PubMed Health⌕ Search

SEARCH · PubMed Health

Results for “Body Temperature”

Explore indexed PubMed citations for clinical trials, systematic reviews and public health research. Read source abstracts and follow each citation to its original PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 145 records · Page 8Linked to original sources

Daily and estrous rhythmicity of body temperature in domestic cattle.

BACKGROUND: Rhythmicity in core body temperature has been extensively studied in humans and laboratory animals but much less in farm animals. Extending the study of rhythmicity of body temperature to farm animals is important not only from a comparative perspective but also from an economic perspective, as greater knowledge of this process can lead to improvements in livestock production practices. In this study in cattle, we investigated the maturation of the daily rhythm of body temperature in newborn calves, characterized the parameters of the daily rhythm in young cows, and studied the oscillation in body temperature associated with the estrous cycle in adult cows. RESULTS: We found that the daily rhythm of body temperature is absent at birth but matures fully during the first two months of life. The mature rhythm had a mean level of 38.3 degrees C, a range of excursion of 1.4 degrees C, and was more robust than that of any mammalian species previously studied (90% of maximal robustness). Sexually mature cows also exhibited a robust estrous rhythm of body temperature. An elevation of about 1.3 degrees C was observed every 21 days on the day of estrus. Small seasonal variations in this pattern were observed. CONCLUSION: In conclusion, calves exhibit a very robust daily rhythm of body temperature, although this rhythm is absent at birth and develops during the first two months of life. Adult cows exhibit also 21-day rhythmicity in body temperature reflecting the duration of the estrous cycle.

Age Factors↗

The use of voided urine temperature in the determination of basal body temperature.

The temperature of freshly voided urine has been shown to be a reliable predictor of body temperature. This relationship was confirmed for the measurement of BBT. A method was described for patients to obtain their BBT in a way that they may find more convenient than obtaining either oral or rectal temperature. The BBT graph patterns generated from the temperature of freshly voided urine closely paralleled those generated by oral temperature.

Body Temperature↗

Light masking of circadian rhythms of heat production, heat loss, and body temperature in squirrel monkeys.

Whole body heat production (HP) and heat loss (HL) were examined to determine their relative contributions to light masking of the circadian rhythm in body temperature (Tb). Squirrel monkey metabolism (n = 6) was monitored by both indirect and direct calorimetry, with telemetered measurement of body temperature and activity. Feeding was also measured. Responses to an entraining light-dark (LD) cycle (LD 12:12) and a masking LD cycle (LD 2:2) were compared. HP and HL contributed to both the daily rhythm and the masking changes in Tb. All variables showed phase-dependent masking responses. Masking transients at L or D transitions were generally greater during subjective day; however, L masking resulted in sustained elevation of Tb, HP, and HL during subjective night. Parallel, apparently compensatory, changes of HL and HP suggest action by both the circadian timing system and light masking on Tb set point. Furthermore, transient HL increases during subjective night suggest that gain change may supplement set point regulation of Tb.

Animals↗

Axillary and thoracic skin temperatures poorly comparable to core body temperature circadian rhythm: results from 2 adult populations.

Data from 2 separate studies were used to examine the relationships of axillary or thoracic skin temperature to rectal temperature and to determine the phase relationships of the circadian rhythms of these temperatures. In study 1, axillary skin and rectal temperatures were recorded in 19 healthy women, 21 to 36 years of age. In study 2, thoracic skin and rectal temperatures were recorded in 74 healthy women, 39 to 59 years of age. In both studies, temperatures were recorded continuously for 24 h while subjects carried out normal activities. Axillary and thoracic probes were insulated purposely to prevent ambient effects. Cosinor analysis was employed to estimate circadian rhythm mesor, amplitude, and acrophase. In addition, correlations between temperatures at various measurement sites were calculated and agreement determined. The circadian timing of axillary and skin temperature did not closely approximate that of rectal temperature: the mean acrophase (clock time) for study 1 was 18:57 h for axillary temperature and 16:12 h for rectal; for study 2, it was 03:05 h for thoracic and 15:05 h for rectal. Across individual subjects, the correlations of axillary or thoracic temperatures with rectal temperatures were variable. Results do not support the use of either axillary or skin temperature as a substitute for rectal temperature in circadian rhythm research related to adult women.

