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The site of the calorigenesis observed in birds after glucagon was sought in control and cold-acclimated (CA) ducklings. Twenty-four 6-wk-old muscovy ducklings were reared either at thermoneutrality (TN) (25 degrees C) or in the cold (4 degrees C) from the age of 1 wk. Glucagon-induced calorigenesis (GIC) was estimated at 25 degrees C after a peritoneal glucagon injection (103 nmol/kg). Glucagon induced a higher increase in animal heat production (indirect calorimetry) and body temperature in CA (+45% and +1.1 degrees C) than in control ducklings (+30% and +0.4 degree C). In CA ducklings, the perfusion rate (thermal clearance method) and temperature of gastrocnemius increased (+130% and +1.0 degree C) shortly after glucagon, whereas tissue oxygenation (polarography) decreased (-34%). There was no significant effect of glucagon in TN controls. These changes, which peaked 45-60 min after glucagon injection, indicated a prolonged increase of muscle O2 consumption in CA ducklings. Leg muscle blood flow (radioactive microspheres) measured 45 min after glucagon was slightly increased in controls (+20%; P < 0.05), while in CA ducklings, the increase was larger (+76%; P < 0.05). The arteriovenous difference in O2 content was not markedly affected by glucagon in both groups. These parameters indicated an increase in leg muscle O2 uptake in response to glucagon of +29% in controls and +76% in CA ducklings. In controls, 28% of the GIC measured in vivo could be attributed to whole body skeletal muscles, compared with 53% in CA ducklings. The remaining part might be accounted for mostly by the liver.(ABSTRACT TRUNCATED AT 250 WORDS)

To determine the effects of cold acclimation on the oxidative capacity of different tissues and their possible role in nonshivering thermogenesis (NST) in a desert rodent, the gerbil (Gerbillus campestris), measurements of cytochrome oxidase activity (COX) were performed on homogenates of liver, brown adipose tissue (BAT), and subsarcolemmal (SS) and intermyofibrillar (IMF) fractions of skeletal muscle. Total organ mass was also measured. Gerbils were maintained either at thermoneutrality (TN) or cold [4 degrees C, ambient temperature (Ta)] for 4 (CA4) or 8 (CA8) wk. A comparative study was made with mice (Mus musculus). Total and relative masses of BAT increased significantly in both gerbils and mice during cold acclimation, whereas muscle mass decreased in CA4 gerbils. Specific and total COX (TCOX) increased in the three tissues. A considerable increase (+170%, P less than 0.05) of TCOX and protein content in liver of CA4 gerbils compared with controls was observed, whereas no significant changes occurred in liver of CA4 mice. In muscle, an increase of TCOX in SS and a reduction in IMF cell compartments were noted. The increase in BAT oxidative capacity in CA4 gerbils represented only a small portion of that in liver (36%) and in SS fraction of muscle (41%) at the same stage of acclimation. The ability of the three tissues to contribute to components of thermogenesis in vivo was evaluated. The sum of oxidative capacity of the three tissues was largely above the peak metabolic rate (PMR), whereas that of muscle exceeded maximum shivering thermogenesis, which developed both in TN and CA4 gerbils.(ABSTRACT TRUNCATED AT 250 WORDS)

To explain tolerance of heat and cold in gerbils (Gerbillus campestris) in their natural environment, a comparative study was made of thermoregulatory reactions in these animals and white mice (Mus musculus) of the same body mass exposed for 2-3 h to ambient temperatures (Ta) ranging from -23 to 40 degrees C. Metabolic rate (MR), evaporative heat loss (EHL), colonic temperature (Tb), and electromyographic activity (EMG) were measured. Nonshivering thermogenesis (NST) was also evaluated from the increase in MR after norepinephrine injection. In gerbils, tolerance of cold was higher than in mice; there was no fall in Tb in cold-acclimated (CA) and control (TN) gerbils after 3 h of exposure at -20 and -10 degrees C Ta, respectively; peak MR (PMR) reached five to six times resting MR (RMR) in gerbils and four to five times in mice. In gerbils, RMR was 35% below that of mice. In TN gerbils, EHL did not increase before 38 degrees C Ta; EHL increased at 26 degrees C in mice. In both animals, cold acclimation increased cold tolerance, PMR, RMR, and NST. Low RMR, high Tb, and mainly burrowing habits preserve gerbils from overheating and save water in hot and arid environments, and a conspicuous tolerance of cold allows them to live and forage in the wild during the cold night.

