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The objectives of this study were to investigate the effects of the cow-related factors on rectal temperature (RT) and respiration rate (RR) of lactating dairy cows under different heat stress (HS) conditions and establish the temperature-humidity index (THI) thresholds at which RT and RR begin to increase for cows in China. Cow-related factors included body posture (standing and lying), milk yield (<26 kg/d, ≥ 26-39 kg/d, and ≥39 kg/d), days in milk (≤60 d, > 60 and ≤ 150 d, and >150 d), and parity (1, 2, and ≥3). Records of RT, RR, and individual characteristics were collected from July to October 2020 on a commercial dairy farm in Northern China, where 826 Holstein lactating cows were measured. Using the broken-stick regression models and the entire dataset, the THI thresholds for RT and RR were 69.8 and 67.1, respectively. Therefore, the heat stress conditions during this study were classified according to the THI levels as thermoneutrality (TN, 60 < THI ≤ 67), mild (67 < THI ≤ 72), moderate (72 < THI ≤ 80), and severe (80 < THI ≤ 86). Results showed that lying cows exhibited the higher RT and RR but the lower THI threshold for RT (68.8 vs. 70.7) and RR (65.6 vs. 68.4) than standing cows; milk yield is positively associated with the values of RT and RR under TN or HS conditions, and the THI thresholds for RT (70.2 vs. 70.0 vs. 68.0) and RR (68.1 vs. 64.7 vs. 64.7) were progressively lower for low-yielding, middle-yielding, and high-yielding cows; there was a significant increase in RT and RR in early-lactation cows compared to late-lactation cows under TN or HS conditions (P < 0.001), and the lowest THI threshold (67.8 for RT and 64.7 for RR) was observed in early-lactation cows, followed by mid-lactation cows (68.2 for RT and 65.3 for RR) and late-lactation cows (70.0 for RT and 67.3 for RR); the effects of parity were not significant on RT (P > 0.05), but significant on RR (P < 0.001). The THI thresholds for RT (69.2) and RR (66.0) were lowest for cows in 3rd-parity and higher, followed by cows in 2nd-parity (70.0 for RT and 68.9 for RR) and 1st-parity (70.7 for RT and 66.6 for RR). This study highlighted the great significance of considering the cow-related factors in heat stress responses and THI threshold assessment. For dairy cows in China, we suggest that cooling should be initiated when THI reaches 65 to 66., (Copyright © 2021. Published by Elsevier Ltd.)

This study investigates whether rectal temperature of pigs, prior to slaughter, can give an indication of the risk of developing pork with PSE characteristics. A total of 1203 pigs were examined, measuring the rectal temperature just before stunning, of which 794 rectal temperatures were measured immediately after stunning. pH30LT (M. Longissimus thoracis) and temperature of the ham (Temp30Ham) were collected from about 530 carcasses, 30 min after sticking. The results present a significant positive linear correlation between rectal temperature just before and after slaughter, and Temp30Ham. Moreover, pH30LT is negatively correlated with rectal temperature and Temp30Ham. Finally, a linear mixed model for pH30LT was established with the rectal temperature of the pigs just before stunning and the lairage time. This model defines that measuring rectal temperature of pigs just before slaughter allows discovery of pork with PSE traits, taking into account pre-slaughter conditions., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Regulation of internal body temperature (T b ), or thermoregulation, is an evolutionarily conserved trait that places demand on basal metabolic rate of endothermic animals. Across species, athletes generate increased quantities of heat in comparison to their nonathletic counterparts and, therefore, must mediate physiological unbalance by upregulating the effectiveness of their heat dissipation abilities. Canine athletes are no exception to this phenomenon, however, with literature denoting body temperatures lower than nonathletic canines, it is clear they must possess adaptations to mitigate this demand. With VO 2 max measurements of more than 200 mL/kg/min in sled dogs with mild training to 300 mL/kg/min in highly trained animals, sled dogs are a prime example of athleticism in canines. Seeking to determine correlations between T ear and body mass, morphology, and age of canine athletes, core body temperature (T b ) was measured with an instant ear thermometer, using T ear as a correlate before and after a 2-mile run. In addition, we employed thermal imaging analysis to capture body-wide heat dissipation patterns in sled dogs, and focused on thermal variation of mouth (T mouth ), nose (T nose ), and eyes (T eye ). Furthermore, we looked at correlations between thermal variability across these four tissues and head morphology of each dog. T ear was consistently the highest temperature across all tissues measured, with a 1.5°C increase between pre- to postexercise (p < 0.001). Thermal imaging revealed significant positive correlations between T mouth and body mass 15 min postexercise (p = 0.0023) as well as significantly negative correlations between T nose and body mass at before exercise (p = 0.0468), T eye and nose length after run (p = 0.0076), and T mouth and nose length after run (p = 0.0110). As body temperature rises during exercise, it becomes increasingly important to regulate blood flow throughout the body to supply working tissues with oxygen. This demand is offset by the role of the snout in evaporative cooling through panting, functioning as a prime location for heat dissipation and therefore maintaining significant relationships with many other vascularized tissues., (© 2024 Wiley Periodicals LLC.)

