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1.
  • 1.1. The role ofinterleukin-1 (IL-1) in sepsis-induced muscle proteolysis was assessed by treating septic rats with recombinant IL-1 receptor antagonist (rIL-Ira).
  • 2.2. In initial experiments, we tested the effectiveness of IL-Ira in preventing muscle proteolysis induced by administration of IL-1.
  • 3.3. When normal rats were treated with rIL-α (three intraperitoneal doses of 100 μ g/kg body weight each over 16 hr), total and myofibrillar muscle protein breakdown rates, measured as release oftyrosine and 3-methylhistidine, respectively, by incubated extensor digitorum longus muscles, were significantly increased.
  • 4.4. This metabolic response to IL-α was completely abolished by rIL-Ira, administered as three intraperitoneal doses of 3 mg/kg body weight each over 16hr.
  • 5.5. In subsequent experiments, sepsis was induced in rats by cecal ligation and puncture (CLP); non-septic rats were sham-operated.
  • 6.6. Treatment of septic rats over 16hr with a total dose of 25mg/kg body weight of rIL-Ira reduced, but did not normalize, the increased muscle protein breakdown rates seen during sepsis.
  • 7.7. When the dose of rIL-Ira was more than doubled and given as a constant infusion at a rate of 4.2 mg/kg body weight/hr for 16 hr, the increased rate of muscle proteolysis in septic rats was normalized.
  • 8.8. The present study offers the first direct evidence that IL-1 is involved in the regulation of muscle proteolysis during sepsis.
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2.
  • 1.1. The hepatic d-aspartate oxidase activity was found to be higher in female ddY and ICR mice than in their male counterparts. On the contrary, the free d-aspartate content in the liver was lower in female mice than in male mice, suggesting that d-aspartate is actually metabolized by d-aspartate oxidase in vivo.
  • 2.2. Oral administration of d-aspartate to the animals increased the hepatic d-aspartate oxidase activity 2–3 fold in both genders without any significant difference in the rate of the increase between the genders.
  • 3.3. Several peroxisomal enzyme activities other than d-aspartate oxidase examined were not affected by this treatment.
  • 4.4. Experiments in vitro suggested that the increase in the d-aspartate activity might be explained in part by stabilization of the enzyme by d-aspartate.
  • 5.5. The administration of clofibrate, a peroxisome proliferator, to male mice, increased the hepatic d-aspartate oxidase activity with a significant simultaneous decrease of d-aspartate content in the liver, in agreement with a possible role of the enzyme n vivo.
  • 6.6. On the other hand, the administration of clofibrate or dehydroepiandrosterone to female mice decreased the d-aspartate oxidase activity.
  • 7.7. The peroxisome proliferators were suggested to act to eliminate the gender difference of hepatic d-aspartate oxidase activity in mice.
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3.
  • 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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4.
  • 1.1. Rates of water loss in Megetra cancellata were very high compared to those reported for other xeric arthropods.
  • 2.2. Hemolymph weight in hydrated animals was 43.0% of the total body weight while it was 24.7% in desiccated animals that had lost 16.1% of their body weight as water.
  • 3.3. Hemolymph osmotic potential increased from 417 to 447 mOsm/kg in desiccated beetles, but osmotic regulation was evident.
  • 4.4. Total hemolymph protein mass and concentration decreased in desiccated beetles while amino acid concentrations remained constant (at about 70 mM).
  • 5.5. Na+ and −PO4 concentrations increased in desiccated beetles.
  • 6.6. Cl and K+ concentrations in desiccated beetles were equal to those in undesiccated beetles.
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5.
  • 1.1. In relation to body weight changes resulting from evaporative water losses of up to 37% of initial body weight:
    • 1.1.(a) Plasma chloride and potassium concentrations increased in proportion to total body water losses.
    • 1.2.(b) Plasma urea concentrations increased at greater rates than expected from the sum of basal synthesis and dehydration.
    • 1.3.(c) Plasma sodium concentrations initially increased less rapidly than expected from total body water losses, but by losses of 30% of initial body weight closely approximated predicted concentrations.