The night monkey, a tropical monkey, is the only nocturnal simian; its thermoregulation was studied for comparison with other nocturnal or diurnal primates and other tropical mammals. Resting metabolic rate was 2.6 W (closed-circuit method) and 2.8 W (open-circuit method), 24 and 18% below the value predicted from body mass. The thermoneutral zone was very narrow; the lower critical temperature (LCT) was 28 degrees C and the upper critical temperature (UCT) was 30 degrees C. The body temperature (Tb) was at its minimum (38 degrees C) at an ambient temperature (Ta) of 25 degrees C, thus below the LCT. At low Ta, the increase in metabolic rate (MR) was smaller than predicted by the Scholander model, since MR intersected to a Ta 13 degrees C above Tb when extrapolated to MR = 0; this was attributed to a decrease of body surface area by behavior. The thermal conductance at the LCT was low: 2.3 W . m-2 . degrees C-1. Above the UCT, panting was the major avenue of heat loss. The response pattern of nocturnal habits, low resting metabolic rate, low thermal conductance, and panting in the night monkey, unique among simians, is found in many other mammals of tropical and hot desert habitats; it may be considered as an alternative adaptation to the thermal environment.

1. 1.|A high and constant temperature is an indispensable complement of tachymetabolism: it allows for energy expenditure while avoiding the risk of overheating. 2. 2.|There are no organs specifically responsible for thermoregulation although the different effectors are co-ordinated by the CNS to control body temperature. Homeothermy is partly determined by passive thermal equilibria, the organism sets a chosen regulated internal temperature, especially in the CNS, and, finally, adapts itself to varying conditions of environment and activity. 3. 3.|The multiplicity of organ systems called upon, and the relative autonomy of their control, allow the choice of those reactions least expensive and least involved in other functions.

The effect of catecholamines on oxygen uptake in dog hind limb skeletal muscle was continuously calculated from arterio-venous O2 saturation difference and blood flow data. Adrenalin and noradrenalin injected or perfused intraarterially or intravenously, always increased oxygen uptake to the same extent. The rise in consumption resulted mainly from an increase in the extraction of oxygen from blood under all hemodynamic conditions. Such an effect was repeatable by multiple short-spaced injections. The results suggest that adrenalin, as well as noradrenalin, actually increase oxygen consumption, independently of their vascular effects.

26 subjects were exposed either to constant temperature in a water bath or to different air temperatures. A differentiation was made between the comfort temperature and the conscious cutaneous thermal sensation.When thermal sensation of the hand was tested for different internal temperatures it was found that the same superficial (skin) temperature could be agreeable or disagreeable depending on the existing internal temperature. Those skin temperatures which lead to normalization of the internal temperature were agreeable; conversely those skin temperatures which increased deviation of the internal temperature from normal were disagreeable.In man there are two sensory components in thermal perception, one superficial discriminative, and one deep which permits appreciation of agreeable and disagreeable.

The capacity for nonshivering thermogenesis (NST) was examined in 26- to 27-day cold-acclimated (CA) muscovy ducklings reared for 21 days at 4 degrees C. Metabolic rate and integrated electromyographic (EMG) muscle activity were measured at ambient temperature ranging from -10 to 28 degrees C. Compared with controls reared at 30 degrees C, CA ducklings were more resistant to cold and had higher peak metabolic rate in extreme cold. Shivering threshold temperature of CA ducklings was 14.2 degrees C lower than lower critical temperature, whereas for controls the two temperatures were similar. Thus CA ducklings exhibited an NST in moderate cold. In addition, at temperatures that produced shivering, EMG activity in CA duckling muscle was lesser than that of controls, even at a higher metabolic rate. Because these ducklings are devoid of brown adipose tissue, these results indicated an increased thermogenic efficiency of muscular activity in CA ducklings.

Emperor penguins breed during the cold antarctic winter. The males incubate the single egg while fasting for up to 4 mo and losing some 20 kg of their body mass. Fasting captive birds under outdoor conditions lost from 0.145 to 0.434 kg day -1. Mean resting metabolic rate, 49.06 W for 24.8 kg body mass, is 7 and 27%, respectively, higher than predicted from general metabolic equations for birds. Minimal thermal conductance, 1.31 W m-2 degrees C-1, is within the range for other birds. The lower critical temperature is about -10 degrees C; this can be related to large body size (20-40 kg) and to body shape, giving a smaller relative surface area than for other birds. Rigidity of the feathers explains why winds of moderate speed (up to 5 m s-1) have little effect on heat loss. At very low temperatures the behavior of huddling close together is essential in reducing metabolic rate. Without this behavior, survival during the long fast (up to four mo) at winter temperatures would be impossible.