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Effects of environmental temperature on heat production associated with food intake and on abdominal temperature in laying hens.

An experiment was carried out to verify the relationship between the heat production associated with food intake and environmental temperature. Four laying hens were trained to eat two meals per day and were kept under artificial illumination with dark, dim and light periods. 2. Metabolic heat production was measured using two open-circuit respiratory chambers. Abdominal temperatures were measured, using thermocouples, at environmental temperatures of 12, 16, 20, 24, 28, 32 and 36 degrees C and at food intakes of 90, 60, 30 and 0 g/d. 3. The rate of heat production was dependent on both environmental temperature and food intake. Increasing environmental temperature resulted in a decrease in total metabolic rate at any food intake, indicating that heat production associated with food intake was not directly linked with thermoregulation at low environmental temperatures. 4. Abdominal temperature varied little with either food intake or environmental temperature below 28 degrees C. Above 28 degrees C, abdominal temperature increased with both environmental temperature and quantity of food, indicating that the heat production associated with food intake adds to the heat load at high environmental temperatures. 5. Both heat production and abdominal temperature declined with decreasing light intensity and increased before feeding time. These effects were considered to result from changes in physical activity.

Abdomen↗

Does forehead liquid crystal temperature accurately reflect "core" temperature?

Liquid crystal thermometry (LCT) is a non-invasive alternative to temperature monitoring. We evaluated the ability of forehead LCT, rectal temperature, and axillary skin temperature to trend distal oesophageal temperature during rapid warming on cardiopulmonary bypass. In 24 patients undergoing open heart surgery, temperatures were measured during the rapid warming phase on bypass (12-35 min). Scattergrams of temperature vs time for the four temperature sites each contained 150 data points. Polynomial regression analysis revealed that LCT, but not axillary or rectal temperatures, correlated with oesophageal temperature. We conclude that forehead LCT may be useful to monitor temperature trends and to detect rapid elevations in body temperature when more invasive temperature monitoring is inappropriate or unavailable.

Analysis of Variance↗

The effects of variation in body temperature on the preferred water temperature and flow rate during showering.

The purpose of this study was to investigate the effects of body temperature variations on subjects' preferred water temperature and flow rate during showers. Nine healthy women students took a shower before and after physical exercise (running on a treadmill for 30 min) and water immersion (immersing in the water of 25 degrees C temperature for 30 min). During each shower, the subject was instructed to adjust both the water temperature and flow rate of a shower to suit their comfort. Rectal temperature and skin temperatures of the subjects, water temperature, and flow rate of the shower were measured during the experiments. The means of preferred water temperature during showers were 40.2 degrees C and 43.8 degrees C before and after water immersion respectively, which were significantly different. On the other hand, there was little difference in the preferred water temperature between before and after the treadmill exercise. There were no significant differences in the flow rates between before and after both water immersion and the treadmill exercise. A significant negative relationship was observed between the mean body temperature (Tb) and the preferred water temperature during showers (r = -0.439). On the other hand, no significant relationship was found between Tb and the preferred flow rate. Moreover, a significant negative relationship was observed between the preferred water temperature and the flow rate during showers (r = -0.528).

Adult↗

The effect of environmental temperature on immune response and metabolism of the young chicken. 5. Effect of low environmental temperature on the humoral immune response to sheep red blood cells in relation to energy metabolism.