Muscle force production and power output in active males, regardless of the site of measurement (hand, leg, or back), are higher in the evening than the morning. This diurnal variation is attributed to motivational, peripheral, and central factors and higher core and, possibly, muscle temperatures in the evening. This study investigated whether decreasing evening resting rectal temperatures to morning values, by immersion in a water tank, leads to muscle force production and power output becoming equal to morning values in motivated subjects. Ten healthy active males (mean ± SD: age, 22.5 ± 1.3 yrs; body mass, 80.1 ± 7.8 kg; height, 1.72 ± 0.05 m) completed the study, which was approved by the local ethics committee of the university. The subjects were familiarized with the techniques and protocol and then completed three sessions (separated by at least 48 h): control morning (07:30 h) and evening (17:30 h) sessions (with an active 5-min warm-up on a cycle ergometer at 150 W) and then a further session at 17:30 h but preceded by an immersion in cold water (~16.5 °C) to lower rectal temperature (Trec) to morning values. During each trial, three measures of grip strength, isokinetic leg strength measurements (of knee flexion and extension at 1.05 and 4.19 rad s(-1) through a 90° range of motion), and three measures of maximal voluntary contraction (MVC) on an isometric dynamometer (utilizing the twitch-interpolation technique) were performed. Trec, rating of perceived exertion (RPE), and thermal comfort (TC) were also measured after the subjects had reclined for 30 min at the start of the protocol and prior to the measures for grip, isokinetic, and isometric dynamometry. Muscle temperature was taken after the warm-up or water immersion and immediately before the isokinetic and MVC measurements. Data were analyzed using general linear models with repeated measures. Trec values were higher at rest in the evening (by 0.37 °C; p < 0.05) than the morning, but values were no different from morning values immediately after the passive pre-cooling. However, Trec progressively decreased throughout the experiments, this being reflected in the subjects' ratings of thermal comfort. Muscle temperatures also displayed significant diurnal variation, with higher values in the evening (by 0.39 °C; p < 0.05). Right grip strength, isometric peak power, isokinetic knee flexion and extension for peak torque and peak power at 1.05 rad s(-1), and knee extension for peak torque at 4.19 rad s(-1) all showed higher values in the evening (a range of 3-14%), and all other measures of strength or power showed a statistical trend to be higher in the evening (0.10 > p > 0.05). Pre-cooling in the evening significantly reduced force or power variables towards morning values. In summary, effects of time of day were seen in some measures of muscle performance, in agreement with past research. However, in this population of motivated subjects, there was evidence that decreasing evening Trec to morning values by coldwater immersion decreased muscle strength to values similar to those found in the morning. It is concluded that diurnal changes in muscle performance are linked to diurnal changes in Trec.

Twelve Murrah buffaloes in second or third parity during early lactation (50-70 days) were selected from the Institute's herd. All the buffaloes were kept under loose housing system and were provided ad lib green maize fodder and water to drink during 30 days experiment during the month of August-September. The buffaloes were divided into two groups of six each. Showering group (SG) buffaloes were kept under water showers from 11:00 A.M. to 4:00 P.M., while wallowing group (WG) buffaloes were allowed to wallow in a water pond during the same time. Physiological responses viz. rectal temperature (RT), respiration rate (RR), pulse rate (PR) and skin temperature (ST) were recorded before (8.00 A.M.) and after (4.00 P.M.) showers or wallowing. Skin temperature at different sites i.e. trunk, forehead, udder, udder vein, and neck regions was measured. Skin and rectal temperature of both the groups were non significant in morning but varied (P < 0.01) in the evening. Skin temperature measured at all the sites was significantly lower (P < 0.01) in wallowing buffaloes than the showering group. Further, skin temperature of neck, head, udder, udder vein and RT varied (P < 0.01) in SG and WG buffaloes during periods of study. The significant changes in all the parameters of study further support the evidence on effective cooling of skin by wallowing in comparison to water showers. The correlation data indicated a positive correlation of maximum air temperature with RT in SG but correlation was non-significant in WG. RT was positively correlated with ST in SG (P < 0.05) and WG (P < 0.01). The pooled data analysis of both groups also indicated a positive correlation of maximum temperature with RT (P < 0.05). The morning respiration and pulse rate non-significantly varied in both group, however, in the evening, the respiration rate and pulse rate was more (P < 0.01) in SG in comparison to WG. No adverse effect of wallowing or shower treatment on mastitis incidence and general health of animals was observed.

Some synthetic taurine analogues, namely ethanolamine-O-sulphate (EOS), N,N-dimethyltaurine (DMT), N,N,N-trimethyltaurine (TMT) and 2-aminoethylphosphonic acid (AEP) were shown to interact with rabbit brain GABA(A)- or GABA(B)-receptors, while (+/-)piperidine-3-sulfonic acid (PSA) inhibited the activity of rabbit brain 4-aminobutyrate transaminase. This suggests that they behave like direct/indirect GABA agonists or GABA antagonists and affect thermoregulation and gross motor behaviour (GMB) which are under GABA control. In the present study micromole (1.2-48) amounts of these compounds were i.c.v. injected in conscious, restrained rabbits while monitoring rectal temperature (RT), ear skin temperature (EST) and GMB. AEP, EOS, DMT and TMT induced a dose-related hyperthermia, ear vasoconstriction and excitation of GMB, while PSA induced a dose-related hypothermia, ear vasodilation and inhibition of GMB. EOS antagonized in a dose-related fashion hypothermia induced by 60 nmol THIP, a GABA(A) agonist, while AEP, DMT and TMT counteracted that induced by 8 nmol R(-)Baclofen, a GABA(B) agonist. In conclusion, EOS and AEP, DMT, TMT seem to act as GABA(A) and GABA(B) antagonists, respectively, while PSA behaves like an indirect GABA agonist, all affecting the central mechanisms which drive rabbit thermoregulation.

