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1.
  • 1.1. The adult possums showed a circadian rhythm of body temperature with a peak in temperature around midnight and a nadir at noon.
  • 2.2. The young possum within the pouch displayed a circadian rhythm with the highest temperatures during the day and the lowest in the early evening.
  • 3.3. Although the body temperature of the young possum exceeded that of the mother occasionally, for the major part of the 24 hr the body temperature of the young was lower than that of the mother.
  • 4.4. The young possum could maintain a steady body temperature between 140 and 167 days post partum. A circadian rhythm of temperature was observed between 157–190 days post partum.
  • 5.5. All adipose tissue examined with the light and electron microscope had the morphology of white adipose tissue.
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2.
  • 1.1. In 43 European bison divided into three groups (Group A, 3–8-month-old calves; Group B, 18-month-7-year-old young bison; Group C, 12–24-year-old bison) the rectal, humerus region and abdomen region temperatures were measured.
  • 2.2. The experiments were carried out in winter months, from mid-December to mid-March.
  • 3.3. The mean rectal temperatures changed from 38.55°C in calves to 38.15°C in the oldest bison.
  • 4.4. The mean temperatures of the humerus region changed from 20.69°C in calves to 21.49°C in older bison.
  • 5.5. The mean temperatures of the abdomen region changed from 20.79°C in calves to 22.17°C in older bison (Gr. B).
  • 6.6. The cluster analysis divided the bison into four groups named hot, warm, cool and cold bison.
  • 7.7. Only air temperature measured 2 m above the ground and snow cover influenced the integrated bison temperature. Age, sex and mass as well as some environmental factors had no influence.
  • 8.8. Measurements made 1 to nearly 4hr after a bison's death showed a drop in rectal temperature and mostly increases in temperatures of the humerus and abdomen regions.
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3.
  • 1.1.|The activity pattern of 50 cold receptors of the rabbit nose back skin was investigated.
  • 2.2.|The latency of the response of individual cold receptors to identical cold stimuli varied between 0.8 ± 0.3 to 29.4 ± 4.5 s; maximal firing rates are attended after 5.5 ± 0.5 to 72.2 ± 6.2 s. Characteristic phasic responses are only demonstrated by short latency receptors.
  • 3.3.|The results suggest that cold receptors are distributed throughout the skin of the rabbit's nose.
  • 4.4.|Changes of temperature gradients between different skin layers were measured at different ambient temperatures.
  • 5.5.|It is suggested that cold receptors might indicate heat flow through the skin.
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4.
  • 1.1. The young of the bandicoot and possum are of similar weight at birth (200–250 mg) but by day 50 post-partum have weights of 100 and 20 g, respectively. The aim of this study was to determine whether the disparate growth rate was associated with a difference in the transfer of thyroxine from mother to young.
  • 2.2. Radioactive thyroxine was injected intramuscularly into the lactating female and 24 hr later a blood sample was obtained from the mother and the pouch young removed. The amount of radioactive thyroxine remaining in the blood and within the young was determined.
  • 3.3. The data obtained indicated that milk is a source of thyroid hormones in early pouch life.
  • 4.4. The hypothesis that greater quantities of thyroxine are transferred in the milk of bandicoots than that of brushtail possums is not supported.
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5.
  • 1.1. The mechanism of action of glyburide (a sulfonylurea) on muscle has been investigated by measuring glucose uptake and glucose transporter (GLUT4) protein levels after chronic glyburide treatment.
  • 2.2. A dietary induced insulin resistant rat model (4 wk of high-fat, high-sucrose feeding) was given glyburide (2mg/kg/day) for 10 days and glucose uptake was measured in a perfused hindquarter preparation.
  • 3.3. Protein levels of the GLUT4 glucose transporter were determined by Western analysis.
  • 4.4. After 7 days of treatment, rats fed glyburide had lower blood glucose concentrations 2 hr (72 ± 5 vs 103 ± 12 mg/dl) and 24 hr (97 ± 7 vs 123 ± 7 mg/dl) after glyburide administration with no difference in serum insulin levels compared to vehicle treated animals.
  • 5.5. Glucose uptake was approx doubled in basal state (0 insulin) in response to glyburide (2.8 + 0.4 vs 1.7 ± 0.2μ mol/g per hr).