The effect of low environmental temperature on the humoral immune response to sheep red blood cells (SRBC) was investigated in relation to energy metabolism. Two experiments were done with 3- to 6-week-old pullets using two climate respiration chambers. During both experiments a standard temperature regimen of constant 25 C was maintained in one chamber, whereas the temperature in the other chamber was constant 10 C (Experiment 1) or fluctuated between 5 to 15 C (Experiment 2). The relative humidity was held at 70% at all temperature regimens. Feed allowance was such that growth rates at the two temperatures within experiment were expected to be similar. Indeed, growth rate and body weight were not significantly (P greater than .05) influenced by temperature in Experiment 1. Feed consumption at 10 C was 32.7% above that at 25 C. At 5 to 15 C feed consumption was 34.1% higher than at 25 C, whereas growth rate was reduced (P less than .05) by 8%. At 0 and 10 days after injection, differences in hemagglutinin anti-SRBC antibody titers (log2) between temperatures within each experiment were not significant. The 2-mercaptoethanol resistant (2-MEr) antibody titers 5 days after injection were increased by 26% (P less than .05) at 10 C compared to 25 C. The fluctuating low temperature reduced 2-MER antibody titers 5 days after injection by 19% (P less than .05). Differences in total antibody titers 5 days after injection between temperatures were not significant, but they tended to be reduced by low temperatures. No significant thermal effects on plaque forming cell counts and relative weights (percent of body weight) of spleen and bursa of Fabricius were found. Fat gain during the period between day of injection (Day 0) and peak antibody titers (Day 5) was significantly increased at the low temperatures. Thermal effects on protein gain were not significant, but more protein was deposited at 25 C than at the other temperature regimens during this period after injection.

Animals↗

Changes in brain temperature and free amino acids in normal and protein deprived suckling rats exposed to room temperature.

Previous reports on early-induced protein-calorie malnutrition (PCM) in rats have indicated alterations in the concentration of free amino acids and of protein synthesis in the brain. Recently it was shown that early-induced protein deprivation (PD) retards the development of thermoregulation. This resulted in a failure to maintain a normal rectal temperature after short exposure to room temperature (+22 degrees C) still at the age of 20-25 days corresponding to changes seen in normal rats at an age of 10-15 days. In the present study, 20-day old PD and normal rats where examined with regard to the effect of exposure to room temperature on brain temperature and on brain free amino acids. The results show a similar reduction in brain and rectal temperature of the PD rats occurring within 30 minutes after exposure to room temperature. The reduction was in the range of 5 degrees C. PD rats kept in room temperature for 5 hours and then allowed to recover at 32.5 degrees C showed a slow increase in brain and rectal temperature but normal temperatures were not reached even after 1 hour. The concentration of free amino acids in the brain was examined in rats kept for 1 hour at room temperature or at 32.5 degrees C. In the PD rats kept at 32.5 degrees C, free aspartate and glutamate were reduced whereas taurine, GABA and glycine were increased as compared to their corresponding control rats. As a result of the reduced brain temperature in PD rats exposed to room temperature there was a reduction in free asparagine.(ABSTRACT TRUNCATED AT 250 WORDS)

Amino Acids↗

Temperature-mediated processes in teleost immunity: differential effects of in vitro and in vivo temperatures on mitogenic responses of channel catfish lymphocytes.

The in vitro mitogenic responses of channel catfish peripheral blood leucocytes to ConA and LPS were differentially affected by both in vitro and in vivo temperatures. The magnitude of the response to LPS was relatively independent of both in vitro culture temperature and in vivo acclimation temperature. The magnitude of the response to ConA was suppressed at lower in vitro temperatures although this suppression could be reduced by lower in vivo acclimation temperatures. In vitro temperature-shift experiments indicated that channel catfish PBL could respond to ConA at a lower in vitro temperature if first stimulated with ConA at a higher in vitro temperature. The converse, however was not true in that channel catfish PBL did not respond at a higher in vitro temperature after an initial stimulation with ConA at a lower in vitro temperature. This latter failure to respond could not be attributed to the induction of a suppressor cell (or factor) by exposure to ConA at a lower temperature. These studies, when coupled with other available data on channel catfish PBL subpopulations, are interpreted as supporting the hypothesis that low temperature immunosuppression in fish may result from preferential inhibitory effects on T cells rather than B cells.

Animals↗

Effect of composite temperature on in vitro intrapulpal temperature rise.

