The influence of environmental temperature upon the thermoregulatory responses to ethanol in man

1984 ◽  
Vol 66 (6) ◽  
pp. 733-739 ◽  
Author(s):  
I. W. Fellows ◽  
I. A. MacDonald ◽  
T. Bennett

1. Ten healthy male subjects ingested ethanol (BP; 0.5 g/kg body weight) after an overnight fast, on two separate occasions, at environmental temperatures of either 21°C or 3O°C. 2. The mean maximal fall in deep body temperature was not significantly different on the two occasions, being 0.18°C and 0.17°C respectively. 3. Metabolic rates throughout the experiments at the two temperatures were not significantly different. 4. The vasodilatation of the hand and forearm vascular beds after ethanol ingestion was markedly reduced at the lower environmental temperature. 5. In three subjects who ingested a higher dose of ethanol (BP; 1.0 g/kg body weight) after an overnight fast, at an environmental temperature of 2l°C, the mean maximum fall in core temperature was 0.15°C, which was not significantly different from the change seen after consumption of the lower dose of ethanol. 6. It is likely that the failure of ethanol ingestion to provoke hypothermia at the lower environmental temperature was due to the attenuated vasodilatation observed under these conditions.

1959 ◽  
Vol 19 (3) ◽  
pp. 232-240 ◽  
Author(s):  
S. A. BARNETT ◽  
ELIZABETH M. COLEMAN

SUMMARY Breeding stocks of mice of strain A2G have been studied at environmental temperatures of −3° and 21° C. The mean age of opening of the vagina was 33 days at −3° C, 26 days at 21° C. The mean body weight at opening was 13 g in both temperatures. The vaginal smear of typical oestrus appeared at a mean age of 61 days at −3° C, 38 days at 21° C; it was preceded by variable numbers of anomalous smears containing squamous cells. The mean length of the oestrous cycle was 8·5 days at −3° C, 4·8 days at 21° C. Females transferred from 21° to −3° C had longer cycles at first, but tended to return to normal after some months. The interval between parturitions had two modes, at about 3 and 6 weeks respectively: most intervals were around 6 weeks at −3° C, 3 weeks at 21° C. There was evidence of a negative correlation between the numbers weaned in successive parturitions, when the interval between parturitions was near the minimum. The slowing of the reproductive cycle at −3° C may be attributed to the prior demands of catabolism; but this does not account for the recovery of the mice transferred from warm to cold.


1992 ◽  
Vol 163 (1) ◽  
pp. 139-151 ◽  
Author(s):  
R. M. BEVAN ◽  
P. J. BUTLER

Six tufted ducks were trained to dive for food at summer temperatures (air, 26°C, water, 23°C) and at winter temperatures (air, 5.8°C, water 7.4°C). The mean resting oxygen consumption (Voo2) a t winter temperatures (rwin) was 90% higher than that at summer temperatures (Tsum), but deep body temperatures (Tb) were not significantly different. Diving behaviour and mean oxygen consumption for dives of mean duration were similar at Twin and at Tsum, although the mean oxygen consumption for surface intervals of mean duration was 50% greater at Twin and Tb was significantly lower (1°C) at the end of a series of dives in winter than it was in summer. There appears to be an energy saving of 67 J per dive during winter conditions and this may, at least partially, be the result of the metabolic heat produced by the active muscles being used to maintain body temperature. While at rest under winter conditions, this would be achieved by shivering thermogenesis. Thus, the energetic costs of foraging in tufted ducks in winter are not as great as might be expected from the almost doubling of metabolic rate in resting birds.


1993 ◽  
Vol 56 (2) ◽  
pp. 217-223 ◽  
Author(s):  
M. W. A. Verstegen ◽  
W. van der Hel ◽  
F. J. M. Pijls

AbstractHeat production, energy and nitrogen balances of artificially reared piglets from specific pathogen free sows, housed in a respiratory chamber, were measured over five successive periods of 7 days each from 4 to 39 days of age. The experiment was carried out at an environmental temperature decreasing from 33 to 27°C. The mean weight increased from 1·5 (at day 4) to 11·9 kg (at day 39). Daily rate of gain increased from about 100 g in periods 1 and 2 to 502 g per piglet in the fifth period.Daily protein deposition, as measured via nitrogen balance, increased from 17 to 96 g; fat deposition increased from about 0 to 100 g. Body composition at the start and end was determined by a comparative slaughter technique. Protein and fat content had a high correlation coefficient with body weight (R2 = 0·69 and 0·89, respectively). At birth these values were much lower, 0·24 and 0·01 for protein and fat, respectively.Nitrogen balance compared with slaughter technique led to an overestimation for protein deposition of proportionately 0·07. Fat gain measured from slaughter was proportionately 0·08 lower than that calculated from energy balance.Ratio of gain estimated from protein and fat gain with the balance technique relative to that measured ranged between 0·93 to 1·15 in various periods.


