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1.
  • 1.1. Carp red cells were treated with drugs that affect the cell membranes. The water content of the cells and the accumulation of cAMP in the cells were measured in normoxia and in hypoxia using non-stimulated and adrenergically stimulated cells.
  • 2.2. WGA, DIDS + CCCP and A23187 increased the water content of nonstimulated normoxic cells.
  • 3.3. In hypoxia ouabain and DIDS + CCCP increased the water content but cytochalasin B, NPM, DIDS, CCCP and A23187 + CA2+ abolished the hypoxia-induced swelling.
  • 4.4. Any membrane perturbation induced some cAMP formation, Sophora and Anquilla lectins being most potent.
  • 5.5. Also in adrenergically stimulated cells, membrane perturbation generally increased cAMP formation.
  • 6.6. However, cAMP accumulation diminished in cells treated with cytochalasin B, CCCP and DIDS + CCCP.
  • 7.7. The adrenergic swelling of carp red cells was reduced in normoxia by DIDS. NPM and CCCP increased the adrenergic swelling in normoxia to hypoxic level.
  • 8.8. In hypoxia WGA and Anquilla lectin decreased the swelling.
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2.
  • 1.1. Immature carp were subjected to 2-month fasting periods. Mobilization of reserves in liver and muscle, and the energy contribution of each reserve were studied. Changes in plasma glucose, amino acids, insulin and glucagon levels were determined throughout the experiment.
  • 2.2. No changes were observed in plasma glucose, insulin or glucagon at 19 days of fasting, but plasma amino acids increased. At 50 days of fasting, both plasma glucagon and amino acids increased, liver glycogen decreased and muscle proteolysis began.
  • 3.3. Between 50 and 67 days of fasting, plasma glucose and insulin decreased significantly, while glucagon and amino acids continued to increase. Strong muscular proteolysis was observed while liver glycogen stabilized.
  • 4.4. The contribution of each reserve in liver and muscle to energy production throughout fasting is considered.
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3.
  • 1.1. Rainbow trout were acclimated to salt water (1.5, 2.0 or 3.0%, which means 40, 60 or 85% concentrated sea-water) and the electrolyte, glucose and cortisol concentrations of the plasma as well as the extra- and intracellular muscle space, the muscle electrolyte concentrations and the ATPase activity were analysed.
  • 2.2. Plasma osmolality, Na+, Ca2+ and Mg2+ concentrations of the plasma had a maximum at 24 hr after the start of acclimation when acclimated to 3.0% salt water. Plasma osmolality, Na+ and Mg2+ concentrations were significantly higher during the whole acclimation time when exposed to 3.0% salt water.
  • 3.3. Variations and regulations of ECS and ICS were clearly demonstrated. The intracellular electrolyte concentrations were also maximal at 24 hr.
  • 4.4. The plasma glucose level was just slightly elevated, but the cortisol level clearly indicated a stress response at 24 hr.
  • 5.5. The activity of gill Na-K-ATPase increased during the acclimation time.
  • 6.6. The regulatory processes in trout during acclimation to salt water are compared with those occurring in tilapia and carp.
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4.
  • 1.1. Cutaneous O2 uptake in the carp, Cyprinus carpio, was determined at various water flow rates across the skin (.V) ranging from 2.5 to 40 ml/min, using flow-through respirometers.
  • 2.2. When thickness of water flow was 2mm, cutaneous O2 uptake remained stable (about 3.8 nmol/cm2/min) at a .V of 20–40 ml/min and decreased with .V below 20 ml/min.
  • 3.3. When thickness of water flow was 4 mm, cutaneous O2 uptake decreased with .V below 40 ml/min.
  • 4.4. Apparent water velocity (U') was calculated dividing .V by an area of a cross section of the water flow (0.5 and 1.0 cm2 respectively). In both experiments, cutaneous O2 uptake decreased with U' below 0.7 cm/sec.
  • 5.5. This suggests that cutaneous O2 uptake in the carp is limited at a low water velocity by a resistance of the hypoxic boundary layer.
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5.
