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1.
  • 1.1. Fatty acid and lipid class composition were determined in larvae of four marine species: Atlantic halibut (Hippoglossus hippoglossus L.), plaice (Pleuronectes platessa), cod (Gadus morhua) and turbot (Scophthalmus maximus) at hatching and prior to first feeding.
  • 2.2. Total fatty acid content decreased in the four species with up to 50% reduction in one of the halibut groups. Docosahexanaoic acid (22:6 n-3) was especially utilized.
  • 3.3. Low lipid utilization was found in turbot in relation to the other three species.
  • 4.4. Water environmental temperature may explain some of the differences in the fatty acid utilization and the source of metabolic energy between cold water species (halibut, cod, and plaice) and temperate species (turbot), in the period from hatching to prior to first feeding.
  • 5.5. Relative amounts of neutral lipids and phospholipids were similar in plaice, cod and halibut, approximately 25% and 75% of total lipids, respectively, and were approximately constant during the yolk-sac stage. Neutral lipids were dominant for turbot at hatching, accounting for 53–55% of the total lipids, while phospholipids predominated prior to first feeding, being 56–59%.
  • 6.6. Phosphatidylcholine was catabolized in halibut, plaice and cod but not in turbot, while phosphatidylethanolamine tended to be synthesized in all four species.
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2.
  • 1.1. Since glucose is one of the main energetic substrates for general metabolic processes in crustaceans, analysis of carbohydrate levels can furnish information on the energy metabolism of intact animals during osmoregulation.
  • 2.2. Different groups of Chasmagnathus granulata were transferred to different salinities (0 and 40%), and the glucose and glycogen concentrations in blood, gills, muscle and hepatopancreas were determined at the beginning of the experiment and 24, 72, 168 and 360 hr after the salinity changes.
  • 3.3. Differences in tissues carbohydrate levels were observed between summer and winter, that reflected differences in reserve mobilization.
  • 4.4. In the summer, hypo- and hyperosmotic shocks induced an increase in carbohydrate levels in almost all tissues studied, indicating gluconeogenesis.
  • 5.5. In the winter, a carbohydrate mobilization occurred only in the gills and hepatopancreas after both osmotic shocks.
  • 6.6. Thus, the substrate reserve used for energy production required for osmoregulation seems to be dependent on the season and tissues.
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3.
  • 1.1. A highly efficient cellulose digestion could be demonstrated in a primitive insect species, Thermobia domestica (Thysanura:Lepismatidae), by the application of a uniformly 14C-labelled substrate.
  • 2.2. Gut extracts exhibit distinct hydrolytic activities toward different cellulosic substrates (cellobiose, sodium carboxymethylcellulose and microcrystalline cellulose). Therefore, the complete cellular complex must be present.
  • 3.3. Besides cellulases, several other carbohydrates occur in the digestive juice, thus reflecting the omnivorous feeding habits of the insect.
  • 4.4. The crop was found to be the main site of carbohydrate digestiopn, also including cellulolysis.
  • 5.5. It is very likely that the cellulolytic enzymes derive from the gut tissues of the firebrat.
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4.
  • 1.1. The effects of seasonal variation on the carbohydrate and lipid metabolism of the Chasmagnathus granulata were investigated.
  • 2.2. Glycemia is high in winter and summer and low in spring and fall.
  • 3.3. The glycogen content in the hepatopancreas and muscle is higher in fall and winter, and decreases during spring and summer.
  • 4.4. The muscle lipids are higher in summer, and decrease during fall and winter whereas hepatopancreas lipids are higher except in the fall.
  • 5.5. The crabs show change in the metabolic pattern of lipids and carbohydrates during the seasons of the year.
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5.
  • 1.1. The physiology of the Djungarian hamster is described with special regard to breeding and development.
  • 2.2. The metabolic abnormalities are studied with special regard to carbohydrate and lipid metabolism.
  • 3.3. The data reveal this animal to exhibit a genetically determined inappropriate hyperglycaemia and to differ from all other species so far known by an early onset of urinary ketone body excretion.
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6.
  • 1.1. The collagen content in the abdominal muscle of seven species including shrimp, prawn, lobster and squilla varied among the species ranging from 1.1 to 6.2% of total tissue protein and the content in pereiopod and thoracic muscles of four species of crab varied ranging from 0.2 to 0.8%.
  • 2.2. These results indicate that the musculature in flexible part comprises a high proportion of collagen.
  • 3.3. The major collagen from the crustacean muscle was found to be similar to Type V collagen from the vertebrate muscle with respect to the solubility and amino acid composition.
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7.
  • 1.1. A study was carried out of post-natal evolution of the oxidative, glycolytic and contractile capacities in various types of rabbit muscle.