1959 ◽  
Vol 14 (5) ◽  
pp. 823-828 ◽  
Author(s):  
M. S. Malhotra ◽  
B. K. Sharma ◽  
R. Sivaraman

Data are presented on salt requirements in the tropics, based on observations on 24 acclimatized Indian subjects given diets containing 16.2, 11.2, 8.7, 6.2 and 3.1 gm of salt per day. Adequacy of salt diet was tested from the chloride excretion in urine and from the changes observed in thiocyanate space and plasma chloride concentration at the start and after the subjects had been on the restricted salt diet for a week. Sweat and chloride losses at different environmental temperatures were studied. The salt requirement of subjects walking for 2 hours in the sun at a speed of about 3.5 mph was found to be about 6.2 gm/day when the mean maximum environmental temperature was 100.7℉ D.B. The requirement was found to increase by 0.063 gm/℉ rise in D.B. temperature for 2 hours' exercise. Submitted on September 12, 1958


Blood ◽  
1964 ◽  
Vol 24 (6) ◽  
pp. 780-803 ◽  
Author(s):  
G. E. CARTWRIGHT ◽  
J. W. ATHENS ◽  
M. M. WINTROBE

Abstract Present knowledge concerning the kinetics of granulopoiesis has been reviewed and quantitative data concerning granulokinetics in normal human subjects are presented. A. When granulocytes are labeled in vitro and returned to the circulation of the donor, the distribution of the cells in the circulation and the rate of disappearance of the cells from the circulation can be measured. 1. The total blood granulocyte pool (TBGP) consists of two compartments which are in equilibrium with each other. These pools have been designated the circulating granulocyte pool (CGP) and the marginal granulocyte pool (MGP). The size of the pools has been measured in 109 normal male subjects. The mean values, expressed as numbers of cells x 107 per Kg. of body weight were as follows: TBGP, 70; CGP, 31; and MGP, 39. The mean ratio of the CGP to the TBGP was 0.44. 2. The labeled granulocytes leave the TBGP in an exponential fashion with a mean half-time disappearance (T½) of 6.7 hours as determined in 56 normal male subjects. No evidence has been obtained for a return of granulocytes to the blood. 3. The mean value for the granulocyte turnover rate (GTR) in 56 normal male subjects was 163 x 107 granulocytes per Kg. of body weight per day. Thus, the TBGP turns over 2.3 times per day and the turnover time for the TBGP is 10.4 hours. B. When granulocytes are labeled in vivo by the intravenous administration of DFP32, the rate of disappearance of granulocytes from the circulation and the time required for myelocytes to divide, mature and appear in the blood can be measured. In addition, the generation time of myelocytes can be approximated. From the time parameters and the GTR, the bone marrow pool sizes and turnover times can be calculated. These determinations and calculations have been made for a group of 21 normal male subjects. 1. The mean half-time disappearance (T½) of in vivo labeled granulocytes from the circulation was 7.2 hours. This value agrees well with the value of 6.7 hours obtained after the in vitro labeling of granulocytes. 2. The mean time required for myelocytes to divide, mature and appear in the blood was 11.4 days. 3. The mean generation time of myelocytes was estimated to be not more than 2.9 days. 4. The total granulocyte pool in the bone marrow (neutrophilic myelocytes, neutrophilic metamyelocytes and PMN neutrophils) was calculated to be 186 x 108 cells per Kg. of body weight with a mean turnover time of 11.4 days. The myelocyte pool was estimated to be 41 x 108 cells per Kg. with a turnover time of 2.5 days; the metamyelocyte pool consisted of about 76 x 108 cells per Kg. with a turnover time of 4.7 days; the average size of the mature marrow PMN neutrophil pool was 69 x 108 cells per Kg. of body weight with a turnover time of 4.2 days. C. A kinetic model for granulopoiesis, based on the studies with the DFP32 label, is presented. In this model, myelocytes are depicted as approaching a self-perpetuating population of cells. Some cells enter this population from populations which are less mature but this latter source of cells is small under conditions of normal steady state kinetics. One of the daughter cells of a myelocyte division remains in the myelocyte population to divide again. The other daughter cell enters the metamyelocyte population. The metamyelocyte and PMN neutrophil population is incapable of division and cells move through this population in sequential fashion in the process of maturation. The cells then enter the blood where they equilibrate rapidly between the two blood compartments. The cells are removed from the total granulocyte pool in a random fashion. There is no appreciable pool of granulocytes in the extramedullary tissues of normal subjects and granulocytes do not return from the tissues to the blood. The entire movement of granulocytes from marrow to tissues is uni-directional.