OBJECTIVES: To measure in vitro intrapulpal temperature when placing and restoring with either room-temperature or pre-heated (54 and 60 degrees C) composite. METHODS: A K-type thermocouple was placed in the pulpal chamber of an extracted, human bifurcated upper premolar which had a Class V preparation (1 mm remaining dentin thickness) on the facial surface. Tooth roots were immersed in a thermostatically controlled water bath and perfused with water at 1.25 microl/min to simulate physiological circulation in the pulp chamber. The thermocouple was connected to an analog-to-digital converter. The preparation was filled using composite either at room-temperature, or pre-heated to 54 or 60 degrees C with a commercial compule heater (Calset), using standard clinical procedures by one person while continuously monitoring intrapulpal temperature (n=5). Temperature rise over baseline values were determined at various stages during the restoration process: composite placement, contouring, prior to light-curing, and immediately after light-curing (20s, Optilux 501). At each measurement interval, intrapulpal temperature values were compared using ANOVA and the Tukey-Kramer post hoc test (alpha=0.05). RESULTS: Significant differences were found in intrapulpal temperature when comparing pre-heated and room-temperature composite treatments with respect to baseline among the stages of the restorative process. However, the extent of this increase with heated composite was only 0.8 degrees C. A 5 degrees C intrapulpal temperature rise was seen for all groups during photopolymerization. SIGNIFICANCE: Use of pre-heated composite only mildly increased intrapulpal temperature values when compared to composite delivered at room-temperature in an in vitro test environment. The largest temperature change occurred with application of the curing light.

Acrylic Resins↗

Acclimation to the growth temperature and the high-temperature effects on photosystem II and plasma membranes in a mesophilic cyanobacterium, Synechocystis sp. PCC6803.

High-temperature effects on Photosystem II and plasma membranes, temperature dependence of growth, and acclimation to the growth temperature were studied in a mesophilic cyanobacterium, Synechocystis sp. PCC6803. The following results were obtained. (1) Small but distinct temperature acclimation of the PSII reaction center activity was shown for the first time when the activity was measured at inhibitory high temperatures. However, the reaction center activity showed no apparent acclimation when it was measured at growth temperatures after heat stress. (2) Oxygen-evolving activity and the permeability of plasma membranes showed higher resistance to heat when PCC6803 cells were grown at higher temperatures. (3) Acclimation of photosynthesis to the growth temperature seemed to occur so as to maintain photosynthesis activity not at a maximum level but in a certain range at the growth temperatures. (4) Neither sensitivity to high-temperature-induced dissociation of phycobilisomes from the PSII reaction center complexes nor degradation of phycocyanin were altered by changes in the environmental temperature. (5) A close relationship between the viability of cells and the structural changes of plasma membranes (but not the inactivation of photosynthesis) was observed. The denaturation process of PSII complexes and the relationship between the temperature dependence of the growth of Synechocystis PCC6803 cells and that of the photosynthetic activity are also discussed.

Cell Membrane↗

Effects of internal conductance on the temperature dependence of the photosynthetic rate in spinach leaves from contrasting growth temperatures.

The photosynthetic rate may be strongly limited by internal conductance from the intercellular airspace to the chloroplast stroma (g(i)). However, the effects of growth and leaf temperature on g(i) are still unclarified. In this work, we determined the temperature dependence of g(i) in spinach leaves grown at 30/25 degrees C (high temperature; HT) and 15/10 degrees C (low temperature; LT), using the concurrent measurements of the gas exchange rate and stable carbon isotope ratio. Moreover, we quantified the effects of g(i) on the temperature dependence of the photosynthetic rate. We measured g(i) and the photosynthetic rate at a CO(2) concentration of 360 microl l(-1) under saturating light (A(360)) at different leaf temperatures. The optimum temperature for A(360) was 28.5 degrees C in HT leaves and 22.9 degrees C in LT leaves. The optimum temperatures for g(i) were almost similar to those of A(360) in both HT and LT leaves. There was a strong linear relationship between A(360) and g(i). The photosynthetic rates predicted from the C(3) photosynthesis model taking account of g(i) agreed well with A(360) in both HT and LT leaves. The temperature coefficients (Q(10)) of g(i) between 10 and 20 degrees C were 2.0 and 1.8 in HT and LT leaves, respectively. This suggests that g(i) was determined not only by physical diffusion but by processes facilitated by protein(s). The limitation of the photosynthetic rate imposed by g(i) increased with leaf temperature and was greater than the limitation of the stomatal conductance at any temperature, in both HT and LT leaves. This study suggests that g(i) substantially limits the photosynthetic rate, especially at higher temperatures.

