Effects of exogenous glucose or colostrum on body temperature, plasma glucose, and serum insulin in cold-stressed, newborn Brahman calves.

The effects of ambient temperature and source of exogenous energy (glucose or colostrum) on the ability of newborn Brahman calves to maintain rectal temperature (RT) were determined. All calves were removed from dams within 30 min of birth, before suckling. Calves were catheterized and placed in either a warm (25 degrees C) or cold (5 degrees C) environment for 150 min and given either colostrum or glucose. This resulted in four groups (warm colostrum, n = 7; cold colostrum, n = 7; warm glucose, n = 6; cold glucose, n = 6). Blood samples and RT were obtained at 15-min intervals during warm or cold through 150 min, when calves were removed from cold, and at 180, 240, and 300 min. After 60 min, each calf was given either 1 L of colostrum (38 degrees C) from its dam or glucose (38 degrees C) infusion of 750 mg/kg BW. Plasma glucose concentrations were determined by enzymatic techniques and serum insulin concentrations by RIA. Calves exposed to cold or warm air temperatures had similar declines in rectal temperature from 0 to 60 min. Colostrum-fed, cold calves had a greater (P less than .07) decrease in RT than did colostrum-fed, warm calves from 75 through 150 min; glucose-infused warm and cold calves had intermediate decreases in RT. Plasma glucose increased (P less than .0001) in glucose-infused compared with colostrum-fed calves at 75 min, but glucose-infused calves had lower (P less than .02) glucose levels from 180 to 300 min. Higher (P less than .05) glucose concentrations     

Consequences of short term fluctuations of the environmental temperatures in calves--Part 2: Effects on the health status of animals within three weeks after exposure

The aim of the present study was to examine consequences of sudden changes in ambient temperature over a 4-hour period (see part 1 [ELMER & REINHOLD, 2002]) on respiratory health in clinically healthy calves. Therefore, the relationship between short-term changes in ambient temperature and the occurrence of clinical respiratory disease was checked over a period of 3 weeks after exposure in 10 calves exposed to 5 degrees C, in 9 calves exposed to 35 degrees C and in 8 control calves (kept at 18-20 degrees C). Within the period beginning 3 days before exposure and lasting until up to 21 days after exposure, each calf was examined clinically. Rectal temperature and respiratory rate were measured daily. All calves were euthanised on day 21 after exposure. Macroscopically visible pneumonic lesions were evaluated using a semiquantitative system. Tissue samples from tonsils, bronchi, trachea, lung and mediastinal lymph nodes were examined bacteriologically. In contrast to non-exposed control calves, severe respiratory illness was observed in individual calves of both exposed groups (5 degrees C, 35 degrees C). Significant increases in body temperature, respiratory rate and animal losses (2 calves died in the group exposed to 5 degrees C, one calf died in the group exposed to 35 degrees C) were the main clinical findings. At necropsy (3 weeks after exposure), no pneumonic lesions were observed in control calves--despite the fact that this group had the highest microbiological colonisation rates in tonsils and in large airways, i.e. trachea and bronchi, within all groups. However, variable pneumonic lung lesions were seen in remaining calves exposed to cold or warm air (5 degrees C, 35 degrees C). The microbiological examination confirmed that mainly Mycoplasma spp. were identified in the lung tissue of calves exposed to 5 degrees C while Pasteurella multocida and/or Mannheimia haemolytica were the only germs found in the lung tissue of calves exposed to 35 degrees C. The results of parts 1 and 2 of the present study related to health issues of calves should be taken into account for future legislation on animal welfare.     

