scholarly journals Cold-induced heat production preceding shivering

2005 ◽  
Vol 93 (3) ◽  
pp. 387-391 ◽  
Author(s):  
Anne M. J. van Ooijen ◽  
Wouter D. van Marken Lichtenbelt ◽  
Anton A. van Steenhoven ◽  
Klaas R. Westerterp

Individual changes in heat production and body temperature were studied in response to cold exposure, prior to shivering. The subjects ten women (seven men) were of normal weight, had a mean age of 23 (SD 3) years and average BMI 22·2 (SD 1·6) Kg/m2. They were lying supine under thermoneutral conditions for 30 min and were subsequently exposed to air of 15°C until shivering occurred. Heat production was measured with a ventilated hood. Body composition was measured with underwater weighing and 2H dilution. Body temperatures were measured with thermistors. Heat production during cold exposure prior to shivering increased and reached a plateau. Skin temperature decreased and did not reach a plateau during the test period. The non-shivering interval (NSI) ranged from 20 to 148 min, was not related to body composition and was not significantly different between women (81 (sd 15) min) and men (84 (sd 34) min). NSI was negatively related to skin temperature (r2 0·44, P=0·004), and skin temperature was related to heat production (r2 0·39, P=0·007) In conclusion, subjects with a relatively large heat production during cold exposure maintained a relatively high skin temperature but showed a short NSI, independent of differences in body composition.

1959 ◽  
Vol 14 (1) ◽  
pp. 43-45 ◽  
Author(s):  
M. B. Kreider ◽  
P. F. Iampietro ◽  
E. R. Buskirk ◽  
David E. Bass

Effects of continuous cold stress on 24-hour patterns of body temperature were studied in five men. Cold stress consisted in living at 15.6℃ (60℉) for 14 days wearing only shorts. The cold period was preceded and followed by 2 weeks at 26.7℃ (80℉). Activity (minimal) and diet were the same for all periods. One blanket was used at night. Rectal temperature (Tr) and skin temperature (Ts) were measured. Tr during sleep fell more rapidly and to lower values during cold exposure (35.6℃) than during the control period (36.1℃). Ts during sleep was slightly lower in the cold than in the control period; also, Ts did not exhibit the gradual drop characteristic of sleep in the control period. Comparison of Tr and Ts between early and later cold days revealed the following differences: a) nocturnal Tr fell to lower levels on the later cold days; b) nocturnal toe temperatures were 15℃ (27℉) higher on the later cold days. The arch temperatures followed the same pattern as the toes. No significant differences were found in daytime temperatures between early and later cold days. The data suggest that evidence for acclimatization to cold in terms of altered body temperature responses may be fruitfully sought in responses during rewarming and/or sleep. Submitted on September 19, 1958


1964 ◽  
Vol 19 (1) ◽  
pp. 9-12 ◽  
Author(s):  
Jacques Leblanc ◽  
M. Pouliot ◽  
S. Rheaume

Previous studies have shown a decreased response in fishermen to cold applied locally. In the present study, the same subjects, when exposed naked for 1 hr at 60 F maintained a higher skin temperature than a control group. If these findings indicate a decreased vasoconstriction, all results obtained to date on these fishermen would indicate a decreased adrenergic response. Evidence of gross shivering was much more pronounced in the fishermen but this was not reflected by greater heat production. Both groups excreted more hydroxycortisone in the cold, and the excretion was higher in the control subjects. Cold exposure did not increase the catecholamine excretion in either group. Note: (With the Technical Assistance of P. Tousignant) acclimatization; body temperature; skin temperature; vasomotor adaptation; shivering; adrenergic response in cold habituation; hydroxycortisone excretion in cold stress Submitted on June 17, 1963


1991 ◽  
Vol 69 (7) ◽  
pp. 1842-1847 ◽  
Author(s):  
Gregory K. Snyder ◽  
Joseph R. Coelho ◽  
Dalan R. Jensen

