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1.
  • 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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2.
  • 1.1. In great-horned owls food metabolizability, food intake and body weight were not significantly affected by cecectomy.
  • 2.2. Following cecectomy, water ingestion increased.
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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. The ionic composition and amino acid content of the flexor muscles of seven species of decapod crustaceans have been investigated under defined conditions.
  • 2.2. Haemolymph of the same animals has also been analysed.
  • 3.3. The results show that muscle tissue of these animals has substantially similar intracellular ionic concentrations but widely varying water contents.
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5.
  • 1.1. Subcellular distribution of (NA+, K+-ATPase and ouabain-insensitive ATPase (Mg2+-ATPase) are compared in branchial tissues of the euryhaline crab, Eriocheir sinensis, acclimated to fresh water.
  • 2.2. Both the anterior and posterior gills contain cAMP-dependent protein kinase and endogenous protein substrate for phosphorylation.
  • 3.3. Phosphorylation occurs in both “particulate” and “soluble” subcellular fractions but its stimulation by cAMP is restricted to the “soluble” fraction.
  • 4.4. serotonin (5-HT) and dopamine receptors are present only in the “light particulate” fraction isolated from the posterior gills.
  • 1.(a) Serotonin and dopamine have no effect on the phosphorylation observed in a subcellular fraction alone.
  • 2.(b) Activation of the phosphorylation by serotonin and dopamine is found when the soluble fraction (source of cAMP-dependent protein kinase) is added to the fraction P3 from the posterior gills.
  • 3.(c) No activation occurs with the fractions P3 as well as P1 or P2 (not shown) from anterior gills of fresh water crab.
  • 4.(d) Cyproheptadine, a serotonin receptor antagonist, inhibits the 5-HT dependent increase in phosphorylation.
  • 5.(e) The dopamine receptor antagonist, chlorpromazine, inhibits dopamine-stimulated phosphorylation.
  • 6.5. Ouabain mimics the effect of cyproheptadine on the serotonin-stimulated phosphorylation found in the posterior gills.
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6.
  • 1.1. The effects of 2% saline imbibition and water deprivation on the water balance of the gerbil were compared.
  • 2.2. The unchanged fluid intake and losses, body weight and several blood indices suggested little alteration in the state of hydration after saline imbibition.
  • 3.3. After 5 days water deprivation the animals lost weight and evidence of haemoconcentration was observed. These changes took place despite reductions in water loss (via the urine and faeces) and evidence of secretion of vasopressin and the two principal acidic neural lobe proteins.
  • 4.4. The gerbil appeared to be better adapted to water stress induced by saline imbibition than by water deprivation and this may be related to its habitat in Northern Asia.
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7.
  • 1.1. Blood volume and plasma biochemical changes and feed and water consumption in response to a hemorrhage by phlebotomy of 30% of the calculated total blood volume with and without replacement of blood volume with physiological saline were determined in juvenile male Coturnix coturnix japonica.
  • 2.2. Plasma protein and osmolality decreased rapidly posthemorrhage and did not recover by 72 hr posthemorrhage.
  • 3.3. Plasma glucose, Na+ and K+ increased within Ihr postphlebotomy. Plasma Na+ returned to nonphlebotomized levels within 6 hr postphlebotomy.
  • 4.4. Saline replacement of blood volume resulted in hypervolemia within 3–5 min postphlebotomy.
  • 5.5. Phlebotomized quail receiving no saline recovered blood volume to 0 hr (nonphlebotomized) levels within l hr postphlebotomy.
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8.
  • 1.1. Organ weight studies were carried out on young and aged mice of the Goodale Giant Strain (G/Gw).
  • 2.2. G/Gw mice have increased body weight (over 40 g), but are normally proportioned without any evidence of obesity.
  • 3.3. Most organ weights of the G/Gw increased in direct proportion to the increase in body weight although the pituitary, liver and kidneys exhibited relatively larger sizes than in normal sized studies.
  • 4.4. The increase in liver weight was found to be associated with an increased level of liver glycogen.
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9.
  • 1.1. Guppies exposed to several triphenyltin chloride (TPTC) concentrations in water died as soon as a body burden of 20 ± 10 nmol/g fish was reached.
  • 2.2. Accumulation of TPTC during exposure in acute toxicity experiments can be predicted by using the kinetic parameters of TPTC.
  • 3.3. The lethal body burden is two orders of magnitude lower than for narcotic organic compounds such as chlorobenzenes.
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10.
  • 1.1. Changes in body composition during starvation were compared between germ-free (GF) and conventionalized (CVL) chicks in experiment 1. At 8 days of age, the GF birds were divided into two groups, i.e. GF and CVL groups. The CVL birds were inoculated with faeces from conventionally reared birds. Until 14 days of age, both birds were fed a diet ad lib, and thereafter starved for 6 days.
  • 2.2. Nitrogen loss during starvation was significantly lower in CVL birds, though the reverse was true for water loss. Fasting heat production was comparable between two environments.
  • 3.3. Influence of the gut microflora on body weight and nitrogen losses during starvation was investigated in birds prefed diets high or low in dietary protein in experiment 2.
  • 4.4. No significant effect of the gut microflora was observed in body weight and nitrogen losses. Body weight was severely reduced in birds prefed the high protein diet and nitrogen loss was lower in birds prefed the low protein diet.
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11.