Physiological responses of newborn Bos indicus and Bos indicus x Bos taurus calves after exposure to cold

Brahman (n = 9) and 1/2 Simmental x 1/4 Brahman x 1/4 Hereford (n = 11) calves were utilized to determine the influence of exposure to cold on the physiology of the neonate. All calves were removed from their dams within 20 min of birth and prior to suckling. Calves were assigned randomly within breed to either a warm (W; 31 degrees C) or cold (C; 4 degrees C) environmental treatment group. Jugular blood samples were collected via indwelling catheters at 20-min intervals for 180 min. At 100 to 120 min of sampling, all calves were given 1.2 liters of colostrum from their dams via stomach tube. At 120 min, C calves were placed in the W environment. Calf vigor score (CVS) and rectal temperature were determined at each time blood was collected. Serum or plasma was analyzed for glucose (GLU), lactate (LAC), blood urea nitrogen (BUN), hemoglobin (HEM), triglyceride (TRG), triiodothyronine (T3), thyroxine (T4), insulin (INS), cortisol (CORT) and nonesterified fatty acid (NEFA) concentration. Rectal temperature was lower (P less than .01) in C Brahman than in W Brahman and C or W crossbred calves. Crossbred calves had higher (P less than .01) CVS than Brahman calves. Calves in W had lower (P less than .01) GLU than C calves. Brahman calves had higher GLU, LAC, BUN, TRG, T3, T4 and CORT (P less than .05) than crossbred calves. The C Brahman calves had the highest (P less than .05) TRG, CORT, T3 and T4 of all groups. Concentration of NEFA were higher (P less than .01) in C than in W calves.(ABSTRACT TRUNCATED AT 250 WORDS)     

Sympathoadrenal and adrenal hormonal responses of newborn calves to hypothermia.

Seventeen newborn Holstein-Friesian bull calves were cold-stressed by total body immersion in water at 15 to 17 degrees C until the core body temperature was lowered by 10 degrees C. Nine additional calves (noncold-stressed) were immersed in water at 35 to 37 degrees C. Eight of the cold-stressed calves were euthanatized soon after removal from the water while the others (n=9) were allowed to recover in a cold room at 4 degrees C for 72 hours. Noncold-stressed calves were kept at 25 degrees C for 72 hours. Sympathoadrenal an adrenal hormonal responses of calves were determined by analysis of plasma for glucose, corticosteroids, and catecholamines. Plasma concentration of glucose and corticosteroids rapidly increased in cold-stressed calves soon after immersion and remained higher (P less than of equal to 0.05) than concentrations in noncold-stressed calves during immersion and most of recovery. There was a threefold increase (P less than or equal to 0.05) in concentration of catecholamines in plasma of cold-stressed calves and only a slight increase in noncold-stressed calves during immersion. Catecholamine concentrations remained elevated in cold-stressed calves during most of recovery. Results provide direct evidence that sympathoadrenal and adrenal hormonal responses to cold are well developed in newborn calves and that changes in concentrations of glucose, corticosteroids, and catecholamines in plasma of these animals are sensitive indicators of their ability to respond to cold stress.     

Effects of feeding supplemental fat to beef cows on cold tolerance in newborn calves

Our objectives were to examine the effects of added fat in late-gestation cow diets on neonatal response to cold. In Exp. 1, pregnant fall-calving heifers received control (n = 5), safflower seed (n = 5), or whole cottonseed (n = 5) diets. The hay-based, isonitrogenous, and isocaloric diets, fed for 47 d prepartum, contained 1.5, 4.0, and 5.0% fat for control, safflower, and whole cottonseed diets, respectively. At calving, calf BW and vigor score, as well as fat, lactose, and IgG in colostrum were not affected (P > 0.30) by diet. Heifers fed the safflower diet tended to have greater colostral solids (P < 0.10) than heifers fed the control or whole cottonseed diets. At 6.5 h of age, calves were placed in a 5 degrees C cold room for 90 min. Calf vigor, shivering, body temperature, and blood samples were taken every 15 min. During cold stress, calf body temperature decreased 0.7 degrees C (P < 0.03). Across all diets, shivering and serum glucose concentrations increased (P < 0.05), whereas calf vigor and cortisol concentrations decreased (P < 0.02) during cold exposure. In Exp. 2, pregnant spring-calving cows (n = 98) received a control (n = 47) or whole cottonseed (n = 51) supplement. Hay-based diets fed for 68 d prepartum contained 2.0 and 5.0% fat for control and whole cottonseed diets, respectively. Calf BW, vigor, shivering, dystocia score, time to stand, time to nurse, serum glucose concentrations, and serum IgG were not affected (P > 0.50) by diet. Between 30 and 180 min, body temperature of calves from dams fed the whole cottonseed supplement decreased (P < 0.05) more than calves from dams fed the control supplement. Serum glucose concentrations in calves were not affected by diet (P > 0.30). Serum cortisol concentrations tended (P < 0.09) to be greater for calves from dams fed whole cottonseed than control calves. When ambient temperature was < 6 degrees C, calves born to dams fed whole cottonseed had greater (P < 0.05) BW, tended (P < 0.1) to stand earlier, and had greater serum IgG concentrations. We conclude that calves from dams fed high-fat diets containing safflower or whole cottonseed respond similarly to cold stress, but these responses may not be consistent with greater cold resistance. In addition, high-fat dietary supplementation of late-gestation cows may only be beneficial during calving seasons with prolonged cold weather.     