In chicks the ability to regulate body temperature to adult levels develops during the first 2 weeks of life. We examined whether the ability of young chicks to regulate body temperature is increased by elevated levels of the thyroid hormone 3,3′5-triiodothyronine. By 13 days following hatch, body temperatures of chicks were not significantly different from those expected for adult birds. Furthermore, at an ambient temperature of 10 °C, 13-day-old control chicks were able to maintain body temperature, and elevated serum thyroid hormone levels did not increase rates of oxygen consumption or body temperature above control values. Six-day-old chicks had body temperatures that were significantly lower than those of the 13-day-old chicks and were not able to regulate body temperature when exposed to an ambient temperature of 10 °C. On the other hand, 6-day-old chicks with elevated serum thyroid hormone had significantly higher rates of oxygen consumption than 6-day-old control chicks, and were able to maintain constant body temperatures during cold exposure. The increased oxygen consumption rates and improved ability to regulate body temperature during cold exposure were correlated with increased citrate synthase activity in skeletal muscle. Our results support the argument that thyroid hormones play an important role in the development of thermoregulatory ability in neonate birds by stimulating enzyme activities associated with aerobic metabolism.


Author(s):  
Claudia Irene Maushart ◽  
Jaël Rut Senn ◽  
Rahel Catherina Loeliger ◽  
Judith Siegenthaler ◽  
Fabienne Bur ◽  
...  

Abstract Context Thyroid hormone is crucial for the adaptation to cold. Objective To evaluate the effect of hyperthyroidism on resting energy expenditure (REE), cold-induced thermogenesis (CIT) and changes in body composition and weight. Design Prospective cohort study. Setting Endocrine outpatient clinic at tertiary referral center. Patients Eighteen patients with overt hyperthyroidism. Main Outcome Measures We measured REE during hyperthyroidism, after restoring euthyroid TH levels and after 3 months of normal thyroid function. In fourteen patients energy expenditure (EE) was measured before and after a mild cold exposure of two hours and CIT was the difference between EEcold and EEwarm. Skin temperatures at eight positions were recorded during the study visits. Body composition was assessed by dual X-ray absorption. Results Free T4 (fT4) and free T3 (fT3) decreased significantly over time (fT4, p=0.0003; fT3, p=0.0001). REE corrected for lean body mass (LBM) decreased from 42 ± 6.7 kcal/24h/kg LBM in the hyperthyroid to 33±4.4 kcal/24h/kg LBM (-21%, p<0.0001 vs hyperthyroid) in the euthyroid state and three months later to 33 ± 5.2 kcal/24h/kg LBM (-21%, p=0.0022 vs. hyperthyroid, overall p<0.0001). Free T4 (p=0.0001) and free T3 (p<0.0001) were predictors of REE. CIT did not change from the hyperthyroid to the euthyroid state (p=0.96). Hyperthyroidism led to increased skin temperature at warm ambient conditions but did not alter core body temperature, nor skin temperature after cold exposure. Weight regain and body composition were not influenced by REE and CIT during the hyperthyroid state. Conclusions CIT is not increased in patients with overt hyperthyroidism.


1983 ◽  
Vol 54 (4) ◽  
pp. 1025-1031 ◽  
Author(s):  
S. D. Livingstone ◽  
J. Grayson ◽  
J. Frim ◽  
C. L. Allen ◽  
R. E. Limmer

Rectal, esophageal, auditory canal, gastrointestinal tract, and sublingual temperature were recorded on five young Caucasian males who, in an environment of -32 degrees C and 11-km/h wind, sat during one 90-min exposure and walked on a treadmill at 2.9 km/h during another. The clothing permitted cooling of their torsos while giving adequate protection to their extremities. Control exposures involved subjects sitting in still air at 24–26 degrees C dressed only in thermal underwear. In the control environment all of the internal body temperatures measured gave comparable and consistent values; however, cold exposure affected the various sites differently. Esophageal temperatures fluctuated rapidly as a result of subjects swallowing cold saliva. Sublingual temperatures were below the lower limit of a clinical thermometer, possibly because of facial cooling. Auditory canal temperatures were low, perhaps also because of facial cooling. Rectal temperatures were high as were the gastrointestinal tract temperatures, due perhaps to local heat production in response to cold stimulation. Metabolic rate increased initially in the cold and again toward the end of the cold exposure.