Adult↗

[Influences of the complex of environmental temperature, relative humidity and air velocity on the body temperature of restrained mice (author's transl)].

Effects of the complexes of environmental factors, such as ambient-temperature, relative humidity and air velocity, on the body temperature were investigated in restrained mice. Observations were carried out before and after 60 min-exposure to various triple combinations among environmental temperatures of 15, 25 and 35 degreesC, relative humidities of 40, 65 and 90%, and air velocities of 0.2, 1.0 and 2.0 m/sec. The analysis of variance about the differences of body temperature revealed significant effects of the environmental temperature and the air velocity levels, while no significant effects were recognized of the relative humidity. Effects of the double factors, either the environmental temperature plus the relative humidity or the environmental temperature plus the air velocity, were significant at 5 or 1% level respectively. However, effects of the double factors the relative humidity plus the air velosity, as well as the triple factors were not significant. Under the environments consisted of triple factors, the environmental temperature of 20 and 25 degreesC, the relative humidities of 40 and 70% and the air velocities of 0.1 and 0.5 m/sec, significant effects at 1% level were recognized only in the environmental temperature levels. In the relative humidty or the air velocity levels, and the double or triple factor levels, no significant effects were recognized. From the results obtained, the effective temperature (Te) was indicated by the formula, Te=t+100x-v square root 38-t, in which were given the environmental temperature in t degrees C, the absolute humidity in x kg/kg and the air velocity in v m/sec.

Air Movements↗

Lack of integrative control of body temperature after capsaicin administration.

BACKGROUND: Body temperature is usually regulated by opposing controls of heat production and heat loss. However, systemic administration of capsaicin, the pungent ingredient of hot peppers, facilitated heat production and heat loss simultaneously in rats. We recently found that the capsaicin-induced heat loss and heat production occur simultaneously and that the biphasic change in body temperature is a sum of transient heat loss and long-lasting heat production. Moreover, suppression of the heat loss response did not affect capsaicin-induced heat production and suppression of heat production did not affect capsaicin-induced heat loss. These observations suggest the independent peripheral mechanisms of capsaicin-induced thermal responses. Thus, the capsaicin-induced thermal responses apparently lack an integrated control. METHODS: Male Wistar rats were maintained at an ambient temperature of 24 +/- 1 degrees C on a 12 h on-off lighting schedule at least for two weeks before the experiments. They were anesthetized with urethane (1.5 g/kg, i.p.) and placed on a heating pad, which was kept between 29 and 30 degrees C. Skin temperature(Ts) was measured with a small thermistor, which was taped to the dorsal surface of the rat's tail, to assess vasoactive changes indirectly. Colonic temperature(Tc) was measured with another thermistor inserted about 60 mm into the anus. O2 consumption was measured by the open-circuit method, and values were corrected for metabolic body size (kg0.75). Capsaicin (Sigma) was dissolved in a solution comprising 80% saline, 10% Tween 80, and 10% ethanol, and injected subcutaneously at a dose of 5 mg/kg. Each rat received a single injection of capsaicin because repeated administration of capsaicin renders an animal insensitive to the subsequent administration of capsaicin. Laminectomy was performed at the level of the first and second cervical vertebrae to expose the cervical spinal cord for sectioning. The brain was transected at 4-mm rostral from the interaural line with an L-shaped knife. RESULTS: After administration of capsaicin, O2 consumption increased from 13.5 +/- 0.4 mL/min/kg0.75 at 0 min to a peak of 15.9 +/- 0.4 mL/min/kg0.75 at 71 min and gradually declined but remained higher than the basal value until the end of the 4-h observation period. Ts also immediately increased from 27.7 +/- 0.2 degrees C to 31.9 +/- 0.3 degrees C at 39 min, and it returned to the baseline level within 90 min after the capsaicin administration. Tc initially decreased from 37.1 +/- 0.1 degrees C to 36.8 +/- 0.2 degrees C at 43 min and then gradually increased over the baseline level and remained at 37.6 +/- 0.2 degrees C until the end of the experiment. In spinalized rats, the capsaicin-induced increases in O2 consumption was largely attenuated, while the basal O2 consumption was similar to that of control rats. The basal Ts of spinalized rats was 32.4 +/- 0.3 degrees C, which was higher than that of control rats. Capsaicin increased Ts by less than 1 degree C, and Tc did not change after the capsaicin administration. O2 consumption of decerebrated rats was statistically higher than that of control rats after the injection of capsaicin. However, capsaicin did not increase Ts, showing a lack of a vasodilatory response. Decerebration between the hypothalamus and midbrain prevented the capsaicin-induced heat loss but not the heat production response. CONCLUSION: These results show that the capsaicin-induced heat production and heat loss are controlled separately by the brainstem and by the forebrain, respectively, and suggest that the body temperature regulation is performed without an integrative center.