  • 6.6. Maximal insulin (100 nM) stimulated glucose uptake tended to be higher in the glyburide treated group, but did not reach statistical significance (8.0 ± 0.7 vs 7.0 ± 0.6 μmol/g per hr).
  • 7.7. Western analysis revealed no significant effect of glyburide on the GLUT4 protein level in skeletal muscle.
  • 8.8. These results suggest that glyburide alters glucose uptake through some mechanism other than alterations in the level of the GLUT4 glucose transporter protein.
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6.
  • 1.1. When placed in a temperature gradient, 3–10 day old mice injected with living Escherichia coli or with E. coli endotoxin, select 2–3°C lower temperatures than their litter-mate controls injected with saline.
  • 2.2. At the lower selected temperature (32°C) young mouse pups resist bacterial infection for longer and tolerate higher doses of endotoxin than at the temperature selected by the controls (35°C).
  • 3.3. It is possible that a controlled hypothermic state, here called cryexia, is in small mammals an alternative strategy to fever for coping with infections.
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7.
  • 1.1. The adrenal cortex is necessary for survival of echidnas at low ambient temperatures. In this study, adrenal gland activity was investigated in echidnas exposed to 2 days of cold (14°C) and fasting, alternating with 2 days at room temperature and feeding ad lib.
  • 2.2. In the cold. 2.75 ± 0.29% (SD) of the initial body weight was lost daily. Plasma amino acid concentration did not change while glucose concentration decreased from 2.6 ± 0.3 to 1.5 ± 0.3 mmol/l with consecutive sessions of cold.
  • 3.Plasma concentrations of corticosterone (7.2 ± 1.4 nmol/l) and cortisol (4.4 ± 1.9 nmol/l) were unchanged by repeated cold exposure. However, the adrenal response to ACTH stimulation decreased and the clearance of corticosteroids increased after cold exposure.
  • 4.It was concluded that exposure to cold increases the utilization of glucocorticoids and decreases the capacity for their biosynthesis.
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8.
  • 1.1.|Vaginal temperatures of 15 Bos taurus cattle were monitored for 17 days in daily pens exposed to normal environmental fluctuations.
  • 2.2.|Regressions of vaginal temperature on ambient temperature were made for each collection time in the 24 h cycle. Slopes of regressions provided an index of animal sensitivity to environmental temperature.
  • 3.3.|Fluctuations in sensitivity occurred throughout the day with positive slopes excepts at 0630 h.
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9.
  • 1.1. Osmotic measurements were made on the perivisceral coelomic and water vascular fluids of 4 species of northwest Pacific starfish and their stable sea-water media.
  • 2.2. Mean levels of both fluids were hyperosmotic in every species, often at statistically significant levels.
  • 3.3. For all species combined, mean hyperosmolality (mosmol/kg ± SE) of perivisceral coelomic fluid was 1.49 ± 0.17, and water vascular fluid 6.07 ± 0.74.
  • 4.4. The hyperosmotic nature of these fluids contributes to water balance, working in conjunction with madreporitic inflow and other factors.
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10.
  • 1.1. A method is described for the accurate and rapid measurement of protein- and non-protein-bound cortisol by miniature gel filtration in small volumes of plasma, e.g. of rodents.
  • 2.2. Binding of cortisol by guinea pig plasma proteins is strongly reduced at elevated temperature (4°C: 102 ± 12ng/ml; 40°C: 5 ± 2 ng/ml).
  • 3.3. Incubation of guinea pig plasma with 1–5000 ng cortisol resulted in a dose-dependent increase in cortisol bound to proteins (specific binding by corticosteroid binding globulin: 230 ± 12 ng/ml).
  • 4.4. Administration of 20 IU (1–24)ACTH induced a significant increase of total protein-bound and non-protein-bound cortisol.
  • 5.5. Values reported in this study agree well with those of previous investigations, in which bound and non-bound glucocorticosteroids were separated by gel filtration on large Sephadex® columns.
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11.
  • 1.1. Tyrosyl protein sulfotransferase (TPS) activity in the newborn and mature rat brain was studied using the cholecystokinin derivative terbutyloxycarbonyl-Asp-Tyr-Met-Gly-Trp-Met-Asp-PheNH2, BocCCK-8(ns), as the peptide substrate.