1960 ◽  
Vol 55 (3) ◽  
pp. 295-302 ◽  
Author(s):  
R. B. Symington

Responses in body, skin and coat temperatures, cardio-respiratory frequencies and rate of moisture secretion of ewes of three breeds to the diurnal fluctuation in ambient temperature were recorded in the presence and absence of drinking water during the hottest part of the Rhodesian year.1. At 7.0 a.m. body temperatures were: Merino 102·8° F.; Persian 102·2° F. and Native 101·5° F. Between 7·0 a.m. and 1·0 p.m. body temperature rose almost equally in Persians and Natives and fell slightly in Merinos. Change in body temperature between 7.0 a.m. and 1.0 p.m. was not affected significantly by availability of water nor age of ewe, but varied with type of thermal burden (i.e. solar insolation only v. solar insolation plus artificial heat) when water was not available. Although air temperature fell towards late afternoon body temperature of Merinos and Natives rose appreciably, that of Persians only slightly.2. At 7·0 a.m. respiratory rates were (cyc./min.): Merino 59·6; Persian 43·0; Native 29·9. Increase in rate of respiration was the main thermolytic mechanism in all breeds. Merinos had a lower threshold of respiratory response to rising ambient temperature than either hair breed but increase in rate of respiration between 7.0 a.m. and 1.0 p.m. did not differ significantly with breed or age.3. No breed appeared to use the peripheral blood system in thermoregulation. Cardio-frequency, as a measure of this blood flow, remained almost constant with a slight tendency to fall with rise in ambient temperature.4. In all breeds skin temperature was related to ambient and body temperatures; consequently the diurnal fluctuation in skin temperature differed in wool and hair breeds. When thermal burden was greatest Merino skin temperature fell, that of hair breeds did not.Except at 11.0 a.m. there was a gradient between rectal, skin and air temperatures. Direct elimination of heat was thus possible for 23 hr. each day.5. In hair breeds moisture secretion depended on insensible perspiration; consequently, rate of moisture secretion changed with body and air temperatures. In Merinos moisture for skin surface evaporation was provided by sensible and insensible perspiration. Natives may be able to sweat at temperatures higher than those recorded but it is unlikely Persians have a sweating mechanism.6. In all breeds coat temperature was related closely to ambient temperature and changes in solar conditions evoked immediate response in coat temperature. Merino fleece apparently stabilized skin temperature whereas Persian and Native hair did not.


1976 ◽  
Vol 54 (2) ◽  
pp. 101-106 ◽  
Author(s):  
Q. J. Pittman ◽  
W. L. Veale ◽  
K. E. Cooper

Prostaglandins appear to be mediators, within the hypothalamus, of heat production and conservation during fever. We have investigated a possible role of prostaglandins in the nonfebrile rabbit during thermoregulation in the cold. Shorn rabbits were placed in an environment of 20 °C, and rectal and ear skin temperatures, shivering and respiratory rates were measured. A continuous intravenous infusion of leucocyte pyrogen was given to establish a constant fever of approximately 1 °C, and after observation of a stable febrile temperature for 90 min, a single injection of 300 mg of sodium salicylate, followed by a 1.5 mg/min infusion was then given. After the salicylate infusion was begun, rectal temperature began to fall, and reached nonfebrile levels within 90 min. Shivering activity ceased, respiratory rates increased, and in two animals, ear skin temperature increased. When these same rabbits were placed in an environment of 10 °C, at a time they were not febrile, and an identical amount of salicylate was given, rectal and ear skin temperatures, shivering and respiratory rates did not change. These results indicate that prostaglandins do not appear to be involved in heat production and conservation in the nonfebrile rabbit.