    • 1.4.(d) Plasma volumes decreased slightly faster than expected, while hematocrits increased as expected.
  • 2.2. Skeletal muscles and the ventricular muscles of the heart retained water to greater degrees than expected. Dehydration did not elicit net shifts in Na+ K+, Cl or amino acids between the intracellular and extracellular compartments in either skeletal muscle or ventricle.
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6.
  • 1.1. The weight and energy content of sloughed skins of 92 individual snakes of 22 different species in three families were measured.
  • 2.2. Weight and total energy content of shed skins were highly correlated with body weight.
  • 3.3. The heat of combustion (kJ/g) of sloughed skins varied significantly among families and was higher in species having unkeeled scales than in those with keeled scales.
  • 4.4. The presence of keels significantly affected weight of skins, even when skin weight is adjusted for covariance with body weight.
  • 5.5. Neither body weight nor ambient temperature significantly affected the heat of combustion of sloughed skins.
  • 6.6. The energy content of shed skin, expressed as a proportion of daily metabolism, decreased with ambient temperature, but the effect is minimized in large snakes.
  • 7.7. Small snakes expended relatively less energy in sloughed skins than large snakes when the expenditure is expressed in terms of total daily metabolized energy.
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7.
  • 1.1. The feeding of 0.5% (3,5,5-trimethylhexanoyl)ferrocene (TMH-ferrocene) in rats resulted in a severe and progressive liver siderosis (total liver iron, 30 mg/g liver wet weight, after 30 weeks).
  • 2.2. High concentrations of an iron-rich ferritin (up to 250 mg/l) were detected in serum of heavily iron-loaded rats forming a large fraction of non-transferrin-bound-iron (5000 μg/dl in maximum).
  • 3.3. Ferritin and not haemosiderin was the major iron storage protein in the liver.
  • 4.4. The total liver iron concentration (from 0.4 to > 30 mg Fe/g wet wt) but not the cytosolic low-molecular-weight-iron fraction (from 0.5 to 2.5 μM) was extremely increased during iron-loading.
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8.
  • 1.1. Laboratory mice were bred in groups of 20, 60 and 100 mice per cage. Male to female ratio was 1:1.
  • 2.2. The experiment was carried out in autumn-winter and winter-spring.
  • 3.3. Levels of ascorbic acid were determinated in homogenates of adrenal glands after 10 weeks of breeding.
  • 4.4. Three- and five-fold increase of number of mice in the same area caused the decrease of ascorbic acid level in adrenal glands of active males, non-pregnant and nursing females. In pregnant females this correlation was not observed.
  • 5.5. Decrease of ascorbic acid level due to increase of adrenal glands' weight was also observed.
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9.
  • 1.1. Ration and body size effects on specific dynamic action (SDA) were investigated in the supralittoral isopod Ligia pallasii using seaweed and chemical diets.
  • 2.2. SDA increased asymptotically with ingested meal size for all diets.
  • 3.3. Body weight had a significant positive effect on SDA for only one of the six diets tested, but weak tendencies were present in the data for the other diets.
  • 4.4. SDA appeared to increase geometrically with increasing concentration of amino acids at high ration levels.
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10.
  • 1.1. Growing male kittens were fed an 18% casein diet supplemented with 2, 3, or 4% l-methionine (MET) for 6 weeks.
  • 2.2. Free MET concentration in liver increased 30-fold and cystathionine two- to three-fold; the activity of adenosyl-MET transferase and cystathionase also increased but remained lower than previously found in rats.
  • 3.3. Taurine concentration in liver decreased in cats fed excess MET and appeared to depend on taurine intake.
  • 4.4. Alanine aminotransferase activity was high in all groups while serine dehydratase activity was very low.
  • 5.5. Pyruvate kinase and malic enzyme activities which are normally low in cat liver increased after excess MET. Also, glucose 6-phosphate and 6-phosphogluconate dehydrogenases increased.
  • 6.6. Cat liver metabolism showed limited adaptation to an excess dietary intake of methionine compared to that found in rats.
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11.
