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Biomedical subjects

J C Sagot

Publications and source records attributed to J C Sagot.

12 recordsLinked to original sources
PubMed1988

Thermal and circulatory responses during prolonged exercise at different levels of hydration.

After a control experiment under initial normal hydration (N), five healthy unacclimated subjects were studied to investigate the effects of initial hypo- and hyperhydration on cardiovascular and thermo-regulatory responses to prolonged intermittent exercise in the heat (To = 36 degrees C; Tdp = 10 degrees C; Va = 0.6 m.s-1). Prior hydrohydration (O) was obtained by diuretics and prior hyperhydration (R) by ingestion of 0.5 L of isotonic (ISO) electrolyte sucrose solution 30 min before the experiments (4 h) started. Exercise (70 W) lasted 3 hours, and was periodically interrupted by resting periods (5-10 min). Three dehydration (D) runs were thus performed under the three initial hydration states (O,N,R) without fluid replacement during the exercise period. Four additional rehydration runs were carried out: 2 in each initial hydration level (O, R) included ingestion (at 36 degrees C) of water or ISO-solution during the first 3 hours. Physiological measurements were continuously recorded and hourly blood samples (15 ml) were obtained. Results showed that dehydration increased core temperature and heart rate and provoked blood hypovolemia and hyperosmolarity, the latter being somewhat prevented by prior ISO-ingestion. Dehydration reduced significantly the overall sweat rate only in hypohydrated subjects and the large hyperosmolarity seemed to be responsible for this. The significant Tcore rise during dehydration is unlikely to be the result of a decrease in evaporative heat transfer, which was found only in the case of initial hypohydration. Rehydration during exercise with water or ISO-solution induced different dynamic responses depending on the initial hydration level, but it never restored plasma volume.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1988

Local sweating responses of different body areas in dehydration-hydration experiments.

Five subjects performed intermittent exercise on a bicycle ergometer (25 min work, 5 min rest cycles for 2 hours, and 20 min work, 10 min rest cycles for a further hour) in a hot environment (air and wall temperatures = 36 degrees C; dew-point temperature = 10 degrees C; air velocity = 0.6 m.s-1). The relative mechanical work load was of 70 W (30% of the maximal aerobic capacity). Seven experimental tests were carried out in order to induce a plasma hypovolemia associated with either a plasma hypo- or hyperosmolarity. The preexercise level of body hydration was also manipulated by giving a diuretic, or by ingestion of 500 ml of isotonic electrolyte sucrose solution before the start of exercise. Continuous measurements were made of rectal and mean skin temperatures. The sweating responses of the chest and of the thigh (over the active muscles of the leg) were monitored from 4 sweat collection capsules highly ventilated. On each of these body areas, the local skin temperatures under one of the 2 capsules was kept at a constant level (37 degrees C). The effects of the level of body hydration on the sweating response only appear when a high local thermal clamp is imposed beneath the capsule. This local effect is particularly strong over the active muscles of the thigh. The influence of the preexercise hydration appears during dehydration tests. This effect is not significant when fluid is given to the subject during the exercise. The change in the sensitivity of the thermoregulatory system is more strongly associated with plasma osmolarity than hypovolemia.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1987

Sweating responses and body temperatures during nocturnal sleep in humans.

The changes in the central control of sweating were investigated in five sleeping subjects under neutral and warm conditions [operative temperature (To) = 30, 33, and 34 degrees C; dew-point temperature = 10 degrees C]. Esophageal (Tes) and mean skin (Tsk) temperatures, chest sweat rate (msw,1), and concomitant electroencephalographic data were recorded. Throughout the night, msw,1 was measured under a local thermal clamp of 38 degrees C. Results showed that the thermal environment exerted a strong influence on both the levels and the time patterns of body temperatures. Moreover, local sweating rate correlated positively with Tes, and this relationship varied according to sleep stages. For a given Tes level, there was a sleep stage-related gradation in msw,1 that was higher in slow-wave sleep (SWS) than in stage 1-2 and the lowest in rapid-eye-movement (REM) sleep. This is explained by a change in the excitability or the sensitivity of the thermoregulatory system. The msw,1 differences between stage 1-2 and SWS are accounted for by a decrease in the Tes threshold (Tset) for sweating while the slope of the msw,1-Tes relation remains unchanged. The lower msw,1 in REM sleep is explained by a lesser slope for the msw,1-Tes relation without any Tset change from stage 1-2.

Adult↗
PubMed1986

Hydration during exercise. Effects on thermal and cardiovascular adjustments.