Animals↗

Seasonal patterns in body temperature of free-living rock hyrax (Procavia capensis).

Rock hyrax (Procavia capensis) are faced with large daily fluctuations in ambient temperature during summer and winter. In this study, peritoneal body temperature of free-living rock hyrax was investigated. During winter, when low ambient temperatures and food supply prevail, rock hyrax maintained a lower core body temperature relative to summer. In winter body temperatures during the day were more variable than at night. This daytime variability is likely a result of body temperatures being raised from basking in the sun. Body temperatures recorded during winter never fell to low levels recorded in previous laboratory studies. During summer ambient temperatures exceeded the thermoneutral zone of the rock hyrax throughout most of the day, while crevice temperatures remained within the thermoneutral zone of rock hyrax. However, in summer variation in core body temperature was small. Minimum and maximum body temperatures did not coincide with minimum and maximum ambient temperatures. Constant body temperatures were also recorded when ambient temperatures reached lethal limits. During summer it is likely that rock hyrax select cooler refugia to escape lethal temperatures and to prevent excessive water loss. Body temperature of rock hyrax recorded in this study reflects the adaptability of this animal to the wide range of ambient temperatures experienced in its natural environment.

Acclimatization↗

[Limitation of heat loss in long-lasting paediatric operations by means of a metal foil--positive correlation between room and body temperature (author's transl)].

A controlled clinical prospective study in 80 children showed the efficiency of an aluminium-coated polyester foil as a protection against heat loss during long-lasting (greater than or equal to 2 h) orthopaedic correcting operations. A pronounced correlation between theatre temperature and the body temperature of the children wrapped in foil could be demonstrated. This method is recommended as a safe and low-cost routine preventive measure for a major part of anaesthetics in paediatric surgery. The foil effect could be completed further by infusion solutions warmed to body temperature and an operation theatre temperature raised to 22-24 degrees C.

Age Factors↗

Body temperature control in sepsis-induced acute lung injury.