  • 1.1. The effect of thermal acclimation on the activity of liver enzymes of B. pholis and on the ultrastructure of the liver was studied.
  • 2.2. Significant increases in the activities of SDH and G6PDH, but not of LDH were found after cold-acclimation.
  • 3.3. E.M. measurements suggested that cold-acclimation resulted in an increase in the size of liver cells and their nuclei, and in the number, but not the size of liver mitochondria.
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12.
  • 1.1. Measurements of the rate of nitrogen consumption, total nitrogen and ammonia excretion and nitrogen absorption of bream, Abramis brama L. (body weight range 0.4–519 g wet wt) were made at 10, 15 and 20 C.
  • 2.2. Fish were fed once daily on live zooplankton collected in Lake Balaton and cultured Tubifex sp. at 5–15% of their body weight.
  • 3.3. Fish size and temperature had a combined effect on the rate of total nitrogen excretion. Total nitrogen excretion did not increase proportionally with an increase in consumption.
  • 4.4. On average, 52–80% of the nitrogen consumed with food was excreted by bream.
  • 5.5. The greatest part of total nitrogen excretion was ammonia and its proportion in the total ranged between 53 and 75%.
  • 6.6. Temperature did not have any significant effect on the proportion of excreted ammonia and the rate of excreted total nitrogen was the only factor determining its proportion in the total.
  • 7.7. The rate of nitrogen absorption of bream was surprisingly very high.
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13.
  • 1.1. Developing eggs of whitefish (Coregonus lavaretus L.) and vendace (Coregonus albula L.) were kept at 1–2°C and some eggs taken gradually up to 8°C to provoke mass hatching of embryos.
  • 2.2. Wet weight, dry matter and the contents of lipid, protein and ash were measured in fish during the course of experiment.
  • 3.3. Dry matter content decreased gradually in whitefish eggs from 15.64 to 11.95% during 1 month at 1–2°C, whereas vendace eggs showed only a slight decrease from 16.27 to 15.53%.
  • 4.4. In both species protein content decreased but lipid increased when approaching the natural time of hatching.
  • 5.5. During delayed hatching at low water temperatures protein contributes to catabolism, whereas lipid content decreased only in the later phase of the experiment.
  • 6.6. Larvae starved for 10 days after hatching lost increasing amounts of dry matter (from 26.1 to 50.3% of body weight) and protein (from 18.7 to 45.9% of body weight) as they remained longer in cold water as embryos.
  • 7.7. A correspondence was found between assessment of metabolic utilization of body stores based on chemical analysis of fish body and previous work on oxygen consumption and nitrogen excretion.
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14.
  • 1.1. The glycogen content of the mantle tissue reached a maximum in the summer (May–July) with levels of 41.0–53.5% of the dry tissue weight.
  • 2.2. Seasonal changes in glycogen synthetase activity showed that the I-activity (independent of G6P) increased up to 10-fold in June as compared with December. The measured I-activity of glycogen synthetase was sufficient to account for the accumulation of mantle glycogen in the summer.
  • 3.3. The I-activity of glycogen synthetase declined rapidly in July of each year. A possible role for the inhibition of glycogen synthetase by high levels of tissue glycogen is suggested.
  • 4.4. The I-activity in the mantle tissue of mussels on the shore was higher than that for animals starved in the laboratory for 2–3 days. The differences were minimal in early May but increased markedly in late May–July. Starved mussels returned to the shore showed an increase in I-activity of glycogen synthetase.
  • 5.5. Injection of 30 μmol glucose into the adductor muscle increased the concentration of glucose in the mantle fluid to 2.0–2.5 mM. A similar injection of 60 μ mol glucose resulted in a time-dependent increase in the I-activity of glycogen synthetase.
  • 6.6. Injection of mussels with mammalian insulin or anti-insulin serum had no effect on the activity of glycogen synthetase. Our results are at variance with those of other workers who have used the mammalian hormone in molluscan studies (see Discussion).
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15.
  • 1.1. Seasonal acclimatization effects on oxygen consumption, body temperature, and body weight were evaluated in three different experimental groups of Dipodomys panamintinus.