  • 1.1. Estimation of gonadotropin content of five batches of carp pituitaries by three assay systems yielded similar relative potencies. The assays differed in their estimates of absolute pituitary gonadotropin content.
  • 2.2. Carp gonadotropin was found to be more potent than salmonid gonadotropins in a bioassay based on cyclic AMP accumulation in immature grass carp ovary.
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6.
  • 1.1. Twelve Large White × Landrace male pigs, six with high adrenocortical response to ACTH, and six with low response, were subjected to mild and moderate exercise, and then to insulin-induced hypoglycaemia.
  • 2.2. Plasma ACTH, cortisol, catecholamines and some haematological and plasma biochemical parameters were determined in response to exercise, and glucose and cortisol in response to insulin challenge.
  • 3.3. High responders had significantly greater increases than low responders in ACTH, cortisol and catecholamines following exercise, and in cortisol following insulin challenge.
  • 4.4. The results suggest that differences in adrenocortical response to exogenous ACTH are an accurate reflection of the animal's response to stressful stimuli.
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7.
  • 1.1. DNase-I-like activity occurs in the carp (Cyprinus carpio) liver cytosol (supernatant 105,000g).
  • 2.2. The enzyme resembles DNase I from bovine pancreas in respect to the molecular mass (~31 kDa), pH (7.4) and ion requirements (Mg2+, Ca2+) and the ability to degrade native as well as denatured DNA.
  • 3.3. As judged by comparison of DNase zymograms obtained after native- and SDS-PAGE, the enzyme occurs in the three molecular forms of similar molecular weight and different charges.
  • 4.4. All these forms are inhibited by rabbit skeletal muscle actin as well as by endogenous actin isolated from the carp liver cytosol.
  • 5.5. DNase from the carp liver cytosol does not interact with the antibodies directed against DNase I from bovine pancreas and against DNase I from the rat and bovine parotid glands.
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8.
  • 1.1. Flounders transferred abruptly from sea to fresh water displayed a gradual decrease in plasma osmolality for 5–6 days (10–15 mOsm daily). When returned to sea water the osmolality increased to the original level within 1 day.
  • 2.2. Heart ventricle cell water content remained unchanged during the acclimations, except for a temporary 1.4% reduction within the first 4 hr of sea water acclimation.
  • 3.3. During acclimation to sea water intracellular K+ increased rapidly in parallel with plasma osmolality. During fresh water acclimation, however, cellular K+ decreased rapidly in the first day only, whereas plasma osmolality decreased further.
  • 4.4. Cellular taurine remained unchanged during the initial 4 days of fresh water acclimation and then declined 32% within the next 3 days. Upon retransfer to sea water, cellular taurine increased gradually to its original level in the course of 7 days.
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9.
  • 1.1. Lactating ewes were treated with mouse epidermal growth factor (EGF) at a dose rate of 0.5 mg/day for 4 days and its effects on the electrolyte profile were observed.
  • 2.2. There was no effect of EGF on plasma concentrations of sodium or potassium, although urinary and total (in urine and milk) losses of both were reduced.
  • 3.3. EGF-induced hypocalcaemia was associated with reduced milk calcium secretion and increased urinary calcium excretion whereas EGF-induced hypermagnesaemia was associated with reduced urinary and total magnesium losses.
  • 4.4. Glomerular filtration rate was reduced during EGF infusion.
  • 5.5. Chronic intravenous EGF infusion affects the electrolyte profile by altering electrolyte secretion by the mammary gland and renal electrolyte excretion.
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10.
  • 1.1. The intestinal absorption of insulin in carps was assessed examining the transepithelial passage of ingested gold-labeled hormone by electron microscopy. Insulin transfer occurred mainly through the intercellular spaces between the enterocytes.
  • 2.2. When reaching the lamina propria, the gold-labeled hormone gathered predominantly around the granules of the granular cells, and therefore can enter the circulatory system via the blood capillaries which are found in close contact with these cells.
  • 3.3. Winter-acclimatized carp were also capable of internalizing the hormone when fed with insulin.