Carbon Dioxide↗

Esophageal and tympanic temperature responses to core blood temperature changes during hyperthermia.

Esophageal, rectal, tympanic, and central blood temperature, i.e., pulmonary artery and aortic arch, were recorded in three patients during iatrogenic whole-body hyperthermia for the treatment of advanced malignant metastatic cancer. Aortic temperature closely followed changes in pulmonary arterial temperature, with an average delay time of 27 s. Esophageal temperature reflected quantitatively and more quickly (avg lag time, 80 s) the temperature changes in the pulmonary artery than tympanic membrane temperature. Tympanic temperature was consistently lower than the blood temperature of the heart during steady state. Therefore it is suggested that esophageal temperature is a preferable index of central blood temperature. Additionally, measurement of esophageal temperature can be made more easily and safely than tympanic membrane temperature.

Adult↗

Epidural temperature and possible intracerebral temperature gradients in man.

Although it has been known for a long time that pronounced hypothermia has a protective effect on the brain during ischemia, and that severe hyperthermia damages neuronal tissue, knowledge of human brain temperature is very limited. The recent findings by two independent research groups, that even small differences in brain temperature significantly influence the degree of neuronal damage following cerebral ischemia, became the incentive for measuring brain temperature in neurosurgical patients. The temperature of the lateral ventricle, epidural space, membrana tympani and rectum were measured with copper-constantan thermocouples. During the implantation of an intraventricular catheter for measuring intracranial pressure, a temperature gradient of 0.4-1.0 degrees C between the lateral ventricle and the epidural space was noted. Continuous measurements for 1-5 days showed that the rectal temperature usually adequately reflects the temperature of the epidural space, although the temperature of the membrana tympani followed changes in epidural temperature more closely. However, at times, and in one patient during most of the time, the temperature of the epidural space was up to 1 degree C above rectal temperature. The relevance of these findings for the care of neurosurgical patients is discussed in relationship to what is known about brain temperature from animal experiments.

Adolescent↗

Jugular bulb temperature compared with non-invasive temperatures and cerebral arteriovenous oxygen saturation differences during open heart surgery.

Limited information is available about the correlation between cerebral temperature and routine temperature measurements during cardiopulmonary bypass in infants. Nasopharyngeal, tympanic membrane and rectal temperatures were compared with jugular bulb temperature in ten infants operated on with moderate or deep hypothermia. The cerebral arteriovenous saturation differences were correlated with the temperatures at the four measurement sites. The jugular bulb and nasopharyngeal temperatures showed the most rapid response during cooling and rewarming. The tympanic temperature response varied in an unpredictable way. Rectal temperature, which was the target for rewarming, lagged behind during both cooling and rewarming. Overwarming at the end of cardiopulmonary bypass, seen as jugular bulb and nasopharyngeal temperatures exceeding 38 degrees C, was common after deep hypothermia. A high correlation was found between the cerebral arteriovenous oxygen saturation differences and the jugular bulb temperature (r = 0.81) and the nasopharyngeal and the tympanic temperature (r = 0.79), whereas the correlation with rectal temperature was weaker (0.66).