Some observations on the effects of age of calves on the phagocytosis and killing of Staphylococcus aureus by polymorphonuclear leucocytes

The effects of age on bovine polymorphonuclear (PMN) cell function were investigated by comparing the efficiencies of phagocytosis and killing of Staphylococcus aureus by peripheral blood leucocytes sequentially obtained from 15 calves between the ages of less than 1 and 84 days. One group of seven calves was kept in a controlled environmental chamber with air temperature of 5 degrees C and 58% relative humidity (RH) and another group of eight calves was kept at 16 degrees C and 58% RH. The calves were given a diet a liquid milk substitute and dry food, and were weaned abruptly from the liquid diet at 35 days of age. The in-vitro efficiencies of phagocytosis, and of killing, Staphylococcus aureus by peripheral blood leucocytes were similar for calves in air temperatures of 5 degrees C and 16 degrees C (P greater than 0.05). Peripheral blood leucocytes obtained from calves of less than 1 day of age were more efficient in phagocytosing S. aureus than those obtained when the same calves were 14-84 days of age (P less than 0.001). Peripheral blood leucocytes obtained when the calves were 42 and 56 days of age were significantly less efficient in phagocytosing and killing S. aureus than those obtained when the same calves were less than 1, 14, 28, 70 and 84 days of age (P less than 0.001).     

Pulmonary particle deposition and airway mucociliary clearance in cold-exposed calves.

Effect of cold-induced changes in respiratory pattern on pulmonary particle deposition was investigated in 10 male Holstein calves between the ages of 1 and 3 months. Deposition of intranasally instilled fluorescence-enhanced Pasteurella haemolytica was significantly higher (P less than 0.05) for cold-exposed calves and appears to be caused by the cold-induced respiratory pattern change. Deposition was greater in apical and mediastinal lung lobes, but the reason for this preferential deposition is uncertain. Nasal mucus velocity was measured in 4 nonanesthetized calves at ambient temperature of 2 to 4 C and 16 to 18 C, using tantalum-paraffin oil droplets and serial radiography. Nasal mucus velocity was 24% lower during cold exposure. In addition, the effect of mucosal temperature on tracheal mucus velocity was determined in excised tracheas from 7 calves. A direct relationship existed between mucosal temperature and tracheal mucus velocity within the mucosal temperature range studied (35.0 to 39.5 C). Tracheal air temperature measurements in calves at ambient temperatures of -10.4 C (n = 4) and 18.5 C (n = 5) indicated that conditioning of inspired air is not complete at the tracheal level during extreme cold exposure. Therefore, cold air may directly influence tracheal mucociliary clearance. It is speculated that cold exposure increases pulmonary deposition of pathogens, while simultaneously decreasing mucociliary clearance of the upper airways, thus predisposing cold-exposed calves to respiratory tract infection.     

Physiological responses of Bos taurus and Bos indicus cattle to prolonged, continuous heat and humidity