1959 ◽  
Vol 52 (3) ◽  
pp. 305-312 ◽  
Author(s):  
W. Bianca

1. Three calves were exposed in a climatic room to an environment of 40° C. dry-bulb and 38° C. wet-bulb temperature for up to 110 min. each day for 1-2 weeks.2. These exposures produced progressive changes in the physiological reactions of the animals to heat:(a) Rectal temperature and skin temperature (for a given time of exposure) declined. In consequence there was a marked increase in the tolerance time, i.e. in the time for which the animals could withstand the hot environment before reaching a rectal temperature of 42° C.(b) Respiratory rate rose earlier and assumed higher levels (for given levels of body temperature).(c) Heart rate decreased markedly.3. These changes are discussed in relation to heat loss and heat production and have been interpreted as reflecting chiefly a reduction in the metabolic heat production of the animals.


1970 ◽  
Vol 48 (1) ◽  
pp. 1-10 ◽  
Author(s):  
James F. O'Hanlon Jr. ◽  
Steven M. Horvath

Thirty-four men were exposed to 8 °C for 2 h. Their reactions were studied to indicate how physiological relationships change during exposure to cold. Measurements of various body temperatures, MST, MBT, body heat content (BHC), [Formula: see text], heat production, and heart rate (HR) were made before the onset of and periodically during cold exposure. Various skin temperatures fell to different levels while rectal temperature rose slightly, then fell 0.3 °C by the end of the exposure. BHC declined by 6%, [Formula: see text] nearly doubled, [Formula: see text] and heat production increased by 66 and 75% respectively, and HR changed little during cold exposure. Relationships which changed most significantly during cold exposure were those between MST and rectal temperature, certain skin temperatures and rectal temperature, [Formula: see text] (also heat production) and BHC, [Formula: see text] and rectal temperature, and finally, those between every body temperature and the age of the subjects. Relationships which also changed were those between finger and toe temperature as well as those between [Formula: see text] (also heat production) and each of the following: [Formula: see text], rectal temperature, thigh temperature, HR, and age. These results indicated that (1) temperature in the upper extremities was actively maintained at a higher level than temperature in the lower extremities, (2) increased metabolism became a progressively more effective adaptation than redistribution of blood volume, (3) subjects with the lowest BHC tended to increase their metabolism the most, (4) [Formula: see text] was inversely related to core temperature after the latter fell below normal, (5) HR was unrelated to the increase in [Formula: see text], (6) the usual inverse relationship between age and metabolism was not found in the cold, and finally, (7) older subjects generally tended to maintain higher body temperatures than younger subjects.


1960 ◽  
Vol 198 (3) ◽  
pp. 471-475 ◽  
Author(s):  
T. R. A. Davis ◽  
D. R. Johnston ◽  
F. C. Bell ◽  
B. J. Cremer

When cold acclimating rats are treated with diathermy, curare and a combination of both, two main fractions of the increase in cold-induced oxygen consumption can be delineated. First, a fraction which diathermy replaces by virtue of the fact that it, in the intensities used, can raise core temperature without altering the temperature of the skin; therefore this fraction appears to be dependent upon changes in central temperature and is found to persist throughout the period of acclimation investigated. Second, a fraction of cold-induced oxygen consumption which is not replaced by diathermy and which is presumed to be dependent upon changes in skin temperature. By the administration of curare, this second fraction can be separated into two further fractions acting reciprocally depending upon the duration of cold exposure. In the early stages of acclimation, the curare-suppressed fraction of oxygen consumption appears to be entirely due to shivering. As shivering disappears with acclimation, it is replaced by a peripherally regulated nonshivering heat source which eventually takes over all the duties of heat production previously performed by shivering.


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