  • 2.2. Body weights of wild field as well as captive animals housed in outdoor sand cages were maximum in winter and lowest in summer for both sexes.
  • 3.3. Mean oxygen consumption was maximum in winter and lowest during spring in both sexes of the wild field and captive exposed groups.
  • 4.4. Neither weight nor oxygen consumption of indoor control animals varied with the seasons.
  • 5.5. No significant differences in body temperatures were observed during either the fall or winter seasons.
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16.
  • 1.1. The s.c. administration of cortisol to hamsters (50 mg/kg body wt/day for 4 days) produces a significant increase in maltase sucrase, alkaline phosphatase and leucineaminopeptidase activity in intestinal mucosa.
  • 2.2. Lactase activity is unaffected by cortisol.
  • 3.3. Gamma-glutamyltranspeptidase activity increases slightly in females but remains unchanged in males.
  • 4.4. Cortisol causes increase in proline and glycine absorption without changing the absorption of lysine.
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17.
  • 1.1. Starving Notothenia coriiceps nn/lecta at 1°C for 20 days resulted in a loss of 4.22 gcal/kcal per day.
  • 2.2. During starvation energy was obtained from lipid and carbohydrate stores of the liver and red muscle.
  • 3.3. Feeding N. coriiceps neglecta low lipid, high protein shrimp meat at 18.9 gcal/kcal per day at 1°C for 20 days resulted in a gain of 8.5 gcal/kcal per day.
  • 4.4. The level of carbohydrate in the liver and red muscle increased five times.
  • 5.5. Gross growth efficiency (K1) equalled 0.52.
  • 6.6. Net growth efficiency (K2) equalled 0.67.
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18.
  • 1.1. Seasonal variation in total lipids was examined in several body components of the turtle Sternotherus odoratus.
  • 2.2. Carcass fat stores in both sexes were depleted during winter. Additionally, a decline in carcass lipids was associated with increases in gonadal mass.
  • 3.3. Concentrations of liver lipids were maximal during August and minimal during winter.
  • 4.4. Males showed little seasonal change in plasma lipid levels, whereas females had seasonal peaks temporally associated with ovarian development and carcass fat storage.
  • 5.5. Ovarian concentrations of lipids were minimal after nesting and increased during fall.
  • 6.6. Results suggest that S. odoratus uses stored fats both for reproduction and maintenance during winter.
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19.
  • 1.1. Fetal lung metabolic response to maternal fasting late in gestation was investigated.
  • 2.2. Maternal fasting 4 days before term was associated with low fetal plasma glucose and insulin levels but increased levels of fetal plasma glucagon, glycerol, lactate and fatty acids.
  • 3.3. Fetuses from fasted mothers showed a significant decrease in body weight (30%), lung weight (30%) and lung glycogen (46%), but no change in lung protein, phospholipid or total lung DNA, suggesting that lung size is affected more than maturation.
  • 4.4. Fetal lung slices incubated in vitro showed that lactate oxidation to CO2 equalled that of glucose in control fetal lungs and was unaffected by maternal fasting, while glucose oxidation was depressed (23%).
  • 5.5. Maternal fasting significantly decreased in vitro incorporation of [U-14C]-glucose, [U-14C]lactate and [1-14C]palmitate into lung phospholipids.
  • 6.6. Fetal lungs from fasted mothers showed increased conversion of lactate to glucose, indicating gluconeogenic potential by fetal lung.
  • 7.7. These studies show that plasma lactate serves as an important energy fuel and substrate for lipid synthesis for the fetal lung, and maternal fasting markedly alters fetal lung metabolism.
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20.
  • 1.1. Vitamin D3 (10IU and 100IU/100 g body weight) and 1,25(OH)2D3 (0.5, 5 and 50 U) were administered daily to unfed male carp Cyprinus carpio for 10 days. The serum calcium and inorganic phosphate levels were measured colorimetrically.
  • 2.2. The serum calcium level increased significantly in all treated groups; this increase is dose-dependent.
  • 3.3. The serum inorganic phosphate was elevated in the treated groups on days 3 and 5.
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