  • 1.1. The effects of alternating current electronarcosis, rectified current electronarcosis and chemical anaesthesia (benzocaine hydrochloride) on plasma electrolytes and on the osmotic pressure of the blood of the freshwater bream Oreochromis mossambicus were evaluated.
  • 2.2. Plasma Ca2+, Na+ and K+ concentrations and the osmotic pressure of the blood were monitored over a period of 7 days.
  • 3.3. The results showed that the different electrolytes respond differently to the different techniques.
  • 4.4. Chemical anaesthesia exhibited the least effects on the parameters studied.
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12.
  • 1.1. Plasma concentrations of urea, uric acid and total lipid were compared in pre- and late-fast breeding and moulting macaroni penguins (Eudyptes chrysolophus) to test the hypothesis that birds exhaust their lipid reserves and initiate marked protein utilisation towards the end of natural fasts.
  • 2.2. Male and female macaroni penguins fasted for a minimum of 29–32 days and 20 days during the breeding and moult fasts, and the difference in body weight over the sample period (reflecting body weight loss) was 31–34% and 41–47%, respectively.
  • 3.3. There was no significant increase in plasma urea or uric acid at the end of either fast, nor any decrease in plasma lipid concentrations compared to pre-fast birds.
  • 4.4. These results suggest that macaroni penguins continue to rely mainly on lipid reserves during the later stages of natural fasts. This is consistent with post-fast body composition data for other small penguin species.
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13.
  • 1.1. Hatching Caretta caretta may lose up to 12% of their initial hatched weight from water loss during emergence from the nest.
  • 2.2. After subsequent osmotic and excretory water loss in sea water, hatchlings will drink sea water (166 μl 100 g−1 hr−1) and return to their initial weight within 10–15 days, without feeding.
  • 3.3. There were no significant changes in plasma osmolarity or sodium levels over this period.
  • 4.4. This osmoregulatory strategy is in marked contrast to that seen in the estuarine crocodile, Crocodylus porosus.
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14.
  • 1.1. Total body water volume (TBWV) and daily water turnover rates (WTR) were measured in nestling and adult zebra finches using tritiated water (TOH).
  • 2.2. TBWV and daily WTR increased with age up to 13 days post hatching.
  • 3.3. TBWV and WTR approached adult levels after 13 days of age. WTR varied among ages and nest mates. All nestlings turned over at least 50% of their body water pool per day.
  • 4.4. The WTR data for adult birds are consistent with natural history data suggesting zebra finches are dependent on water for breeding and survival.
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15.
  • 1.1. Kidney, oesophagus and gill Na+-K+ ATPase activity and serum Na+, K+ and Cl concentrations are evaluated in European sea bass during experimental acclimation to fresh water.
  • 2.2. Kidney and oesophagus ATPase increase in low salinity and reach a maximum in fresh water.
  • 3.3. Gill ATPase decreases during the acclimation trials and rises again to normal values after a 3-week stay in fresh water.
  • 4.4. Na+ and K+ serum concentrations decrease during the trials and increase back after a 3-week stay in fresh water.
  • 5.5. The correlations between enzymatic activities, serum ion concentrations, morphological changes and environmental salinity are discussed.
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16.
  • 1.1. A 12 week program of treadmill exercise (0.7 m/sec, 30 min per day, five days per week), significantly increased the myoglobin concentration of the femorotibialis medius muscle in bar-headed geese as compared to nonexercised controls.
  • 2.2. The myoglobin concentration differed among various muscles within a bird. The highest myoglobin concentrations were found in the primary flight muscle, the pectoralis major, and in cardiac muscle.
  • 3.3. By physically conditioning their muscles, bar-headed geese may improve the oxygen flow to mitochondria and, thereby, enhance their ability to exercise under conditions of low oxygen partial pressures.
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17.
  • 1.1. Intracellular pH buffering capacity of hagfish (Eplatretus cirrhatus) dental plate retractor muscles is among the highest reported for any vertebrate muscle.
  • 2.2. Over 80% of the pH buffering capacity of hagfish retractor and myotome muscle is due to components other than proteins and phosphate.
  • 3.3. The muscles have less than 0.5 μmol/g wet weight of l-histidine, and lack l-l-methyl histidine, l-3-methyl histidine and the histidine-containing dipeptides anserine, carnosine and ophidine.
  • 4.4. Instead, they contain an unidentified low molecular weight acid-soluble compound to which the high pH buffering capacity can be attributed.
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18.
  • 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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19.
  • 1.1. Freshwater limpets were fed [14C] labelled food for 24hr, and unlabelled food for 96hr.
  • 2.2. Incorporation into the periostracum was on average about 6.8% of total soft body value.
  • 3.3. A negative correlation exists between the absolute amount incorporated into the soft body and the per cent incorporation into the periostracum.
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20.
  • 1.1. Gilthead sea breams (Sparus aurata L.) adapted to sea water (SW, 39‰ salinity) and brackish water (BW, 7‰) were submitted to abrupt osmotic stress by transferring the specimens to 7‰ and 39‰, respectively.
  • 2.2. Plasma osmolality, Na,+ Cl, K, + Ca, 2+ cortisol and glucose were measured before and after the transfers.
  • 3.3. The transfer from SW to BW led to transitory hypomineralization and hyperglycemia. In long-term adapted fish cortisol level increased, and osmolality slightly decreased.
  • 4.4. Conversely, the transfer from BW to SW provoked transitory hypermineralization. In adapted fish, cortisol levels strongly decreased, and osmolality slightly increased.
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