Five young unacclimatised subjects were exposed for 4 h at 34 degrees C (10 degrees C dew-point temperature and 0.6 m X s-1 air velocity), while exercising on a bicycle ergometer: 25 min work--5 min rest cycles for 2 hours followed by 20 min work--10 min rest cycles for two further hours. 5 experimental sessions were carried out: one without rehydration (NO FLUID) resulting in 3.1% mean loss of body weight (delta Mb), and four sessions with 20 degrees C fluid ingestion of spring water (WATER), hypotonic (HYPO), isotonic (ISO) and hypertonic (HYPER) solutions to study the effects of fluid osmolarity on rehydration. Mean final rehydration (+/- SE) after fluid intake was 82.2% (+/- 1.2). Heart rate was higher in NO FLUID while no difference among conditions was found in either delta Mb or hourly sweat rates. Sweating sensitivity was lowest in the dehydration condition, and highest in the WATER one. Modifications in plasma volume and osmolarity demonstrated that NO FLUID induced hyperosmotic hypovolemia, ISO rehydration rapidly led to plasma isoosmotic hypervolemia, while WATER led to slightly hypoosmotic normovolemia. It is concluded that adequate rehydration through ingestion of isotonic electrolyte-sucrose solution, although in quantities much smaller than evaporative heat loss, rapidly restored and expanded plasma volume. While osmolarity influenced sweating sensitivity, the plasma volume changes (delta PV) within the range -6% less than or equal to delta PV + 4% had little effect on temperature adjustments in our conditions.

Adult↗
PubMed1986

Temperature regulation during intermittent exercise with progressive dehydration.

Effects of dehydration (3% of initial body weight) on temperature regulation were investigated in 5 men during intermittent exercise of 4 h duration at a dry air temperature of 34 degrees C. Relative mechanical work load was 50% of the subject's steady state heart rate, which was 170 beats . min-1. During rehydration from the 70th min to the end of the exercise, the subjects drank, every 10 min in equal portions, an amount of water (20 degrees C) totaling up to 80% of the body weight loss recorded during dehydration runs. Continuous measurements were made of rectal (Tre) and mean skin (Tsk) temperatures and of whole body weight loss. Chest sweating rate (msw) was measured from a capsule located under a local thermal clamp (36 degrees C). Blood samples were obtained during rest periods and after the 1st and the 4th hour of exercise. Compared to dehydration runs, water intake did not always cause an increase of msw while body temperatures always decreased. Dehydration resulted in a decrease in plasma volume and in increases of plasma osmolality, [Na+] and [K+]. Water intake induced a thermoregulatory response whose intensity largely differs from one body area to another. The change in the slope of the relation of msw to Tre features a decrease in the sensitivity of the thermoregulatory system with dehydration. The whole body water loss is significantly correlated with the change in plasma volume and body temperatures (Tre, Tsk). This suggests that the reduced sweating response observed during dehydration can be related to plasma hypovolemia.

Adult↗
PubMed1986

Sweat gland response to local heating during sleep in man.

In order to assess whether the fluctuations in the sweating response occurring during sleep are related to changes in central drive or in peripheral sweat gland reactivity, 4 healthy male subjects spent 6 non-consecutive nights in a climatic chamber. Air temperature was 25 degrees C, dew-point temperature was 10 degrees C and air velocity was 0.3 m X s-1, while wall temperature was either 38 degrees C, 46 degrees C or 48.7 degrees C giving 3 levels of operative temperature (To = 30, 33 or 34 degrees C). During the whole night, 2 local sweating rates on the right and the left sides of the upper chest were continuously recorded from 12 cm2 area capsules using a dew-point hygrometer technique, while applying local thermal clamps, a constant 2 degrees C difference in local skin temperatures being imposed between the two symmetrical skin areas. Continuous measurements were made of rectal temperature, 10 local skin temperatures, 2 EEGs, 2 EOGs, 1 EMG and 1 ECG. Results show that the multiplicative relationship between the peripheral influence of local skin temperature and the central drive for sweating described in waking subjects, is still valid in sleeping subjects. No peripheral change appears in sweat gland reactivity between the different sleep stages. Changes in the sensitivity of the thermoregulatory system occurring during sleep cannot be explained by a local factor acting at the sweat gland level.

Body Temperature Regulation↗
PubMed1984

Contribution of skin thermal sensitivities of large body areas to sweating response.

The thermal sensitivity of different parts of the body was investigated by heating large areas of the body surface while the mean skin temperature calculated from Hardy and DuBois ' formula (1938) was always kept constant. The right arm sweating responses recorded under a local thermal clamp were related to changes in segmental skin temperatures of the different parts of the body. The results show that: 1) the various local peripheral signals are projected into integrating structures in the central nervous system; 2) the thermal sensitivity is greater for the head-and-trunk area in comparison with other parts of the body. For resting nude subjects, the formula of Hardy and DuBois remains a pertinent way for evaluating the role of skin thermal signals in the central drive for sweating. The peripheral contribution to the central sweating drive depends only on the skin temperature change and on the size of the stimulated area.

Adult↗
PubMed1983

Oral temperature as an index of core temperature during heat transients.