Body temperature is precisely regulated to maintain homeostasis in homeothermic animals. Although it remains unproved whether change of body temperature constitutes a beneficial or a detrimental component of the septic response, temperature control should be an important entity in septic experiments. We investigated the effect of body temperature control on the lipopolysaccharide (LPS)-induced lung injury. Acute lung injury in rats was induced by intratracheal spray of LPS and body temperature was either clamped at 37 degrees C for 5 hours or not controlled. The severity of lung injury was evaluated at the end of the experiment. Intratracheal administration of aerosolized LPS caused a persistent decline in body temperature and a significant lung injury as indicated by an elevation of protein-concentration and LDH activity in the bronchoalveolar lavage (BAL) fluid and wet/dry weight (W/D) ratio of lungs. Administration of LPS also caused neutrophil sequestration and lipid peroxidation in the lung tissue as indicated by increase in myeloperoxidase (MPO) activity and malondialdehyde (MDA) production, respectively. Control of body temperature at 37 degrees C after LPS (LPS/BT37, n = 11) significantly reduced acute lung injury as evidenced by decreases in BAL fluid protein concentration (983 +/- 189 vs. 1403 +/- 155 mg/L) and LDH activity (56 +/- 10 vs. 123 +/- 17 deltamAbs/min) compared with the LPS group (n = 11). Although the W/D ratio of lung and MDA level were lower in the rats received temperature control compared with those received LPS only, the differences were not statistically significant. Our results demonstrated that intratracheal administration of aerosolized LPS induced a hypothermic response and acute lung injury in rats and controlling body temperature at a normal range may alleviate the LPS-induced lung injury.

Animals↗

Seasonal and daily rhythms of body temperature in the European hamster (Cricetus cricetus) under semi-natural conditions.

Body temperature of five European hamsters exposed to semi-natural environmental conditions at 47 degrees N in Southern Germany was recorded over a 1.5-year period using intraperitoneal temperature-sensitive radio transmitters. The animals showed pronounced seasonal changes in body weight and reproductive status. Euthermic body temperature changed significantly throughout the year reaching its maximum of 37.9 +/- 0.2 degrees C in April and its minimum of 36.1 +/- 0.4 degrees C in December. Between November and March the hamsters showed regular bouts of hibernation and a few bouts of shallow torpor. During hibernation body temperature correlated with ambient temperature. Monthly means of body temperature during hibernation were highest in November (7.9 +/- 0.8 degrees C) and March (8.2 +/- 0.5 degrees C) and lowest in January (4.4 +/- 0.7 degrees C). Using periodogram analysis methods, a clear diurnal rhythm of euthermic body temperature could be detected between March and August, whereas no such rhythm could be found during fall and winter. During hibernation bouts, no circadian rhythmicity was evident for body temperature apart from body temperature following ambient temperature with a time lag of 3-5 h. On average, hibernation bouts lasted 104.2 +/- 23.8 h with body temperature falling to 6.0 +/- 1.7 degrees C. When entering hibernation the animals cooled at a rate of -0.8 +/- 0.2 degrees C.h-1; when arousing from hibernation they warmed at a rate of 9.9 +/- 2.4 degrees C.h-1. Warming rates were significantly lower in November and December than in January and February, and correlated with ambient temperature (r = -0.46, P < 0.01) and hibernating body temperature (r = -0.47, P < 0.01). Entry into hibernation occurred mostly in the middle of the night (mean time of day 0148 hours +/- 3.4 h), while spontaneous arousals were widely scattered across day and night. For all animals regression analysis revealed free-running circadian rhythms for the timing of arousal. These results suggest that entry into hibernation is either induced by environmental effects or by a circadian clock with a period of 24 h, whereas arousal from hibernation is controlled by an endogenous rhythm with a period different from 24 h.

Animals↗

Physicians' perceptions regarding body temperature in health and disease.

Although body temperature has been monitored for more than a century as a means of distinguishing health from disease, physicians' perceptions of concepts of clinical thermometry are largely unknown. To characterize such perceptions, we did a descriptive analysis of responses to a survey questionnaire dealing with body temperature. Seventy-five percent of the 268 physicians and physicians-in-training surveyed offered 37 degrees C (98.6 degrees F) as their definition of "normal body temperature." Only 10 (4%) specified a particular body site (eg, oral or rectal) of temperature measurements in their definition. Although 98% believed that body temperature normally varies during the day, there was not a consensus as to the magnitude of such variability. There was also considerable disagreement as to the specific temperatures defining the lower and upper limits of the febrile range. Subjects exhibited a clear preference for the Fahrenheit scale in their responses. Medical students differed significantly from graduate physicians in several of the areas examined.