Background: Some studies have suggested that the insertion allele of the ACE gene is associated with endurance performance, including the Ironman triathlon. It is possible that this association is due to genetic linkage between the ACE I/D locus and the T/A variant in intron 4 of the neighbouring GH1 gene. The A variant is associated with lower levels of growth hormone production. Growth hormone has multiple effects, especially on metabolism during exercise and recovery from exercise. Its production during exercise has also been shown to stimulate sweat rate and heat loss., Objective: To determine whether the GH1 gene is associated with the performance and/or post-race rectal temperatures of competitors in the South African Ironman triathlon., Methods: A total of 169 of the fastest finishing white male triathletes who completed the 2000 and/or 2001 South African Ironman triathlon and 155 control subjects were genotyped for the T/A variant in the GH1 gene. Post-race rectal temperature was also determined in 103 of these triathletes., Results: There was no significant difference in the frequency of this polymorphism in the GH1 gene when the fastest finishing triathletes were compared with the control subjects. Post-race rectal temperatures were, however, significantly higher in those triathletes with an AA genotype (mean (SD) 37.7 (0.8) degrees C) compared with those with a TT genotype (37.2 (0.8) degrees C) (p = 0.019)., Conclusions: The T/A polymorphism in intron 4 of the GH1 gene was not associated with performance of the fastest finishers of the South African Ironman triathlon. Post-race rectal temperatures were, however, significantly higher in the fastest finishing athletes, who were homozygous for a GH1 genotype associated with lower growth hormone production.

The effect of heat stress on changes in milk production, rectal temperature, respiratory rate and blood chemistry was evaluated in three groups of six mature Holstein, Jersey and Australian Milking Zebu (AMZ) dairy cows. These animals were subjected to a cool environment when the mean temperature-humidity index (THI) was 72+/-1.4 (dry bulb temperature of 22.2-24.4 degrees C and relative humidity of 100-60%) during the month of December. This experiment was repeated during the hotter month of July of the following year, when the mean THI was 93+/-3.1 (dry bulb temperature of 35.6-43.9 degrees C and relative humidity 95-35%). Holstein cows produced more (p <0.01) milk than AMZ and Jersey cows during the cooler months of the year and all the cows were dry during the hotter months from June until September. Heat stress increased (p<0.01) rectal temperature and respiratory rate in all three breeds. Heat stress had no effect on blood pH in Holstein and AMZ cows but lowered (p <0.01) blood pH from 7.42 to 7.34 in Jersey cows. In addition, heat stress lowered (p <0.01) blood pCO2 (kPa), bicarbonate (HCO3, mmol/L), base excess (BE, mmol/L) and plasma chloride (Cl-, mmol/L) in all three breeds. The total haemoglobin (THb, g/dl) was elevated (p <0.01) in all three breeds when they were subjected to heat stress. Heat stress increased (p<0.01) oxygen saturation (O2SAT, %) in Jersey and AMZ cows but lowered it (p <0.01) in Holstein cows. On the other hand, heat stress increased (p <0.01)pO2 (kPa) in Holstein and Jersey cows but lowered it (p <0.01) in AMZ cows. Heat stress increased (p <0.01) plasma potassium (K, mmol/L) and calcium (Ca, mmol/L) only in Holstein and Jersey cows but lowered them (p<0.01) in AMZ cows. The plasma glucose (GLU, mmol/L) increased (p<0.01) with heat stress in Holstein and AMZ cows but decreased (p <0.01) in Jersey cows. Heat stress increased (p<0.01) plasma creatinine (CR, (mol/L) but lowered (p<0.01) plasma creatinine phosphokinase (CPK, IU/L), aspartate aminotransferase (AST, IU/L) and blood urea nitrogen (BUN, mmol/L) in all three breeds. These results indicate that heat-stressed Holstein and AMZ cows were able to maintain their acid-base balance with a marginal change in their pH of 0.02 when their rectal temperatures increased by 0.47 and 0.38 degrees C, respectively. When heat stress increased the rectal temperature in Jersey cows by 0.70 degrees C, the pH decreased (p<0.01) from 7.42 to 7.34. However, even with this decrease 0.08 the pH is still within the lower physiological limit of 7.31.

Objective: To determine whether a full-body spandex garment would alter rectal temperatures of healthy dogs at rest in cool and warm environments., Design: Prospective study., Animals: 10 healthy dogs., Procedures: Each dog was evaluated at a low (20 degrees to 25 degrees C [68 degrees to 77 degrees F]) or high (30 degrees to 35 degrees C [86 degrees to 95 degrees F]) ambient temperature while wearing or not wearing a commercially available whole-body spandex garment designed for dogs. Oxygen consumption was measured by placing dogs in a flow-through indirect calorimeter for 90 to 120 minutes. Rectal temperature was measured before dogs were placed in the calorimeter and after they were removed., Results: Rectal temperature increased significantly more at the higher ambient temperature than at the lower temperature and when dogs were not wearing the garment than when they were wearing it. The specific rate of oxygen consumption was significantly higher at the lower ambient temperature than at the higher temperature., Conclusions and Clinical Relevance: Results suggest that wearing a snug spandex body garment does not increase the possibility that dogs will overheat while in moderate ambient temperatures. Instead, wearing such a garment may enable dogs to better maintain body temperature during moderate heat loading. These results suggest that such garments might be used for purposes such as wound or suture protection without causing dogs to overheat.