1975 ◽  
Vol 33 (2) ◽  
pp. 141-148 ◽  
Author(s):  
R. S. Watson ◽  
K. M. Etta

1. Skinfold thicknesses, arm circumferences, heights, weights and serum cholesterol levels were determined in ninety-one university students, 207 soldiers and 102 out-patients, all male subjects. Some of these measurements were used to determine the amount of body fat, Quetelet's index and mid-arm muscle circumference2. Quetelet's indices and body-fat values obtained were similar to previously reported values for lean or moderately built males3. Serum cholesterol levels were generally low, with means ranging from 3·98 mmol/1 for 18- to 29-year-old students to 5·19 mmol/l for 40- to 69-year-old out-patients4. The mean values for triceps skinfold thickness, the amount of body fat and serum cholesterol levels for healthy adults obtained in this study are probably normal for northern Nigerian populations5. There was a significant correlation between the amount of body fat and values for triceps and subscapular skinfold thicknesses, Quetelet's index and body-weight for all adults. The correlation between muscle circumference and the amount of body fat was significant for all subjects except adult soldiers.


1971 ◽  
Vol 13 (3) ◽  
pp. 561-563 ◽  
Author(s):  
L. E. Mount ◽  
C. W. Holmes ◽  
W. H. Close ◽  
S. R. Morrison ◽  
I. B. Start

SUMMARYThe voluntary intake of water by 24 groups of 3 to 6 Large White pigs (range of mean body weight: 21 to 73 kg) was measured during a total of 48 periods lasting 3 to 12 weeks each in a large calorimeter equipped as a pig pen. The calorimeter temperature was controlled between 7° and 33°C and the pigs were fed at levels ranging from 42 g feed/kg body weight per day to maximal intake. The mean water: feed ratios were between 2·1 and 2·7 at temperatures between 7° and 22°C, and between 2·8 and 5·0 at 30° and 33°C. The range of mean water consumption extended from 0·092 to 0·184 litre/kg body weight per day.


Author(s):  
P. Spencer Davies

The metabolic or respiratory rate, measured as the aerobic oxygen uptake, of the limpets Patella vulgata L. and P. aspera Lamarck was determined over a range of temperatures in January and in July. In order to determine the effects upon metabolism of adaptation to habitat, P. vulgata living at high shore levels were compared with those living at low shore levels.The respiratory rate is proportional to the power –0·3042 of the fresh body weight and the relationship is not affected by temperature or season, and is the same for both species.There is very little difference in the rates of respiration of equal weight individuals of P. aspera and either group of P. vulgata in January. In July the respiratory rate of low-level P. vulgata and of P. aspera is higher than in January whilst that of the high-level P. vulgata is little changed.The Q10 of respiration had a low value between the temperatures of 15–20° C in both species, and this is thought to represent a hitherto unrecognized form of acclimation to maintain metabolic constancy over the mean environmental temperature range. In P. vulgata low values of Q10 were correlated with high environmental temperatures. Lower Q10's were recorded in July than in January and, in addition, limpets which were adapted to the elevated temperature of high shore levels in July had lower Q10's than the limpets from low shore levels. This apparent acclimation of Q10 was not observed in P. aspera.The significance of the differences in metabolic rate and in Q10 are discussed in relation to acclimation and its importance in the ecological distribution of the two species.


1965 ◽  
Vol 43 (3) ◽  
pp. 351-357 ◽  
Author(s):  
N. T. Gridgeman ◽  
O. Heroux

Statistical analysis of data on the oxygen consumption of rats (Sprague–Dawley strain; records covering several years of experimentation in one laboratory) indicated that the relation between oxygen uptake and body weight is not constant. Kleiber's case for a linear relation between oxygen uptake and the [Formula: see text] power of body weight for homeotherms in general under normal environmental conditions is not impugned by the present findings. Under abnormal experimental conditions, particularly as regards environmental temperature, the use of the analysis of covariance is recommended to best allow for the effect of body weight on oxygen uptake.


1983 ◽  
Vol 100 (2) ◽  
pp. 305-314 ◽  
Author(s):  
J. A. McLean ◽  
A. J. Downie ◽  
C. D. R. Jones ◽  
D. P. Stombaugh ◽  
C. A. Glasbey

SUMMARYBody heat storage changes of cattle were measured by means of simultaneous direct and indirect calorimetry and by thermometry in an environment that alternated in temperature between 12 and 25 °C. When the calorimeter temperature was increased deep body temperature (Tc) increased by approximately 0–5 °C, mean surface temperature (Ts) by 3 °C and mean body temperature (determined from calorimetry, Tb) by 1 °C, but these increases were not fully sustained during the next 24 h. Changes in the three temperatures were related by the equation: δTb = αδTc+(1-α) δTs where a was found to be 0·89±0·027 (S.E.).


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