Body Temperature↗

Body temperature regulation in rats during exercise of various intensities at different ambient temperatures.

We examined the relationship between body temperature, tail vasomotor response, and work intensity at different ambient temperatures in rats, using a treadmill and continuously measuring oxygen uptake during exercise. At an ambient temperature (Ta) of 24 degrees C, rectal temperature (Tre) at the beginning of tail vasodilation during exercise increased in proportion to work intensity. After tail vasodilation Tre remained steady, and at the end of 30 min exercise Tre level was proportional to work intensity. At Ta of 14 degrees C, Tre at the end of exercise was slightly higher than at 24 degrees C, and was higher at higher work intensities. At Ta of 4 degrees C, Tre rose slower during exercise than at higher Tas and even dropped at relatively low work intensities. Tail vasodilation did not occur in most cases. At Ta of 34 degrees C, Tre rose continuously during exercise. These data indicate that body temperature of rats during exercise rises in proportion to work intensity, but the extent of body temperature rises differs according to Ta.

Animals↗

[Influence of body temperature on outcome of head injuries].

OBJECTIVE: To investigate the influence of body temperature on the outcome of head injuries. METHODS: The data of body temperature and outcomes of patients with head injuries admitted to Tiantan Hospital between July 1997 and July 1999 was analyzed retrospectively. The admission temperature was divided into 4 groups: hypo-temperature (with body temperature < 36 degrees C), normal temperature (36.0 degrees C approximately 37.2 degrees C), mild hyper-temperature (37.3 degrees C approximately 38.3 degrees C) and significant hyper-temperature (> 38.3 degrees C). Appraisal was made at discharge and one year later using GOS criteria (grade 1 approximately 2 were regarded as unfavorable prognosis, and grades 3 approximately 5 as favorable prognosis). Chi-square test and logistic regression analysis were performed using SPSS statistic software. RESULTS: The outcome of the patients with significant high admission temperature and hypo-temperature was unfavorable. The difference between different temperature groups, except the hypo-temperature group and significant high temperature group, was significant (P < 0.01). The higher admission temperature means less favorable outcome. The outcome of the hypo-temperature and hyper-temperature groups was less favorable than that of the normal temperature group (P < 0.01). The difference in the 15 factors such as temperature, age, etc, between the group with favorable prognosis and the group with unfavorable prognosis (P < 0.01). However, the difference in hemoglobin and hematocrit between the group with favorable prognosis and the group with unfavorable prognosis was unsignificant. The value of B at discharge and 1 year after injury were -0.809 and -1.104 respectively. CONCLUSION: The admission body temperature can be used as an independent predictor for prognosis of head injuries. The low- and the high temperature predict the worse outcome. The higher the body temperature is, the less favorable the outcome. Admission body temperature has a significant influence on the outcome of head injuries.

Adolescent↗

Variation in the sensitivity of organismal body temperature to climate change over local and geographic scales.

Global climate change is expected to have broad ecological consequences for species and communities. Attempts to forecast these consequences usually assume that changes in air or water temperature will translate into equivalent changes in a species' organismal body temperature. This simple change is unlikely because an organism's body temperature is determined by a complex series of interactions between the organism and its environment. Using a biophysical model, validated with 5 years of field observations, we examined the relationship between environmental temperature change and body temperature of the intertidal mussel Mytilus californianus over 1,600 km of its geographic distribution. We found that at all locations examined simulated changes in air or water temperature always produced less than equivalent changes in the daily maximum mussel body temperature. Moreover, the magnitude of body temperature change was highly variable, both within and among locations. A simulated 1 degrees C increase in air or water temperature raised the maximum monthly average of daily body temperature maxima by 0.07-0.92 degrees C, depending on the geographic location, vertical position, and temperature variable. We combined these sensitivities with predicted climate change for 2100 and calculated increases in monthly average maximum body temperature of 0.97-4.12 degrees C, depending on location and climate change scenario. Thus geographic variation in body temperature sensitivity can modulate species' experiences of climate change and must be considered when predicting the biological consequences of climate change.