1. In order to ascertain whether both GABA(A) and GABA(B), or only GABA(B) receptors, directly modulate thermoregulation in conscious rabbits, GABA(A)/GABA(B) agonist and antagonist agents were injected intracerebroventricularly in conscious rabbits while monitoring changes in rectal temperature (RT), gross motor behaviour (GMB) and electrocorticogram (ECoG) power spectra (ps) from sensorimotor cortices. 2. GABA (48 micromol), nipecotic acid (50 nmol), THIP (60 nmol), muscimol (18 nmol) and baclofen (8 nmol) induced hypothermia (-deltaRTmax values of 1.70+/-0.1, 1.4+/-0.2, 1.0+/-0.4, 1.1+/-0.2 and 1.6+/-0.3 degrees C, respectively), accompanied by inhibition of GMB and ECoG synchronization. THIP increased ps at delta frequency band (1.1-3.3 Hz), while GABA, nipecotic acid, muscimol and baclofen did the same at both delta and (4.6-6.5 Hz) frequency bands. ECoG ps changes were concomitant or even preceded hypothermia. 3. Bicuculline (1.8 nmol) induced hyperthermia (deltaRTmax 1.2+/-0.5 degrees C) and slight excitation of GMB, while CGP35348 (1.2 micromol) did not affect RT nor GMB. Both compounds did not affect ECoG ps. 4. Bicuculline potentiated muscimol-induced hypothermia, inhibition of GMB and synchronization of ECoG, while CGP35348 fully antagonized these effects. 5. In conclusion, the present results, while confirming the prevailing role of GABA(B), also outline a direct involvement of GABA(A) receptors in the central mechanisms of thermoregulation. Ascending inhibition towards discrete cortical areas controlling muscular activity and thermogenesis may result from GABA receptor activation in neurones proximal to the ventricles, thus contributing to hypothermia, although hypothermia-induced reduction of neuronal activity of these cortical areas cannot be ruled out.

The aim of this study was to evaluate the effect of scrotal cooling on rectal temperature in man. Pilot studies suggested that immersing the scrotum in a 30 degrees C water bath increased rectal temperature, but immersing the scrotum in a 0 degree C water bath did not. Six healthy young men immersed their scrotums in a 35 degrees C water bath for 11 min followed by 21 min at 30 degrees C. Rectal temperature rose by 0.38 +/- 0.04 degrees C (P < 0.01) in response to the 30 degrees C water bath. Repetition of the study by immersing the hands instead of the scrotum in the water bath had no effect on rectal temperature. The scrotum appears to play a role in human temperature regulation.

Selective brain cooling (SBC) is defined as a brain temperature cooler than the temperature of arterial blood from the trunk. Surrogate measures of arterial blood temperature have been used in many published studies on SBC. The use of a surrogate for arterial blood temperature has the potential to confound proper identification of SBC. We have measured brain, carotid blood, and rectal temperatures in conscious sheep exposed to 40, 22, and 5 degrees C. Rectal temperature was consistently higher than arterial blood temperature. Brain temperature was consistently cooler than rectal temperature during all exposures. Brain temperature only fell below carotid blood temperature during the final few hours of 40 degrees C exposure and not at all during the 5 degrees C exposure. Consequently, using rectal temperature as a surrogate for arterial blood temperature does not provide a reliable indication of the status of the SBC effector. We also show that rapid suppression of SBC can result if the animals are disturbed.

This review is the final contribution to a four-part, historical series on human exercise physiology in thermally stressful conditions. The series opened with reminders of the principles governing heat exchange and an overview of our contemporary understanding of thermoregulation (Part 1). We then reviewed the development of physiological measurements (Part 2) used to reveal the autonomic processes at work during heat and cold stresses. Next, we re-examined thermal-stress tolerance and intolerance, and critiqued the indices of thermal stress and strain (Part 3). Herein, we describe the evolutionary steps that endowed humans with a unique potential to tolerate endurance activity in the heat, and we examine how those attributes can be enhanced during thermal adaptation. The first of our ancestors to qualify as an athlete was Homo erectus, who were hairless, sweating specialists with eccrine sweat glands covering almost their entire body surface. Homo sapiens were skilful behavioural thermoregulators, which preserved their resource-wasteful, autonomic thermoeffectors (shivering and sweating) for more stressful encounters. Following emigration, they regularly experienced heat and cold stress, to which they acclimatised and developed less powerful (habituated) effector responses when those stresses were re-encountered. We critique hypotheses that linked thermoregulatory differences to ancestry. By exploring short-term heat and cold acclimation, we reveal sweat hypersecretion and powerful shivering to be protective, transitional stages en route to more complete thermal adaptation (habituation). To conclude this historical series, we examine some of the concepts and hypotheses of thermoregulation during exercise that did not withstand the tests of time., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

In this, the second of four historical reviews on human thermoregulation during exercise, we examine the research techniques developed by our forebears. We emphasise calorimetry and thermometry, and measurements of vasomotor and sudomotor function. Since its first human use (1899), direct calorimetry has provided the foundation for modern respirometric methods for quantifying metabolic rate, and remains the most precise index of whole-body heat exchange and storage. Its alternative, biophysical modelling, relies upon many, often dubious assumptions. Thermometry, used for >300 y to assess deep-body temperatures, provides only an instantaneous snapshot of the thermal status of tissues in contact with any thermometer. Seemingly unbeknownst to some, thermal time delays at some surrogate sites preclude valid measurements during non-steady state conditions. To assess cutaneous blood flow, immersion plethysmography was introduced (1875), followed by strain-gauge plethysmography (1949) and then laser-Doppler velocimetry (1964). Those techniques allow only local flow measurements, which may not reflect whole-body blood flows. Sudomotor function has been estimated from body-mass losses since the 1600s, but using mass losses to assess evaporation rates requires precise measures of non-evaporated sweat, which are rarely obtained. Hygrometric methods provide data for local sweat rates, but not local evaporation rates, and most local sweat rates cannot be extrapolated to reflect whole-body sweating. The objective of these methodological overviews and critiques is to provide a deeper understanding of how modern measurement techniques were developed, their underlying assumptions, and the strengths and weaknesses of the measurements used for humans exercising and working in thermally challenging conditions., (© 2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)

It was found that the rectal temperature of rabbits restricted by a normal neck stock position dropped about 1.2-1.5 degrees C when the restriction position changed from a normal restriction to a supine restriction position. This temperature change was also reversible. We studied the mechanisms of this phenomenon from a thermodynamic point of view and obtained the following results: 1) The rectal temperature of rabbit restricted in the supine position did not increase after the injection of lipopolysaccharide (LPS). 2) In the supine restricted rabbit, endogenous pyrogen which was induced by the injection of LPS to these rabbits appeared the same as the control. 3) Some pharmaceuticals (urethan, iproniazid, atropin and hexamethonium) did not show any influence on the drop of rectal temperature in either normal or supine restrictions. 4) The rectal temperature of shorn rabbits dropped more than that of normal rabbits in both normal and supine restrictions. 5) When the normal restriction position was changed to the supine and prone restriction positions, the mean surface temperature was also decreased. From these results, it was concluded that rabbit rectal temperature was changed with a change in the restriction position which could change the surface skin area.