Two experiments were conducted to investigate the physiological responses of Bos taurus (Angus cross, n = 6) and Bos indicus (Brahman, n = 6) cattle to prolonged heat and humidity, as can occur during live export by sea. Each experiment was carried out in climate-controlled rooms, where heifers were exposed to 15 d of sustained heat and humidity. The treatment was designed to be representative of a long-haul, live-export voyage leaving a southern Australian winter and traveling to a Middle Eastern summer. Wet bulb temperature (WBT) was used to give a combined measure of dry bulb temperature and relative humidity and was increased over several days, culminating in 5 d at 32 degrees C WBT between d 7 and 11. By d 11, the respiratory rate and core body temperature increased (P < 0.001) compared with values at lower ambient temperature on d 1 and 2 when climate-controlled rooms were not operating. Feed intake of Bos taurus was reduced (P < 0.001) by d 11, whereas that of Bos indicus did not change (P = 0.14). Despite no diurnal variation in climatic conditions, core body temperature of both Bos taurus and Bos indicus continued to show a circadian amplitude of approximately 1 degrees C throughout the hottest period. This amplitude increased during the recovery period after heat was removed (up to 1.8 degrees C for Bos indicus and 1.6 degrees C for Bos taurus). Water intake for both Bos taurus and Bos indicus increased when WBT increased (P < 0.01 on d 11). Significant acid-base and blood electrolyte imbalances occurred in both Bos taurus and Bos indicus, with changes in Bos taurus being more substantial and prolonged. The increase in respiratory rate coincided with a decrease in the partial pressures of carbon dioxide and bicarbonate in venous blood. However, during the hottest period, average daily venous blood pH remained unchanged. When the heat load was reduced after d 11, the blood pH decreased, indicating metabolic acidosis. Blood pH declined from 7.44 to 7.36 for Bos taurus (P < 0.001) and from 7.44 to 7.38 for Bos indicus (P < 0.001). Other parameters measured include heart rate; packed cell volume; plasma and urine Na, K, and Cl; urine pH; and specific gravity. Our results suggest that Bos taurus cattle experience significant physiological changes during exposure to prolonged and continuous high heat and humidity, with alterations persisting for some days after the heat-stress conditions subside. Bos indicus experience similar but less pronounced physiological changes.     

Histological features of respiratory epithelium of calves held at differing temperature and humidity.

The effect of ambient temperature and humidity on the structure of respiratory epithelium of calves was studied. Four calves of each of three experiments were acclimatized to a nonoperational environmental chamber for six days and then exposed to constant extremes of temperatures and relative humidity of one of 30 degrees C --35%, or 27 degrees C--92%, or 5 degrees C--92% respectively in this chamber for eight days each. Five calves (3 and 2) were similarly acclimatized then exposed to 1 degrees C--40%. Nasal swabs were taken from all animals at regular intervals. Swabs of three animals yielded Mycoplasma spp. and one swab yielded the virus of infectious bovine rhinotracheitis. Detailed histological studies of respiratory epithelium of nose, trachea, major bronchus and terminal bronchioli were conducted at four sites. Goblet cells were least in calves held in hot and dry air; calves held in dry air had the least polymorphonuclear cells and the greatest prevalence of hypochromatic cell layers and vacuolation of epithelial cells. Differences between experiments were evident most for sites of trachea and major bronchus.     

Response to environmental temperatures in Brahman calves during the first compared to the second day after birth.

Brahman calves (n = 28) were used to evaluate the effect of environmental temperature during the 1st or 2nd d after birth. Calves were removed from their dams within 30 min of birth (newborn; D0) before suckling or at 20 h of age and fasted for 4 h before treatment (day-old; D1). Calves were placed in either a warm (W; 25 degrees C) or a cold (C; 5 degrees C) environment for 2 h and either maintained in or transferred to, respectively, W for 22 h. Blood samples were collected via jugular catheters at 15-min intervals beginning at initial placement in W or C through 3 h and at 4, 5, 6, 8, 10, 12, 14, 18, and 24 h. Rectal temperature (Tr) was recorded with each sample. Following the 60-min and 12-h samples, each calf was administered 1 liter of colostrum from its dam. Serum or plasma was analyzed for glucose, lactate, plasma urea nitrogen, triglycerides, nonesterified fatty acids, insulin, cortisol, triiodothyronine (T3), and thyroxine (T4). Rectal temperature of D0C calves was lower (P less than .05) than that of other calves from 75 min through 3 h. Insulin, lactate, T3, and plasma urea nitrogen concentrations were not different among all calves. Higher (P less than .01) cortisol and T4 concentrations were observed in D0 than in D1 calves. Cortisol (P less than .008) and nonesterified fatty acid (P less than .05) levels were greater in C than in W calves. All D0 calves had lower (P less than .0001) glucose concentrations than D1 calves until the 12-h feeding.(ABSTRACT TRUNCATED AT 250 WORDS)     

The effects of cold stress on neonatal calves. I. Clinical condition and pathological lesions.