Animals↗

Intracellular pH in lizard Dipsosaurus dorsalis in relation to changing body temperatures.

Mean whole-body and tissue-specific intracellular pH values (pHi) were measured in Dipsosaurus dorsalis by the dimethyloxazolidinedione technique. pHi was measured in lizards at constant body temperatures (Tb) (18, 25, 35, and 42 degrees C) and in lizards undergoing changes in Tb between 18 and 42 degrees C. Constant Tb between 18 and 42 degrees C maintained for 24 h or more produced a delta pH/delta Tb of -0.015 for the mean whole-body, -0.012 for venous blood, -0.0104 for cardiac muscle, and -0.0098 for skeletal muscle. Within the preferred range of Tb values (35-42 degrees C), the delta pH/delta Tb patterns were closer to that expected to achieve constant dissociation of protein imidazole (approximately -0.017): mean whole-body -0.020, cardiac muscle -0.016, and skeletal muscle -0.018. Tissue water contents were independent of Tb. Whole-body pHi during gradual warming and cooling (approximately 2 h elapsed time for each direction) closely corresponded to steady-state values. Upon cooling to 18 degrees C, tissue-specific and whole-body pHi often fell 0.1-0.2 unit below that expected; in each case this was correlated with an extracellular acidosis. A gradual recovery of pHi occurred with the recovery of the extracellular acidosis. Over the normally experienced Tb range, adjustments in pHi apparently rapidly achieve steady-state values and are in accord with the imidazole alphastat hypothesis. These patterns are discussed in terms of the thermal ecology of Dipsosaurus.

Animals↗

Core body temperature and sleep of older female insomniacs before and after passive body heating.

The purpose of this study was to investigate the relationship between core body temperature and sleep in older female insomniacs and changes in that relationship as a result of passive body heating (PBH). An increase in body temperature early in the evening by way of PBH in older female insomniacs increased SWS in the early part of the sleep period and improved sleep continuity. Fourteen older female insomniacs (60-73 years old) participated in at least two consecutive nights of PBH involving hot (40-40.5 degrees C) baths 1.5-2 hours before bedtime. Hot baths resulted in a significant delay in the phase of the core body temperature rhythm compared to baseline nights. This delay in temperature phase paralleled the improvements in sleep quality.

Adult↗

[The relationship between fecal kinetics and body temperature in elderly people].

The relationship between fecal kinetics and body temperature was examined in elderly people. The subjects consisted of 34 hospitalized patients over 65 years of age (11 males aged 66-82 years, with a mean age of 70.3 years; and 23 females aged 65-84 years, with a mean age of 72.1 years). Then mean age of all subjects was 71.5 years. The subjects were divided into two groups: the non-constipation (NCP) group (patients who had been evacuating at least once daily) and the constipation (CP) group (patients who had not evacuated for 3 days or more). In the CP group, we analyzed the lowest and highest body temperature during two consecutive days (the day of evacuation and the previous day) and the lowest body temperature during another two days (the day of evacuation and the following day). In the NCP group, 3 consecutive days were selected at random for analyzing the lowest body temperature on the first day, the highest body temperature on the second day and the lowest body temperature on the third day. In the CP group, the body temperature before evacuation was 37.3 degrees C or more in 6 of the 28 patients (21.4%). In the NCP group, the highest body temperature before evacuation averaged 36.39 degrees C and the lowest body temperature after evacuation averaged 36.0 degrees C, with a temperature difference of 0.39 degrees C between the pre- and post-evacuation periods.(ABSTRACT TRUNCATED AT 250 WORDS)

Aged↗