  • 4.4. Furthermore, the absorbed hormone revealed full activity in regard to the observed changes in the ultrastructure of the liver cells of the treated cold-adapted fish.
  • 5.5. The fish ingesting the hormone underwent the same type of hepatic ultrastructure reprogramming observed when winter-acclimatized carps are injected intraperitoneally with insulin, i.e. conversion to a phenotype corresponding to hepatocytes from summer-adapted carp.
  • 6.6. The oral absorption of insulin by winter-acclimatized fish and its effect in reversing the cold-adaptive state might be useful for the fish culturing industry.
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11.
  • 1.1. Water absorption response (WR) behavior and water weight gain were examined in hydrated toads, Bufo woodhousei, treated with angiotensin II (All) or with a control Ringer's solution. The effects of urinary bladder condition (ad lib. bladder urine or empty bladder) were examined concurrently.
  • 2.2. Toads treated with All (100μg/100g body weight), spent more time in WR posture and absorbed more water than Ringer's-injected toads.
  • 3.3. Toads with empty bladders maintained WR posture for longer periods of time and gained more weight than toads whose bladders were not emptied.
  • 4.4. The effects of All and bladder urine on water absorption by B. woodhousei appear to be separate and additive.
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12.
  • 1.1. The cytogenetic effects of various i.p. treatments with five carcinogenic-mutagenic chemicals and three doses for each (aflatoxin Bl, Aroclor 1254, benzidine, benzo[a]pyrene and 20-methylcholanthrene), were investigated in the cells of the common carp, Cyprinus carpio.
  • 2.2. Injection with distilled water and corn oil served as the two control groups.
  • 3.3. For detecting cytogenetic damage we used two test systems, chromosomal aberrations (CA) in kidney cells and micronucleated erythrocytes (M).
  • 4.4. At 48 hr after treatment with the chemicals under investigation, the frequencies of CA and M were clearly increased in a dose-response manner compared to the control groups.
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13.
  • 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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14.
  • 1.1. The major metabolic changes associated with repeated capture, aquarium transfer, anaesthesia and blood sampling were investigated in an Australian freshwater fish, the golden perch (Macquaria ambigua),
  • 2.2. A compounded stress response was seen after repetition of the procedure, in which the plasma glucose rose within 3 hr and amino acid concentrations rose and the serum free fatty acids concentration fell after 24 hr.
  • 3.3. Alanine was identified as an important circulating energy store in the stress response of golden perch.
  • 4.4. No change was noted in the serum protein, plasma lactate or β-hydroxybutyrate concentrations, indicating that tissue damage and hypoxia were absent, and that degradation of free fatty acids did not produce metabolites excess to the requirements of gluconeogenesis and the tricarboxylic acid cycle.
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15.
  • 1.1. The biochemical characteristics of homogenates and mitochondria isolated from the outer and inner layers of the ventricular myocardium of carp were studied.
  • 2.2. The homogenate prepared from the inner layer exhibited higher activity of cytochrome oxidase than that from the outer layer. No difference was found in the activity of cytochrome oxidase between mitochondria from the inner and outer layers. Difference spectra of cytochromes also showed that their content in mitochondria of both layers is similar and that the higher oxidative capacity of the spongious layer is due to a higher content of mitochondria.
  • 3.3. In comparison with rat heart a higher content of cyt aa3 and a lower content of Cyt b and cyt cc1 were found in carp heart mitochondria.
  • 4.4. In comparison with rat heart, carp heart mitochondrial enzymes were more sensitive to freezing-thawing and to detergent action.
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16.
  • 1.1. Changes in urine and plasma concentrations (sodium, potassium, magnesium, calcium and total osmotic) and urine production were determined in fish exposed to various concentrations of an ionically active substance, sodium chloride, and a non-electrolyte, mannitol, as well as freshwater.
  • 2.2. Responses occurred for the most part over a short crisis period preceeding establishment of new stable conditions.
  • 3.3. It was shown that plasma homeostasis was not maintained in response to changing ion-osmotic and osmotic gradients.
  • 4.4. Urinary osmotic and ionic concentrations were unaffected and urine production was shown to be inversely related to the external concentration.