Body Temperature↗

[Differences in the mechanisms of low-temperature and high-temperature processes in the formation of 3,4-benzopyrene during wood pyrolysis].

In 4 series of experiments a dependence between 3,4-benzpyrene (BP) output and the temperature of fir sawdust pyrolysis under isothermic conditions has been investigated. The experimental series differed in the duration of wood pulp particles stay in the reaction zone (tau). Also EPR spectra of pyrolysis products have been recorded. The experimental series did not differ in an output of ether extract from pyrolysis products, while BP output temperature curves in their shape were found to be largely dependent on tau: with an increased tau these curves definitely showed the maximum in the range of 300-350 degrees C and the BP output raised in the range of this maximum and also at the temperature of 600 degrees C. In the temperature range over 350 degrees C the character of dependence of the EPR signal value on temperature would correlate well with the temperature-dependent BP output, in the range of lower temperatures the EPR signal was not detected. The data obtained are considered as an evidence of two processes of BP formation in wood pyrolysis-a high-temperature process (temperature over 500 degrees C) and low-temperature one (300-350 degrees C). The high-temperature process seems to have the free-radical mechanism of BP formation, whereas in low temperatures it is evidently the result of a ion type reaction.

Benzopyrenes↗

The effect of ambient temperature extremes on tympanic and oral temperatures.

Exposure to ambient temperature extremes immediately preceding emergency department triage may affect tympanic membrane temperatures taken with infrared emission detection thermometers. In a prospective, unblinded study, 20 healthy subjects, on 2 separate days, underwent 15-minute exposures to hot (43.5 degrees C) and cold (-5 degrees C) temperature extremes in an environmental control room (ECR). Tympanic and oral temperatures were taken at baseline and at 2-minute intervals for 20 minutes after exiting the ECR. Rectal temperatures remained stable during the exposures. Oral temperatures rose significantly after hot exposure (P less than .05; max 0.4 degrees C) and briefly decreased after cold exposure (max 0.5 degrees C). Tympanic temperatures were elevated for 20 minutes after hot exposure (max 0.8 degrees C) and decreased briefly only in male subjects after cold exposure (max 0.7 degrees C). Individuals demonstrated wide variability in their temperature responses. Tympanic and oral temperatures taken within the first 20 minutes after exposure to outdoor temperature extremes may fail to accurately reflect the patient's true temperature.

Adult↗

Mechanical behavior at different temperatures and stresses for superelastic nickel-titanium orthodontic wires having different transformation temperatures.

OBJECTIVE: The purpose of this study was to investigate the mechanical properties of superelastic nickel-titanium orthodontic wires under controlled stress and temperature. METHODS: Three different superelastic nickel-titanium wires were examined using differential scanning calorimetry (DSC), three-point bending test and micro X-ray diffraction (micro-XRD). The three-point bending test was carried out at constant temperature (23, 37 and 60 degrees C) and stepwise temperature changes (37-60 degrees C and to 37 degrees C) (37-2 degrees C and to 37 degrees C). Five specimens of each wire were tested. Micro-XRD spectra were measured at the tension side of the wire when the temperature changed from 37 to 60 degrees C or 2 degrees C. RESULTS: The load during the stepwise temperature changes (37-2 degrees C and to 37 degrees C) was consistent with that measured at a corresponding constant temperature. The micro XRD spectrum clearly showed that the austenite phase was transformed to martensite phase when the temperature is decreased from 37 to 2 degrees C. In a stepwise temperature change (37-60 degrees C and to 37 degrees C), the load became higher than the original load at each corresponding constant temperature. However, there was no detectable change in the micro-XRD spectrum when the temperature was increased from 37 to 60 degrees C. SIGNIFICANCE: The superelastic nickel-titanium wires exhibited complicated and unexpected mechanical properties under stepwise temperature change. This study shows the possibility of qualitative analysis using micro-XRD to understand mechanical properties of these nickel-titanium wires.

Calorimetry, Differential Scanning↗