Newborn Holstein-Friesian calves were cold stressed by immersion in water at 15 to 17 degrees C until the core body temperature was lowered by 10 degrees C. Non-cold stressed calves were immersed in water at thermoneutral temperature (35 to 37 degrees C). The time required to lower the core body temperature of the cold stressed calves by 10 degrees C was 172 +/- 87 minutes (mean +/- SD). The time required for the core body temperature of the cold stressed calves to return to normal after immersion was 400 +/- 140 minutes (mean +/- SD). Differences were observed between cold and noncold stressed calves in the shivering response during immersion and the clinical condition after immersion. Cold-induced pathological lesions were confined to tissues located peripherally, particularly in the hind legs. Significant differences were observed between cold and noncold stressed calves in the incidence of subcutaneous edema in the ventral sternum (P less than or equal to 0.025), subcutaneous hemorrhage in the hind legs (P less than or equal to 0.025), synovitis (P less than or equal to 0.025) and hemorrhage (P less than or equal to 0.05) of the synovial membranes of the hock joints and hemorrhage (P less than or equal to 0.05) into the hock joint cavities.     

Seasonal comparisons of anthelmintic activity of levamisole pour-on in cattle in the USA

Anthelmintic activity of a pour-on formulation of levamisole, applied during warm weather (16 degrees to 36 degrees C) at 10 mg/kg bodyweight, was evaluated in groups of naturally parasitised calves. This activity was compared to that obtained in similar groups of calves treated in the winter (-4 degrees to +7 degrees C). Controlled efficacy of the pour-on formulation was determined for each season by comparing mean worm burdens in treated calves sacrificed seven to nine days after treatment to non-treated controls. In these trials, burdens of Bunostomum phlebotomum, Cooperia species, Haemonchus placei, Nematodirus species, Oesophagostomum radiatum, Ostertagia ostertagi and Trichostrongylus axei in treated calves were reduced by 83.3 to 100 per cent in the summer and 89.2 to 100 per cent in the winter. Field investigations at nine locations across the USA compared changes in faecal egg counts for cattle treated and evaluated during warm summer months (27 degrees to 36 degrees C) to those treated during cold winter months (-18 degrees to +10 degrees C). Overall, faecal egg counts were reduced by 90.2 per cent in the summer trials and 94.0 per cent in the winter trials. The results of these trials indicate that there is no seasonal variation in the anthelmintic activity of this pour-on formulation of levamisole.     

Survey of transport environments of circus tigers (Panthera tigris).

The type of equipment used to transport circus tigers, environmental factors experienced during transport, and resultant body temperatures of tigers transported were surveyed during hot and cold weather conditions with six different circus tiger acts. Dataloggers recorded interior and exterior temperatures, relative humidity, and radiant heat at 5-min intervals during each trip. Microdataloggers fed to the tigers recorded body temperature and were recovered from eight Bengal (Panthera tigris tigris), Siberian (P. t. altaica), or Bengal-Sumatran (P. t. tigris-P. t. sumatrae) cross tigers from four different circuses. Three basic types of systems were used by circus acts to transport tigers: freestanding cages mounted on wheels that were winched or pushed into a semitrailer for transport, cages built into the trailer itself, and weather-resistant units transported on flatbed railcars or flatbed truck trailers. The highest temperature encountered inside a trailer was 37.3 degrees C in hot weather conditions, but overall, temperatures were usually between 21.1-26.7 degrees C. Temperature inside the trailers did not appear to be affected by movement and did not generally exceed ambient temperatures, indicating adequate insulation and passive ventilation. During cold weather trips, the lowest temperature inside the trailers was -1.1 degrees C, occurring during an overnight stop. Interior temperatures during cold weather transport stayed 2-6 degrees C warmer than ambient temperatures. The body temperatures of the tigers were unaffected by extreme temperatures. The only changes observed in body temperature were increases of 1-2 degrees C caused by activity and excitement associated with loading in several groups of tigers, regardless of whether it was hot or cold weather. Whenever measured, carbon monoxide and ammonia were below the detectable concentrations of 10 and 1 ppm. respectively. Overall, transport did not appear to have any adverse effects on the tigers' ability to thermoregulate.     