Rectal (Tre), oral (Tor) and oesophageal (Tes) temperatures were measured in five exercising subjects exposed for two hours to five conditions (1) a steady condition (WR) involving a constant work load (50 W) at a constant air temperature (Ta = 36.5 degrees C); (2) air temperature variations (delta Ta) between 28 degrees C and 45 degrees C and (3) between 23 degrees C and 50 degrees C at constant work load (50 W); (4) and (5) to work load variations (delta W) between 25 W and 75 W at a constant Ta (= 36.5 degrees C). Oral temperature recordings were taken sublingually and were either continuous or discontinuous. When discontinuous, the time needed for Tor to stabilize after the mouth opening was taken into account. The respective reliability of Tor and Tre as estimates of Tes were compared in each condition. Results showed that the resting (Tor - Tes) difference (+ 0.12 degrees C) was barely modified after two hours of exposure, whereas Tre overestimated Tes by 0.2 degrees C to 0.4 degrees C depending on the condition. The Tor variations were highly correlated with Tes variations under steady condition and under air temperature variations. In these conditions, Tor represented the best estimate of Tes. Under work-load variations, Tor was less closely related to Tes than was Tre. It is suggested that the relative inertia of Tor to step changes in exercise intensity could be ascribed to work induced variations in mouth blood flow.

Adult↗
PubMed1982

Impedance of the lower respiratory system in ducks measured by forced oscillations during normal breathing.

The lower respiratory system of 10 conscious Pekin ducks breathing normally was subjected to superimposed oscillations of 1.3 to 16 Hz by a small volume piston pump. Induced sinusoidal flow (VO) and pressure (PO) signals were measured in late expiration, when the gas flow ventilated by the animal was minimum. The modulus of the respiratory impedance was calculated as the ratio PO/VO. The values obtained at the various oscillatory frequencies were compared to those predicted on the basis of a series mechanical network model consisting of resistive, inertial and compliant elements (RIC) using a least squares non linear regression method. The experimental data fitted well the frequency response of a simple RIC mathematical model. After correcting for the effects of the endotracheal tube, the mean values +/- SE of the optimized parameters were: resistance 4.8 +/- 0.4 cm H2O . L-1 . sec; inertance: 0.05 +/- 0.01 cm H2O . L-1 . sec2; compliance: 7.7 +/- 0.5 ml . cm H2O-1; natural frequency: 8.0 +/- 0.4 Hz. It is concluded that: (1) the lower respiratory system in ducks can be closely modeled by a RIC mechanical series network model; (2) the forced oscillation method can be used to investigate avian mechanics of breathing, with the birds awake and breathing spontaneously.

Airway Resistance↗
PubMed1982

Respiratory mechanics of Pekin ducks under four conditions: pressure breathing, anesthesia, paralysis or breathing CO2-enriched gas.

Impedance magnitude (Z) of the lower respiratory system was studied in Pekin ducks, using forced oscillations of a small volume at the airways opening in the range 1.6-16 Hz. The experiments were performed on 5 awake ducks enclosed in a body plethysmograph and spontaneously breathing ambient air at a transrespiratory pressure (Prs, the pressure difference between the lung and the body surface) which was varied in steps from -10 cm H2O (compression) to +10 cm H2O (distension). In 3 anesthetized birds, the effects of CO2 breathing and muscular paralysis were also studied. Analysis of end-expiratory Z data yielded estimates of respiratory resistance (R), inertance (I) and compliance (C). During positive or negative pressure breathing in conscious ducks, minute volume (V) and end-tidal CO2 (PETCO2) remained unchanged from normal (Prs = zero) while tidal volume (VT) and ventilatory period (Ttot) decreased. The respiratory system in late expiration can be modelled well with a simple series R-I-C mechanical model at Prs values of zero, +10 and -10 cm H2O. The value of Z increased at all frequencies studied during compression of the respiratory system (Prs = -10 cm H2O) and did not change much from normal (Prs = zero) during distension (Prs = +10 cm H2O). Both resistance and inertance increased during compression. During distension contradictory changes in resistance and inertance suggest that complex changes in flow profile and/or in flow pathways occurred with positive pressure breathing. Anesthesia or paralysis did not noticeably change the oscillatory resistance or inertance, but increased oscillatory compliance. CO2-breathing did not affect the respiratory impedance in late expiration, but reduced its flow dependence along the ventilatory cycle.

Airway Resistance↗
PubMed1982

Thermophysiological responses to humid heat: sex differences.

1. Thermophysiological responses of four men and four pre- and postovulatory women were compared in humid heat conditions. Responses of pre- and postovulatory women are similar except for body temperature levels, which were significantly higher after ovulation. 2. Pronounced sex-related differences were observed in sweating rate and in body temperature variations. For the same evaporation, the sweat rate in men was higher than in women; as a consequence of this, the dripping rate was larger in men and thus the sweat decline was more important. Body temperature increases were larger in men in function of time and therefore temperature regulation in women was considered to be more efficient.

Adult↗