  • 2.2. TPS activity was enriched 4 times in the microsomal and synaptic vesicular enriched fractions of rat cerebral cortex.
  • 3.3. CCK-8 content, in the subcellular fractions and the peptide sulfation activity distribution was in accord with the hypothesis that tyrosyl protein sulfotransferase plays a key role in the maturation process of bioactive CCK.
  • 4.4. TPS activity measured in membranes from newborn brain was 2.5 times higher than the activity observed in the mature brain membranes with a Vmax = 0.83 ± 0.05 and 0.31 ± 0.02 respectively. The apparent KM for the sulfate donor, 3'-phosphoadenosine 5'-phosphosulfate (PAPS), was similar, 94 ± 4 nM and 90 ± 6 nM and the kM for the peptide substrate, BocCCK-8(ns), was 234 ± 16 μM and 160 ± 12 μM in the newborn and adult brain membranes respectively.
  • 5.5. TPS activity reached normal mature values within 20 days of age.
  • 6.6. These data support the idea that tyrosyl protein sulfation is an important process in the secretion mechanism and in the CCK maturation.
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12.
  • 1.1. Adenosine 5'-phosphoramidate hydrolase of 29 kDa was isolated from rat liver cytosol.
  • 2.2. It consisted of two subunits of 14 kDa.
  • 3.3. It hydrolyzed nucleoside 5'-monophosphoramidates into nucleoside 5'-monophosphates and ammonia, while it did not hydrolyze adenylyl phosphoramidate, adenylyl imidodiphosphate and N-phosphorylated compounds like phosphocreatine, Nω-phosphoarginine, 6-phospholysine and 3-phosphohistidine.
  • 4.4. Divalent cations and cyclic AMP had no effect on the hydrolytic activity.
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13.
  • 1.1. Sulphate labelled proteoglycans (PG) synthesized by cultured human arterial smooth muscle cell have been quantified using an improved method based on a combination of specific enzymes and ethanol precipitation.
  • 2.2. The present method gives quantitative data of PGs and subclasses allowing batchwise analysis of a large number of samples.
  • 3.3. Approximately 81 % ± 1.7% (mean ± SD, n = 6) of total PGs synthesized by human arterial smooth muscle cells accumulated in medium.
  • 4.4. In cell layer and medium chondroitin sulphate proteoglycan constituted 65.0% ± 0.3% and 75.8% ± 0.7% (mean ± SD, n = 3), respectively of sulphated PGs.
  • 5.5. Heparan sulphate proteoglycan accounted for 26.8% ± 0.6% in cell layer and 22.6% ± 0.5% (mean ± SD, n = 3) in medium of sulphated PGs.
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14.
  • 1.1. The optimum pH for measurement of aspartate transcarbamylase activity in oyster tissue was determined to be 9.35 while the optimum temperature was 39.5°C.
  • 2.2. Aspartate transcarbamylase activity varied significantly over short periods of time (hr) possibly due to fluctuations in the amount of food digested.
  • 3.3. The composition of the oyster's diet also affected the levels of aspartate transcarbamylase activity in oyster tissues.
  • 4.4. Those oysters fed an egg yolk-starch diet contained significantly lower aspartate transcarbamylase activity than oysters fed an egg yolk-starch-salmon oil diet or a casein-starch-salmon oil diet.
  • 5.5. The aspartate transcarbamylase activities in oysters fed Phacedactylum tricornutum or a starch diet were not significantly different from the activities in oysters fed the egg yolk-starch diet.
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15.
  • 1.1. Glucose pool size, space, entry rate, and turnover time were estimated from the specific radioactivity vs time curves of [3H] and [14C]glucose administered as a single injection in the euro (Macropus robustus erubescens) and the sympatric feral goat (Capra hircus).
  • 2.2. Digestible energy intake was greater (P < 0.05 ± SE) in the goat than in the euro (798 ± 64 vs 624 ± 31kJ/kg0.75 × day).
  • 3.3. However, there were no significant differences between the two species in parameters of glucose metabolism.
  • 4.4. The use of an implantable osmotic infusion pump to deliver isotopic glucose showed promise as a means of avoiding the stress involved with the single injection technique.
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16.
  • 1.1. Short-chain fatty acid absorption in hen colon is protonated across the apical border coupled to an apical electrogenic proton pump.