The effect of high environmental temperatures on fattening performance and growth of boars

Fifty-eight boars of the “German Landrace” breed were fattened between 70 and 110 kg in individual housing at ambient temperatures of 15°C or 35°C with 60% relative humidity in both cases.The animals under warm conditions showed increased growth of the skeleton and reduced growth of the heart, liver, kidneys, spleen and stomach.The feed intake was strongly restricted by the high temperature, while water consumption showed an extremely high variance. Correspondingly the daily gains were strongly depressed, although the feed conversion ratios of the warm- and cold-housed animals were not significantly different. The fat thickness of the warm-housed animals was significantly lower.     

Metabolic heat production of neonatal calves during hypothermia and recovery

Metabolic heat production and rectal temperature were measured in 19 newborn calves (41.8 +/- 3.7 kg) during hypothermia and recovery when four different means of assistance were provided. Hypothermia of 30 degrees C rectal temperature was induced by immersion in 18 degrees C water. Calves were rewarmed in a 20 to 25 degree C air environment where thermal assistance was provided by added thermal insulation or by supplemental heat from infrared lamps. Other calves were rewarmed by immersion in warm water (38 degrees C), with or without a 40-ml drench of 20% ethanol in water. Resting (prehypothermia) and cold-induced summit metabolism of the calves was 2.5 +/- .1 and 8.2 +/- .22 W/kg and occurred at rectal temperatures of 39.5 +/- .06 and 36.2 +/- .26 degrees C, respectively. During cooling, metabolic heat production declined at the rate of .65 W/kg per degrees C decline in rectal temperature. The time required to regain euthermia from a rectal temperature of 30 degrees C was longer for calves with added insulation and those exposed to heat lamps than for the calves in the warm water and warm water plus ethanol treatments (90 and 92 vs 59 and 63 +/- 6.4 min, respectively). During recovery, the calves rewarmed with the added insulation and heat lamps produced more heat metabolically than the calves rewarmed in warm water. Total heat production during recovery was 34.1, 31.1, 18.3, 16.9 +/- 1.07 kJ/kg for the calves with added insulation, exposed to the heat lamps, in warm water and in warm water plus an oral drench of ethanol, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)     

Clinical, cardiopulmonary and haemocytological effects of xylazine in goats after acute exposure to different environmental temperature and humidity conditions

This study was carried out to assess the influence of xylazine administration on clinical, cardiopulmonary and haemocytological variables after acute exposure to different environmental conditions. Xylazine hydrochloride was administered intravenously at 0.1 mg/kg body mass to 6 clinically healthy, castrated male goats. All animals were exposed for 60 min to 3 sets of climatic conditions: 14 degrees C, 33% relative humidity; 24 degrees C, 55% RH, and 34 degrees C, 65% RH. The variables that were measured for a period of 60 min after xylazine administration were sedation, analgesia, salivation, urination, ventilation rate, heart-rate, mean arterial blood pressure, oesophageal temperature, haematocrit, mean corpuscular volume and mean corpuscular haemoglobin concentration. Xylazine induced sedation, analgesia, salivation and urination independently of the 3 environmental conditions. Environment had no influence on the onset, duration and recovery from sedation. In the 14 degrees C environment, xylazine resulted in a significant decrease in ventilation and heart-rate from baseline values. Significant changes in mean arterial blood pressure, haemoglobin concentration, mean corpuscular volume, haematocrit and red cell count were observed in the 3 environments. Total plasma protein was significantly altered at 24 degrees C and 34 degrees C. Acute exposure of goats to different environmental conditions had no significant influence on the clinical, cardiopulmonary and haemocytological variables. Physiological changes induced by xylazine were therefore independent of the environment.     