A group of 22 young subjects staying in rest was studied in the aim to follow the nycthemeral evolution of the rectal temperature, according to two situations: 1) normal feeding, 2) absence of feeding. The use of drinking water was not limited. The experimentation was carried out in tropical area, Kédougou (Eastern Senegal), during a high period of temperature. The mean of day temperature was 38 degrees C and the night temperature, 22 degrees C. The skin and rectal temperature, the arterial pressure and the cardiac frequency were measured every three hours. The results showed a significant difference in the nycthemeral rythm of the rectal temperatures. The nocturnal temperatures were not different in the two conditions. We observed a significant elevation (delta = 0.31 +/- 0.18 degree C) of the diurne post prandial temperature. The results supported that the thermic modification observed during the experience were linked to the feed.

Mean rectal temperatures in neonates were investigated during sleep state transitions as assessed by visually analyzed electroencephalographic-polygraphic recordings. Continuous 3-hour studies were obtained on 3 term and 5 preterm infants at postconceptional term ages using a 24-channel computerized monitoring system. In the study, 1,461 min were assigned an EEG state by traditional criteria. Mean rectal temperature measurements were tabulated for each minute of sleep. Data were analyzed both as 1,461 consecutive minutes of sleep, and as 28 complete ultradian neonatal sleep cycles. Exploratory analyses were performed using t tests, Mann-Whitney U tests, and one-way analysis of variance. Decreases in mean rectal temperatures followed a transition from active to quiet sleep for only the term group. The preterm group had higher temperatures at sleep onset than the term group and demonstrated no changes during state transitions. Higher temperatures were maintained in the preterm group during both active and quiet sleep (i.e., 36.7 degrees C versus 36.4 degrees C, P = .02) when 28 complete cycles of sleep were compared and during the transition when 658 min of active sleep were compared to 617 min of quiet sleep. These findings are preliminary; however, the phenomenon of state-dependent changes in mean rectal temperature in neonates based on electroencephalographic sleep is unreported. Higher mean rectal temperatures during active sleep and altered temperature responses during transition to quiet sleep in the preterm infant suggest altered brain function because of the preterm infant's adaptation to the extrauterine experience.

Metabolic and temperature data were collected for 56 patients with burns managed with four wound care protocols. Group I (n = 7) treated with dressings and variable ambient temperature selected for patient subjective comfort; group II (n = 7) managed without dressings and variable ambient temperature for patient comfort; group III (n = 6) no dressings, ambient temperature of 25 degrees C and the output of electromagnetic heaters adjusted for patient comfort; group IV (n = 36) dressings and ambient temperature of 28 degrees C. All groups were cold challenged: groups I and II by sequentially lowering ambient temperature, group III by decreasing the electromagnetic heater output, and group IV by removing dressings with ambient temperature remaining at 28 degrees C. Only groups II and IV demonstrated correlation between percent body surface area burn and heat production. The slope of the regression for group IV neutral was significantly less than that for group IV cold and group II neutral and cold. The relationship between percent body surface area burn and rectal temperature for groups I, II, and III neutral was equal to .03 degrees C increase in rectal temperature per 1% body surface area burn (Y = 37 + 0.03; r = 0.74; df 18; p < 0.01) and was not significantly different when cold. This predicts a 1.5 degrees C increase in rectal temperature for a patient with a 50% body surface area burn who does not have sepsis.(ABSTRACT TRUNCATED AT 250 WORDS)

This study was conducted to examine the guinea pig as a suitable model for the study of the postburn hypermetabolic response and the febrile response that accompanies burn injury in man. Thirty animals were randomly assigned to four groups: > 50% body surface area burn (n = 6); 45% to 50% body surface area burn (n = 10); < 45% body surface area burn (n = 6); and controls (n = 8). On postburn days 3, 7, 11, 13, and 15, sequential temperature measurements were made. On postburn days 7 to 15, the randomly selected burn group (n = 12) and the control group (n = 8) had calorimetry studies performed. Sequential rectal temperature data demonstrate that the guinea pig does not mount a prolonged or consistent febrile response after burn injury (p > 0.05 for burn group vs control group on postburn days 7 to 13; p < 0.05 for postburn days 3 and 15 only). However, the burned guinea pig is significantly hypermetabolic after burn injury, with significant increases in dry and evaporative heat loss. The hypermetabolic response was proportional to burn wound size. Guinea pigs are not an ideal model for the study of the postburn febrile response; however, this is an excellent model for the study of postburn hypermetabolism.