  • 2.2. At birth, muscles are non-differentiated and present very limited metabolic and contractile activity, metabolism is mainly oxidative in all muscles.
  • 3.3. Although muscular discrimination is manifest from the sixth week after birth, the glycolytic metabolism reaches its maximum capacity only after six to eight weeks.
  • 4.4. Subsequently, oxidative metabolic capacity steadily decreases until adulthood.
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8.
  • 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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9.
  • 1.1. The influences of age (5, 13 and 25-month-old rats), overload as obtained by denervation of synergists, and training on the metabolic capacity, relative muscle cross-sectional area occupied by each fibre type, capillarization and fatigue resistance of the rat m. plantaris were investigated.
  • 2.2. Creatine kinase, phosphorylase and citrate synthase activities were lower in muscles of 25 than in those of 13-month-old rats (P < 0.001).
  • 3.3. Overload resulted in an increased relative area of type I and II a fibres at all ages (P = 0.001).
  • 4.4. Capillary density decreased with overload and increasing age (P < 0.001).
  • 5.5. Fatigue resistance was higher in muscles of 13 than in those of 5-month-old rats (P < 0.05), and increased with overload (P < 0.05) at all ages.
  • 6.6. Fatigue resistance of the whole muscle was not closely related to its oxidative capacity in contrast to what is generally found for single fibres or motor units.
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10.
  • 1.1. A choriolytic enzyme was isolated from the hatching medium of the pike, Esox lucius.
  • 2.2. The enzyme is defined as hatching enzyme.
  • 3.3. The molecular weight of the enzyme is 24,000.
  • 4.4. The enzyme is a glycoprotein containing 2% carbohydrate.
  • 5.5. Its isoelectric point is 6.5.
  • 6.6. The pH optimum is around pH 8.
  • 7.7. The enzyme molecule contains two disulfide bonds but no free cysteine.
  • 8.8. Inhibitor studies and metal analysis show that the enzyme is a zinc-metalloprotease.
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11.
  • 1.1. Changes in metabolic rates and behavior were observed in tufted titmice (Parus bicolor) and Carolina chickadees (Parus carolinensis) exposed to varying conditions of artificial solar radiation, wind, and temperature in a wind tunnel experiment.
  • 2.2. During the wind-on condition, both species showed a significant decrease in mean metabolic rates in the high radiation treatments when compared to the low radiation treatments (P < 0.05).
  • 3.3. Titmouse orientation, posture and level of activity were significantly affected by radiation and wind conditions.
  • 4.4. Metabolic rates observed in the wind tunnel treatments without wind and at low radiation did not significantly differ from similar standard metabolic (black box) treatments (P > 0.05).
  • 5.5. Activity levels did not appear to directly affect metabolic rates observed in the wind tunnel treatments.
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12.
  • 1.1. Various blood parameters were monitored in resting and flown homing pigeons. A homing flight of 48 km lasting 60–80 min did not significantly alter plasma levels of total protein, electrolytes and plasma osmolality, which indicated maintenance of the homeostatic stability of the internal milieu during moderate exercise.
  • 2.2. Plasma concentrations of marker enzymes such as alanine aminotransferase (ALAT), aspartate aminotransferase (ASAT), laetate dehydrogenase (LDH) and creatine phosphokinase (CPK) that tend to denote muscle damage and metabolic flux in prolonged exercise, were also not altered, thereby indicating the steady state of tissue structure and function during a flight of this magnitude.
  • 3.3. Significant increases in plasma levels of uric acid and creatinine and decreases in plasma albumin were observed in the flown pigeons.
  • 4.4. The flight-induced increase in blood uric acid could be attributed to increased purine catabolism and the increase in creatinine to increased nucleotide turnover.
  • 5.5. It is suggested that the higher uric acid levels should not only enhance water conservation, but may also reduce flight-induced hyperthermia besides acting as an antioxidant defence against oxidative tissue injury.
  • 6.6. The rise in creatinine is indicative of the breakdown of phosphocreatine for energy during the initial period of flight prior to the utilization of carbohydrate and lipid as fuels.
  • 7.7. The decrease in plasma albumin should account for the albumin as lipid carrier lost in transport to the muscles during flight.
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13.
  • 1.1. The organic composition of the body tissues of eight species of deep-sea aspidochirotid holothurian, collected between 500 and 4100m depth in the NE Atlantic Ocean, was obtained by the biochemical analysis of protein, lipid, carbohydrate and % ash.
  • 2.2. The major organic class was protein with soluble lipid the major soluble fraction in the ovary. Carbohydrate values were consistently low.
  • 3.3. The calorific value was significantly higher in the ovary than in the other tissues.
