed equation showed close agreement with observations during a series of cold-water immersion trials, and indicated that the new approach seems to adequately predict S as related to body composition.

Adult