Despite many attempts to relate components of physique to core temperature cooling rate, no consistent relationship has emerged. The inconsistencies among the reported findings may arise from unaccounted thermoregulatory responses or incomplete physique assessment or both. A study was designed to examine this relationship in the range of rectal temperatures (Tre) within which shivering and sweating are absent, defined as the null zone, thus minimizing the contribution of these effector responses. Twenty healthy subjects (10 male and 10 female), representing a variety of physiques, participated in the study. The anthropometric protocol included 5 heights, body mass, 8 skinfolds, 10 girths, and 4 breadths. This permitted derivation of a body surface-area-to-mass ratio and estimates of adipose and muscle tissue masses using a cadaver-validated mass fractionation model. Subjects were heated in a 40 degrees C bath followed immediately by cooling in a 30.6 degrees C bath. During the cooling, forehead sweating rate and oxygen uptake were monitored to establish the boundaries of the Tre null zone. In addition, on-line recordings were made of Tre, skin temperature, and surface heat flux at six sites. The rate of cooling of Tre (Tre), in the range of temperatures between thresholds for sweating and shivering, was correlated to the components of physique. Estimates of adipose and skeletal muscle tissue masses did not correlate to Tre in the range of core temperatures investigated. However, total mass exhibited a significant correlation (r = 0.5, P less than or equal to 0.05) with Tre, but gender seemed to distort this relationship, possibly due to differences in adipose tissue distribution.

98 test coolings were made under various cooling conditions (moving air, two types of both clothing and covering) on dummies of real masses of 1, 3.3, 9.9, 24.5 and 33.4 kg resp. which cool under standard conditions (unclothed, uncovered, still air) like human bodies of 14, 33, 41, 83 and 104 kg resp. The results provide evidence on a nonlinear dependence of corrective factors of body weight upon the body weight. The dynamics of the dependence increases with the thickness of thermic isolation. Transferred to the use of the nomogram method on bodies, cooling conditions requiring corrective factors known by experience between 0.75 (moving air) and 1.3 (rather thin clothing/covering) can be used as in the past independent on the body weight. Only in higher corrective factors for thicker clothing/covering according to experience the dependence of corrective factors on the body weight must be taken into account in bodies of a very high or low body weight. Beside a simplified table a formula for computing is also given for that purpose.

During 3 baseline nights (2 for adaptation) and during 3 days of a sleep-wake reversal, electrophysiological characteristics of sleep and rectal temperature were recorded in 8 morning-type (M-type) and 8 evening-type (E-type) subjects, living in a quiet sleep laboratory. Outcomes of visual sleep scoring revealed the following general tendencies for day-sleep as compared to night-sleep: shorter sleep latencies, shorter REM (rapid eye movement sleep) latencies, advance of the time of maximum REM duration, increased duration of slow wave sleep, more intermittent wakefulness, and decreased subjective sleep quality. Furthermore, for the M-types consistently shorter sleep latencies and--for day-sleep--longer REM latencies were observed than those for the E-types. With regard to the parabolic time course of REM duration, M-types appeared to be relatively phase advanced, in particular for their day-sleep. In addition, subjective sleep quality was consistently higher for the M-types, with the exception of the first day-sleep. The temporal distributions of EEG delta (0.5-3.5 Hz) energy over the first four NREM/REM cycles of day-sleep all deviated from a monotonically decreasing trend. Compared to night-sleep the M-types showed a relative increase of delta energy for Cycle 2, whereas for the E-types a relative increase for Cycles 3 and 4 was observed. An analysis of delta energy, employing a pattern-recognition technique independently from visual sleep scoring, revealed an overall faster rate of accumulation for the M-types. Following sleep onset, rectal temperature showed a decrement, which was larger for the M-types. Moreover, rectal temperature and delta energy were negatively related, as indicated by a negative mean intra-individual correlation. These results are discussed in relation to the characteristic sleep-wake behavior of M-types and E-types.

This study was designed to determine the factors predicting the post-race rectal temperature in marathon runners. Post-race rectal temperatures of 30 recreational runners (maximum oxygen consumption (VO2max) = 58.3 +/- 5.9 ml O2.kg-1.min-1; mean +/- SD) who completed a 42.2 km marathon at 75.8% (+/- 9.3%) VO2max were measured and related to their levels of dehydration (percent mass loss), their running velocities (km.h-1), and their estimated absolute metabolic rates (1 O2.min-1) for different segments of the 42.2 km race. The influence of certain anthropometric variables was also determined. Percent mass loss during the race (2.5 +/- 1.4%), post-race rectal temperatures (38.9 +/- 0.6 degrees C), and rates of sweat loss (1.0 +/- 0.3 1.h-1) were low. There was no statistical relationship between percent mass loss and post-race rectal temperature. Post-race rectal temperatures were significantly related to the metabolic rates for the full 42.2 km and for the last 21.1 and 6 km of the race, and to the average running velocity for the last 6 km (P less than 0.05 and P less than 0.01). Average sweat rates were related to metabolic rates for 42.2 km and for the last 6 km of the race (P less than 0.05) but were unrelated to running velocity. We conclude that metabolic rate sustained during the latter section of the race, and not the level of dehydration, is the principal determinant of the post-race rectal temperature in marathon runners.

The application of the rectal temperature time of death nomogram at the scene of death by 11 authors from 6 lego-medical institutes resulted in a standard deviation of the differences between nomographic and real death time of +/- 1.3 h in 46 cases (group I) with met requirements and clearly defined points of contact, nevertheless, including 9 cases with a more progressive cooling (0.5 greater than Q greater than or equal to 0.2). In cases with a real death time of more than 4h (N = 26) the standard deviation was +/- 1.0 hours corresponding to permissible variation of 95% of +/- 2.0 hours. Consequently, the permissible variation of 95% was much smaller than that suggested by the nomogram. The nomographic death time interval did not agree with the real one in 5 cases out of additional 30 cases with recognizably unsure points of contact (group II).