  • 5.5. It is suggested that ionic shifts between body compartments are an important aspect of ion-osmotic adaptation.
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17.
  • 1.1. Oxygen uptake attributable to Specific Dynamic Action (SDA) was measured in common carp, Cyprinus carpio L. (63.6–84.0 g) fed on 20, 35 and 50% dietary protein at 0.40 to 1.00% ration levels at 28°C.
  • 2.2. After feeding both SDA magnitude and mean peak oxygen consumption increased directly with dietary protein and ration levels. SDA duration was not significantly related to dietary protein but significantly increased with ration levels.
  • 3.3. SDA coefficients were 8.99, 13.51 and 15.94% with 20, 35 and 50% dietary protein showing a direction relationship to the protein content. The SDA coefficient did not change with ration size.
  • 4.4. SDA models resulting from this work are of great interest for the aquaculturist, as post-feeding oxygen requirements in an intensive fish culture can be predicted where dietary protein and ration levels are known.
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18.
  • 1.1. The capacity of five anuran Amphibians (Bufo viridis B. regularis, Rana ridibunda, Hyla arborea and Pelobates syriacus) to acclimate to NaCl and urea solutions was investigated.
  • 2.2. All species could be acclimated to relatively high concentrations of urea solutions, while only Bufo viridis and Hyla arborea could be acclimated to 500 mOsm/kg or higher NaCl solutions.
  • 3.3. The plasma urea concentration in B. viridis and H. arborea was elevated to levels over 140 mmol/1.
  • 4.4. The sum of plasma sodium and chloride concentrations did not increase over 400 mmol/l in any species.
  • 5.5. Urine osmolality, which was normally low, increased, but never exceeded the plasma osmolality.
  • 6.6. In the urea acclimation conditions, urine electrolytes diminished, similarly in all species in this study.
  • 7.7. It is concluded that anuran Amphibians can tolerate high plasma urea concentrations, but only those species which can elevate it, either through retention or net synthesis, can be acclimated to high salt solutions.
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19.
  • 1.1. Common carp (Cyprinus carpio) exposed to experimental temperatures of 12, 18, 24, 30 or 36°C for a 4-week period were used to investigate the effect of temperature acclimation on the frequency of opercular movement (FOM), growth and cytochrome c oxidase (CCO) activity in heart, liver and muscle.
  • 2.2. An exponential relationship between FOM and temperature after the first week (1010 =1.76) disappeared after the second week.
  • 3.3. The initially high FOM at temperatures of 30 or 36°C and the low FOM at 18 or 12°C changed over 4 weeks to approach the FOM of fish at 24°C.
  • 4.4. This change in the relationship of FOM to temperature from highly dependent to independent appeared to be thermal compensation.
  • 5.5. Heart and liver CCO activities were significantly affected by temperature, with the lowest activity at the approximate optimum temperature for growth, 24°C.
  • 6.6. Highest CCO activities for heart and liver occurred at both the highest and lowest temperatures.
  • 7.7. Among the three tissues, heart CCO activity was generally the highest and most affected by acclimation temperature.
  • 8.8. Muscle tissue had the lowest CCO activity and was unaffected by temperature.
  • 9.9. The high CCO activity at a cold acclimation of temperature 12°C was probably due to thermal compensation and the high activity at 36°C may have been a result of thermal stress.
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20.
  • 1.1. The oxygen consumption of crabs in normoxic and hypoxic (50% O2) seawater was measured directly after collection.
  • 2.2. The influences of size and lunar cycles were removed by scaling the data.
  • 3.3. Strong negative correlations between low individual levels of O2 consumption and the ability to compensate for hypoxia were apparent in Wicklow (subtidal) crabs.
  • 4.4. Compensation for hypoxia was much greater on the flood tide than on the ebb.
  • 5.5. Crabs from Roscoff (intertidal) had lower levels of compensation than those from Wicklow.
  • 6.6. Size, sex and condition had no apparent effect upon these relationships.
  • 7.7. Crabs acclimated to laboratory conditions have not shown this tidal variation in compensation for hypoxia.
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