  • 4.4. The total body calorific content for two selected species, Benthothuria funebris and Mesothuria lactea, was 25.62 and 26.24J/mg ash-free dry weight (AFDW).
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14.
  • 1.1. Results of investigations on direct calorimetry and simultaneous measurements of oxygen consumption and carbon dioxide and ammonia production of fish are summarized.
  • 2.2. By means of indirect calorimetric formulae, the heat production and the protein, carbohydrate and fat oxidation are calculated from the oxygen consumption and carbon dioxide and ammonia production.
  • 3.3. The lowest heat production values are obtained by long-term monitoring of groups of fish during darkness and under fasting conditions.
  • 4.4. It is concluded that the heat production of standard metabolism at 20°C is 700J/hr/MW (MW = metabolic weight, kg0.85).
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15.
  • 1.1. The major excreted acidic end products of the anaerobic and aerobic carbohydrate metabolism of Trichomonas vaginalis (ATCC 30001) were acetate and lactate. Glycerol-1-phosphate, pyruvate, malate and ethanol were also detected in the incubation medium, but they represented less than 3% of the total carbon excreted. Succinate could not be found. Under anaerobic conditions H2 and CO2 were produced. Under aerobic conditions O2 was consumed and CO2 produced.
  • 2.2. In the absence of exogeneous carbohydrate more acetate than lactate was produced. Glucose (50 mM) significantly increased acid production with lactate becoming the predominant product. Glucose also increased the anaerobic and aerobic gas exchange.
  • 3.3. In the presence of 5% CO2 there were no significant changes in carbohydrate utilization and acid production.
  • 4.4. Aerobiosis was accompanied by increased carbohydrate utilization and end product formation. No Pasteur effect could be observed.
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16.
  • 1.1. Studies characterizing glucose transport in the frog sartorius were performed.
  • 2.2. For nonstimulated and stimulated muscles, intracellular 2-deoxyglucose exceeded 2-deoxyglucose-6-phosphate at 15 min, showed little further increase, and was maintained below the extracellular concentration for 2 hr.
  • 3.3. Accumulated 2-deoxyglucose-6-phosphate did not inhibit glucose transport.
  • 4.4. Unlike in adipocytes, basal and stimulated 2-deoxyglucose transport showed no difference in sensitivity to N-carbobenzoxy-glycyl-l-phenylalaninamide.
  • 5.5. Phenylarsine oxide blocked contraction-enhanced 2-deoxyglucose uptake.
  • 6.6. These results suggest that the glucose transporter of the sartorius exhibits auto-regulation, and that basal transport is not regulated by the same process as in adipocytes.
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17.
  • 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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18.
  • 1.1. To study the temporal organization of energy metabolism in rat liver the steady state concentrations of key intermediates of carbohydrate and phosphorus metabolism were determined during 24 hr.
  • 2.2. The circadian rhythm in energy metabolism of rat liver has been analysed by four different approaches. It was shown that neither apparent PEP synthesis nor crossover theorem were acceptable for the elucidation of the temporal organization of multi-enzyme systems.
  • 3.3. Correlations analysis explained the temporal organization of energy metabolism most satisfactorily.
  • 4.4. Based on the results of this analysis it was suggested that circadian regulation of energy metabolism in liver was realized at the level of the citric acid cycle.
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19.
  • 1. Hemolysates from 16 species of Amazon fish and one amphibian were analyzed by gel electrofocusing. The change in isoelectric point upon deoxygenation provided a reliable estimate of the Bohr effect.
  • 2. Certain species of fish had single hemoglobin components whose pI increased significantly upon deoxygenation, as in man. Other fish had hemoglobins whose isoelectric points were unaffected by deoxygenation. Six species of fish had at least two hemoglobin components, one of which had a reduced isoelectric point upon deoxygenation indicating a reversed Bohr effect, whereas the other(s) had an increased isoelectric point on deoxygenation, as occurs with the normal alkaline Bohr effect.
  • 3. A close correlation was found between the change in isoelectric point with deoxygenation and the Bohr effect determined by oxygen equilibrium measurements.
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20.
  • 1.1. Proteins from crystalline styles of twelve species of bivalve mollusc were examined under different gel electrophoresis conditions and stained to reveal both protein and carbohydrate.
  • 2.2. Native extracts of styles produced relatively few protein bands, however denaturation with SDS resulted in much more complex zymograms.
  • 3.3. All species possessed several prominent high mol wt glycoproteins.
  • 4.4. Eulamellibranchia all had a major non-glycosylated protein at approx. 62,000 mol. wt.
  • 5.5. Most Filibranchia had a major non-glycosylated protein at 37,000–50,000 mol. wt.
  • 6.6. Eulamellibranchia were a much more homogeneous group than the Filibranchia.
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