Cattle control body temperature in a narrow range over varying climatic conditions. Endogenous body heat is generated by metabolism, digestion and activity. Radiation is the primary external source of heat transfer into the body of cattle. Cattle homeothermy uses behavioural and physiological controls to manage radiation, convection, conduction, and evaporative exchange of heat between the body and the environment, noting that evaporative mechanisms almost exclusively transfer body heat to the environment. Cattle control radiation by shade seeking (hot) and shelter (cold) and by huddling or standing further apart, noting there are intrinsic breed and age differences in radiative transfer potential. The temperature gradient between the skin and the external environment and wind speed (convection) determines heat transfer by these means. Cattle control these mechanisms by managing blood flow to the periphery (physiology), by shelter-seeking and standing/lying activity in the short term (behaviourally) and by modifying their coats and adjusting their metabolic rates in the longer term (acclimatisation). Evaporative heat loss in cattle is primarily from sweating, with some respiratory contribution, and is the primary mechanism for dissipating excess heat when environmental temperatures exceed skin temperature (~36°C). Cattle tend to be better adapted to cooler rather than hotter external conditions, with Bos indicus breeds more adapted to hotter conditions than Bos taurus. Management can minimise the risk of thermal stress by ensuring appropriate breeds of suitably acclimatised cattle, at appropriate stocking densities, fed appropriate diets (and water), and with access to suitable shelter and ventilation are better suited to their expected farm environment., (© 2023 The Authors. Australian Veterinary Journal published by John Wiley & Sons Australia, Ltd on behalf of Australian Veterinary Association.)

Clinical Scenario: Exertional heat stroke (EHS) is a medical emergency characterized by body core temperatures >40.5°C and central nervous system dysfunction. An EHS diagnosis should be immediately followed by cold-water immersion (CWI). Ideally, EHS victims cool at a rate >0.15°C/min until their temperature reaches 38.9°C. While generally accepted, these EHS treatment recommendations often stem from research that examined only males. Since gender differences exist in anthropomorphics (eg, body surface area, lean body mass) and anthropomorphics impact CWI cooling rates, it is possible that CWI cooling rates may differ between genders. Clinical Question: Do CWI rectal temperature (Trec) cooling rates differ between hyperthermic males and females? Summary of Findings: The average Trec cooling rate across all examined studies for males and females was 0.18 (0.05) and 0.24 (0.03)°C/min, respectively. Hyperthermic females cooled ∼33% faster than males. Clinical Bottom Line: Hyperthermic females cooled faster than males, most likely because of higher body surface area to mass ratios and less lean body mass. Regardless of gender, CWI is highly effective at lowering Trec. Clinicians must be able to treat all EHS victims, regardless of gender, with CWI, given its high survival rate when implemented appropriately. Strength of Recommendation: Moderate evidence (2 level 3 studies) suggests that females cool faster than males when treated with CWI following severe hyperthermia. Despite gender differences, cooling rates exceeded cooling rate recommendations for EHS victims (ie, 0.15°C/min). [ABSTRACT FROM AUTHOR]

Domestic dogs demonstrate a positive correlation between body mass and whole-animal metabolism but a negative relationship between body mass and lifespan in dogs. Additionally, essential physiological mechanisms in domestic dogs, such as the relationships between thermal relations and body size and age, remain poorly understood. In this study, we looked at thermoregulation in dogs of different sizes, ages, coat types, and head morphologies across three different seasons. We used tympanic membrane temperatures (T ear ) and infrared thermography to observe temperature regulation in pet dogs before and after a 45-min moderate walking exercise trial. We hypothesized that Tear and heat dissipation is positively correlated with body mass. Using network analysis, we found that body mass was among the most central features for spring and summer trials, but not for the winter trials. Similarly, leg length, snout length, and paw width were the central predictors in two of the three seasons. Mediation analysis demonstrated that nose and snout length act as significant mediators of the effects of body mass on mouth temperatures in the spring. For the summer trials, nose length and paw width significantly mediated the effect of body mass on mouth temperatures. Age, however, does not seem to be a major determinant of thermoregulation in dogs according to best subset models. A cross-seasonal examination of repeated measurements showed that mouth temperature heat dissipation rates decreased with increasing temperature and humidity. Overall, our findings support our hypothesis that T ear and heat dissipation rates are positively correlated with body mass in dogs, thus, negatively correlated with mass-specific metabolism. This finding suggests that small dogs allocate a bigger proportion of their metabolism to "inefficiencies" of heat production to offset greater heat loss., (© 2022. The Author(s), under exclusive licence to Springer Nature B.V.)

Cold-water immersion (CWI) is the best treatment for patients with exertional heat stroke (EHS), and rectal temperature (Trec) cooling rates may differ between sexes. Previous authors have suggested that the body surface area (BSA):lean body mass (LBM) ratio is the largest factor affecting CWI Trec cooling rates in men with hyperthermia; this has never been confirmed in women with hyperthermia. To examine whether the BSA:LBM ratio and other anthropometric characteristics affect Trec cooling rates in women with hyperthermia. Cross-sectional study. Laboratory. Sixteen women were placed in either a low BSA:LBM ratio (LOW; n = 8; age = 22 ± 1 years, height = 166.8 ± 6.0 cm, mass = 64.1 ± 4.5 kg, BSA:LBM ratio = 3.759 ± 0.214 m2/kg·102) or high BSA:LBM ratio (HIGH; n = 8; age = 22 ± 2 years, height = 162.7 ± 8.9 cm, mass = 65.8 ± 12.7 kg, BSA:LBM ratio = 4.161 ± 0.232 m2/kg·102) group. On day 1, we measured physical characteristics using dual-energy x-ray absorptiometry, and participants completed a maximal oxygen consumption test. On day 2, participants walked at 4.8 km/h for 3 minutes and then ran at 80% of their predetermined maximal oxygen consumption for 2 minutes in the heat (temperature = ∼40°C, relative humidity = 40%). This sequence was repeated until Trec reached 39.5°C. Then they underwent CWI (temperature = ∼10°C) until Trec was 38°C. Rectal temperature and CWI cooling rates. The groups had different BSA:LBM ratios (P =.001), LBM (LOW: 45.8 ± 3.0 kg; HIGH: 41.0 ± 5.1 kg; P =.02), and body fat percentages (LOW: 25.7% ± 5.0%; HIGH: 33.7% ± 6.3%; P =.007) but not different BSA (LOW: 1.72 ± 0.08 m2; HIGH: 1.70 ± 0.16 m2; P =.40) or body mass index (LOW: 23.1 ± 2.1; HIGH: 24.9 ± 4.7; P =.17). Despite differences in several physical characteristics, Trec cooling rates were excellent but comparable (LOW: 0.26°C/min ± 0.09°C/min; HIGH: 0.27°C/min ± 0.07°C/min; P =.39). The BSA:LBM ratio (r = 0.14, P =.59), BSA (r = −0.01, P =.97), body mass index (r = 0.37, P =.16), and body fat percentage (r = 0.29, P =.28), LBM (r = −0.10, P =.70) were not correlated with Trec cooling rates. Body anthropometric characteristics did not affect CWI Trec cooling rates in women with hyperthermia. Therefore, clinicians need not worry that anthropometric characteristics might slow CWI treatment in women with severe hyperthermia. [ABSTRACT FROM AUTHOR]