The use of a medetomidine, butorphanol and atropine combination to enable blood sampling in young pigs

AIM: To determine the suitability of a reversible, injectable anaesthetic combination including medetomidine, butorphanol and atropine to produce the degree of immobilisation required to allow blood sampling in young pigs. METHODS: Twenty 6-week-old crossbred, intact male pigs were sedated with an intramuscular (I/M) injection of 80 microg/kg medetomidine, 200 microg/kg butorphanol and 25 microg/kg atropine. Heart and respiratory rates and rectal temperatures were monitored. Excessive salivation, gagging, laryngeal reflex, presence of pedal reflex and deep and surface analgesia were noted. Time of injection and the time when pigs reached mild and full sedation were also recorded. RESULTS: Mild sedation was produced in 90% of pigs after 5.6 (SEM 0.96) min (n = 18; median 5, range 2-16 min), and full sedation (lateral recumbency and loss of jaw tone) in 60% of pigs after 12.5 (SEM 2.14) min (n = 12; median 10, range 5-28 min). The depth and duration of sedation were very variable and most animals were easily aroused. Ninety percent of the animals required the administration of halothane by mask to allow blood sampling, but the amount of halothane required was small. Heart and respiratory rates decreased (p < 0.001) but remained within the normal range. Rectal temperature was above normal at the time of sedation and at the time of blood sampling when the ambient temperature was 29 degrees C but not when the ambient temperature was reduced to 25 degrees C. CONCLUSIONS: The combination of medetomidine, butorphanol and atropine at these doses produced sedation of variable depth and duration that was insufficient on its own to allow blood sampling in the majority of pigs. Hyperthermia can occur in temperature-controlled environments when using medetomidine, butorphanol and atropine in pigs. Reduction of stress and a quieter environment may improve the effects of the anaesthetic combination.     

Brown adipose tissue development and metabolism in ruminants

We conducted several experiments to better understand the relationship between brown adipose tissue (BAT) metabolism and thermogenesis. In Exp. 1, we examined perirenal (brown) and sternum s.c. adipose tissue in 14 Wagyu x Angus neonates infused with norepinephrine (NE). Perirenal adipocytes contained numerous large mitochondria with well-differentiated cristae; sternum s.c. adipocytes contained a few, small mitochondria, with poorly developed cristae. Lipogenesis from acetate was high in BAT but barely detectable in sternum s.c. adipose tissue. In Exp. 2, we compared perirenal and tailhead adipose tissues between NE-infused Angus (n = 6) and Brahman (n = 7) newborn calves. Brahman BAT contained two-to-three times as many total beta-receptors as Angus BAT. The mitochondrial UCP1:28S rRNA ratio was greater in Brahman BAT than in BAT from Angus calves. Lipogenesis from acetate and glucose again was high, but lipogenesis from palmitate was barely detectable. Tail-head s.c. adipose tissue from both breed types contained adipocytes with distinct brown adipocyte morphology. In Exp. 3, three fetuses of each breed type were taken at 96, 48, 24, 14, and 6 d before expected parturition, and at parturition. Lipogenesis from acetate and glucose in vitro decreased 97% during the last 96 d of gestation in both breed types, whereas the UCP1 gene expression tripled during gestation in both breed types. At birth, palmitate esterification was twice as high in Angus than in Brahman BAT and was at least 100-fold higher than in BAT from NE-infused calves from Exp. 2. Uncoupling protein-1 mRNA was readily detectable in tailhead s.c. adipose tissue in all fetal samples. In Exp. 4, male Brahman and Angus calves (n = 5 to 7 per group) were assigned to 1) newborn treatment (15 h of age), 2) 48 h of warm exposure (22 degrees C) starting at 15 h of age, or 3) 48 h of cold exposure (4 degrees C) starting at 15 h of age. Brahman BAT adipocytes shrank with cold exposure, whereas Angus BAT adipocytes did not. Similarly, BAT from neonatal lambs (Exp. 5; n = 6 per group) was depleted of lipid in response to cold exposure, although UCP1 gene expression persisted. In Exp. 4, NE stimulated lipogenesis from palmitate in BAT incubated in vitro. Lipogenesis from palmitate was higher in Angus than in Brahman BAT, and increased with both warm and cold exposure. These studies suggest that BAT from Brahman calves may be exhausted of lipid shortly after birth during times of cold exposure.     