  • 2.2. The surface pH of the isolated colonic epithelium was 6.27 ± 0.05, when incubated in Krebs-phosphate buffer pH 7.0.
  • 3.3. Propionate 7 and 40mmol/l in the incubation medium (pH 7.0) increased microclimate pH to 6.47 ± 0.04 and 6.56 ± 0.04. Inhibition of metabolic activity by potassium cyanide 1 mmol/1 increased surface pH to 6.66 ± 0.06.
  • 4.4. The calculated concentration of propionic acid in the microclimate is near-linearly related to the propionate concentration. Thus, the acid microclimate is not responsible for the Michaelis-Menten like kinetics of propionate transport.
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17.
  • 1.1. Nitrogenous excretion in the form of ammonia was determined in common carp of 65.0 ± 8.0 g body weight in metabolism chambers. The fish were fed with 20, 35 and 50% dietary protein at 1, 2 and 3% body weight per day ration level.
  • 2.2. Nitrogenous excretion as a percentage of ingested food increased with an increase of dietary protein but decreased with an increase of ration level.
  • 3.3. The energy lost in excretion ranged from 4.19% with 20% dietary protein at 3% ration level to 8.74% with 50% dietary at 1% ration level.
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18.
  • 1.1. The entire oxygen dissociation curve (ODC) and the effects of temperature, pH and 2,3-diphosphoglycerate (DPG) on this curve, have been compared in four mammalians: man, dog, horse and cattle.
  • 2.2. If the oxyphoric capacities are similar between these species (around 1.39ml O2/gHb), their P50, measured in standard conditions, i.e. at pH 7.4;.pCO2 40mmHg and T 37°C, varies between 23.8 (± 0.8) mmHg for the horse, 25.0 (± 1.4) mmHg for cattle, 26.6 (± 1.2) for man and 28.8 (± 2.6) mmHg for the dog.
  • 3.3. The higher dispersion of the dog's P50 is due to difference between breeds; in seven breeds investigated, the P50 ranges from 25.8 (spaniel) to 35.8 (hound).
  • 4.4. We noted no sex difference in the four species.
  • 5.5. The DPG level is confirmed to be low in cattle (< 1 μmol/gHb) as compared to man (13.5 ± 2.1 gmmol/gHb), horse (16.9 ± 1.1 gmmol/gHb) and dog (19.4 ± 2.8 μmol/gHb).
  • 6.6. The oxygen exchange fraction defined as the difference in vol% between a pO2 of 80 and 35 mmHg is, respectively, 3.6 (± 0.6) vol% for cattle, 4.0 (0.4) vol% for the horse, 5.5 (± 0.5) vol% for man and 6.6 (± 1.7) vol% for the dog.
  • 7.7. The position and shape of the ODC, as well as T, DPG and pH effects, indicate that the haemoglobin of man and dog seem better adapted to O2 delivery as compared to the horse and cattle.
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19.
  • 1.1. Experimental evidence is presented that short-term thermoregulatory adjustments occurring not far from thermoneutrality, involve temperature changes that are opposite in sign in different body regions. In man, exposure to hot ambient temperature (Ta), induced a decrease in esophageal and rectal temperatures. In rabbit, exposure to cold Ta induced an increase in hypothalamic temperature.
  • 2.2.|Similar results could be obtained by simulation on a mathematical model of man's thermoregulatory system.
  • 3.3.|The above results, as well as analogues results described in the literature, can be accounted for by a scheme of interpretation standing on current concepts of thermoregulation. If the gain of the thermoregulatory system is high, thermal stimulation of a region of the body will induce opposite temperature changes in other regions of the body.
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20.
  • 1.1. The level of carbonic anhydrase activity in the red cells was measured in sheep fetuses at different times after conception: 39, 56, 77, 90 and 140 days, the last being close to full term. Measurements were also made on blood from four of the mothers.
  • 2.2. There was a low level of the enzyme present in the 39 day fetuses (0.037 enzyme units (E.U.)/100 μg Hb) and its increase up to 90 days of gestation (0.19 E.U./100 μg Hb) had a form approximating exponential.
  • 3.3. The earliest levels were only 11% of the full term levels and only 4% of the adult levels previously reported.
  • 4.4. Even the earliest samples were of blood that was fetal rather than embryonic but these results are the earliest carbonic anhydrase activities reported in this mammal.
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