Evolution of rectal temperature (Tre) during recovery in different air temperatures was studied following different patterns of heat load before and after adaptation to work in heat (10 consecutive days). Three subjects have been exposed, after a 30 min rest period (Ta=28degrees C, Pwa=14 mb) to 4 heat loads, each producing 1 degreeC increase in Tre in approximatively 30 min (Co:Ta= 50 degrees C, Pwa = 60 mb, W = O watt; C1; 50 degrees C, 42 mb, 50 W on bicycle ergometer; C2;39 degrees C, 38 mb, 100 W and C3: 28 degrees C, 31 mb, 150 W). After of these heat loads, subjects were allowed to recover during 2 h at Ta = 28, 22 or 16 degrees C (Pwa = 14 mb). Results show that: (a) the cooler was the Ta, the faster was the recovery time; (b) before adaptation occurs, the evolution of Tre depended on the preceding heat load pattern; (c) the more intense was the work load, the more the adaptation reduced time for subsequent recovery. The interaction obtained between adaptation and intensity of preceding work load is discussed. The evolutions of leg skin temperatures suggest that a decreased local heat conductance (of inferior limbs) is associated with a local increase in external heat exchange. Adaptation to work in heat would take the form of a local re-adjustment of internal and external heat exchanges.

Information on body temperature is frequently lacking in metabolic studies on normal and malnourished suckling rats although differences in their thermoregulatory efficiency may be expected. The aim of the present study was to evaluate the effect of different ambient temperatures on the rectal temperature of litters of normal and protein deprived rats to establish the ambient temperatures at which a normal rectal temperature can be expected at various postnatal ages. The offspring of normal rats and rats subjected to a dietary reduction of 50% of the protein intake were examined 10 days to 30 days postnatally. The pups were transferred from the nest cage to an incubator: the rectal temperature was measured immediately after transfer to the incubator and 30 and 60 min later at ambient temperatures of 35, 30 and 25 degrees C. Up to 15 days of age control pups showed a fall in rectal temperature after the short exposure to room temperature (22 degrees C) needed for transfer. A similar fall of rectal temperature was recorded in the malnourished pups up to 25 days age. The effects of the ambient temperatures on the malnourished pups indicated a delay in the control of body temperature of some 10 days. This is in agreement with a previous report on semi-starved rats (Heim & Szelenyi 1965). The conditions for the maintenance of a normal rectal temperature in litters of normal and malnourished suckling rats separated from their mother are out-lined.

To determine if rectal temperature is an adequate index of brain temperature during changing thermal conditions, we measured rectal, cerebral cortical, and carotid arterial blood temperatures simultaneously during whole body cooling in adult cats. The mean steady state rectal, brain and carotid arterial temperatures at the onset of cooling were: 39.2 +/- 0.2, 38.5 +/- 0.2, and 38.3 +/- 0.3 degrees C, respectively. Rectal temperature decreased faster than both brain and arterial blood, while only a small temperature difference was observed between brain and arterial blood, brain always exceeding blood. Rectal temperature cannot be considered an adequate index of brain temperature. Carotid arterial temperature is a better estimate of brain temperature.

1. Subcutaneous injections of capsaicin (mean cumulative dose: 80.1 +/- 3.6 mg , kg-1) permanently reduced the capacity of rats to withstand a hot environment when deprived of water. With water available, hyperthermia was discrete or absent in capsaicinized rats in hot environment. 2. Desensitization was followed by a significant decrease in both food intake and body weight. Treated rats recovered normal body weight after 3 weeks. 3. In a hot environment, compared to controls, food intake was significantly increased in capsaicin desensitized rats which maintained their body weight. In cold environment, food intake was decreased in capsaicin desensitized rats which lost body weight. At normal ambient temperature, food intake and body weight were similar in the 2 groups. 4. Caloric intake adjustment at high and at low temperatures was therefore disturbed in capsaicin desensitized rats. It is concluded that hypothalamic thermodetectors implicated in both thermoregulation and food intake behaviour could be partially damaged by capsaicin.

19 small premature infants in servocontrol incubators, whose abdominal skin temperature was 36.0 +/- 0.3 degrees C, were subjected to alternate high- and low-humidity environments. With low humidity, rectal temperature dropped significantly below abdominal skin temperature. Skin was the predominant site of evaporative heat loss. The temperature was lower on naked skin than on an area covered by adhesive tape. Thus, servocontrol with low humidity increases evaporative heat loss and engenders a cycle of events that results in paradoxical body temperature decrease as the incubator temperature increases.