Effects of prepartum supplementary fat and muscle hypertrophy genotype on cold tolerance in newborn calves.

Effects of feeding pregnant dams supplemental dietary fat during the last 55 d of gestation on cold tolerance of newborn crossbred calves with (Piedmontese cross, P, n = 15) or without (Hereford cross, H, n = 16) the muscle hypertrophy allele was determined. Primiparous F1 dams gestating F2 calves of the respective breeds were assigned randomly within breed to receive gestation diets containing either 2.2 (Low Fat; LF) or 5.1% fat (High Fat; HF). Safflower (Carthamus tinctorius L.) seeds containing 37% oil with 79% linoleic acid were the supplemental fat source in diets formulated to be isocaloric-isonitrogenous. At parturition, calves were separated from their dams, fed 38 degrees C pooled dairy cow colostrum (30 mL/kg BW), muzzled to prevent suckling, and returned to their dams in a heated (22 degrees C) room for 3.5 h. At 4 h of age (birth = 0 h), a catheter was inserted into the jugular vein. At 5 h of age, calves were placed in a 0 degrees C room for 140 min, and rectal temperatures and blood samples were obtained at 10- and 20-min intervals. Blood was assayed for cortisol and glucose. Rectal temperature was affected by diet (P<.05), time, diet x time, and breed x time (P<.01 for time and the interactions). Cortisol and glucose concentrations were not affected by diet, breed, or the diet x breed interaction, but they were affected by time, breed x time (both P<.01), and diet x time (P = .06). Calves from HF dams had higher rectal temperatures than calves from LF dams, and the HF calves maintained higher rectal temperatures throughout cold exposure. Cortisol concentrations were lower (P = .06) in calves from HF dams, and these calves had more (P = .06) glucose available for metabolic heat production than calves from LF dams. Piedmontese-cross calves maintained higher (P<.01) rectal temperatures and had higher cortisol and glucose (both P<.01) concentrations than did H-cross calves. We conclude that feeding dams supplemental fat during late gestation increased heat production in newborn calves and potentially could increase calf survival; calves with muscle hypertrophy may have a different ratio of shivering vs nonshivering thermogenesis due to differences in body composition or relationships among uncoupling proteins.     

Comparison of temperature readings from a percutaneous thermal sensing microchip with temperature readings from a digital rectal thermometer in equids

OBJECTIVE: To compare temperature readings from an implantable percutaneous thermal sensing microchip with temperature readings from a digital rectal thermometer, to identify factors that affect microchip readings, and to estimate the sensitivity and specificity of the microchip for fever detection. DESIGN: Prospective study. ANIMALS: 52 Welsh pony foals that were 6 to 10 months old and 30 Quarter Horses that were 2 years old. PROCEDURES: Data were collected in summer, winter, and fall in groups 1 (n = 23 ponies), 2 (29 ponies), and 3 (30 Quarter Horses), respectively. Temperature readings from a digital rectal thermometer and a percutaneous thermal sensing microchip as well as ambient temperature were recorded daily for 17, 23, and 19 days in groups 1 through 3, respectively. Effects of ambient temperature and rectal temperature on thermal sensor readings were estimated. Sensitivity and specificity of the thermal sensor for detection of fever (rectal temperature, >or= 38.9 degrees C [102 degrees F]) were estimated separately for data collection at ambient temperatures 15.6 degrees C. RESULTS: Mean ambient temperatures were 29.0 degrees C (84.2 degrees F), -2.7 degrees C (27.1 degrees F), and 10.4 degrees C (50.8 degrees F) for groups 1 through 3, respectively. Thermal sensor readings varied with ambient temperature and rectal temperature. Rectal temperatures ranged from 36.2 degrees to 41.7 degrees C (97.2 degrees to 107 degrees F), whereas thermal sensor temperature readings ranged from 23.9 degrees (75 degrees F) to 42.2 degrees C (75 degrees to 108 degrees F). Sensitivity for fever detection was 87.4%, 53.3%, and 58.3% in groups 1 to 3, respectively. CONCLUSIONS AND CLINICAL RELEVANCE: The thermal sensor appeared to have potential use for initial screening of body temperature in equids at ambient temperatures > 15.6 degrees C.