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1.
  • 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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2.
  • 1.1. Activities of the red and white muscle LDH from 8°C-acclimated goldfish were about three times higher than those acclimated to 28°C.
  • 2.2. Isozyme composition and some kinetic properties of the red muscle LDH differed from those of the white muscle enzyme.
  • 3.3. The amount of red muscle as well as LDH activity tended to increase during cold acclimation.
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3.
  • 1.1. The participation of an environmental factor such as photoperiod in the metamorphic development of Discoglossus pictus has been studied.
  • 2.2. Short photoperiods were more effective in accelerating the rate of growth and the stages of development of tadpoles than were long photoperiods.
  • 3.3. Daily melatonin injections to tadpoles during larval development showed different effects depending on the artificial photoperiod in which the tadpoles were maintained.
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4.
  • 1.1. γ-Glutamyltranspeptidase is present in echinoderm eggs and larvae: in homogenates the level of activity is comparable to that of rat cerebral cortex.
  • 2.2. In eggs of Lytechinus pictus, fertilization induces an early rapid and sustained (5 min–6 hr) 37% increase in the activity of γ-glutamyltranspeptidase in homogenate fractions.
  • 3.3. Relative to these homogenate levels, the specific activity of γ-glutamyltranspeptidase are ≈60% lower in 40,000 g supernatant fractions and 2.7-fold higher in 40,000 g particulate fractions in both unfertilized and 15 min post-fertilized Lytechinus pictus eggs.
  • 4.4. The subcellular distribution of γ-glutamyltranspeptidase is the same in both unfertilized and 15-min post-fertilized Lytechinus pictus eggs: 78% in 40,000 g particulate fractions, 22% in 40,000 g soluble fractions.
  • 5.5. In both unfertilized and 15 min post-fertilized eggs of Lytechinus pictus the enzyme responds to heat (50 vs 37°C) by activation in a similar manner: 1.72- and 1.68-fold homogenates; 2.6- and 3.0-fold in supernatants; 1.97- and 1.90-fold in particulate fractions.
  • 6.6. In homogenates of Pisaster ochraceous larvae, γ-glutamyltranspeptidase activity increases steadily during the course of larval development: relative to the low activity at day 5, activities exhibit an increase of 1.2-, 2.0-, 3.1- and 5.4-fold at days 10, 16, 22 and 28, respectively.
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5.
  • 1.1. Differential thermal acclimatory responses of maximal catalytic rates (Vmax) of digestive enzymes have been measured in both sexes of Periplaneta americana adapted to 16 and 32°C.
  • 2.2. Salivary amylase of females and gastric protease of males exhibit “translational” acclimation, the former showing a “complete” but the latter only a “partial” compensation. The value of Q10 is not altered in the adaptive response.
  • 3.3. An alteration of the thermal coefficient is evidenced by the “translational-cum-rotational” compensation of gastric amylolytic activity, with significant warm acclimation but no cold acclimation in both sexes.
  • 4.4. Gastric protease of female cockroaches and gastric lipase of both sexes are characterized by the lack of an adaptive compensation to temperature, while salivary amylase of male appears to manifest an “inverse” acclimation.
  • 5.5. Sexual dimorphism in the levels of the activities and in the patterns of thermal acclimation of the digestive enzymes is indicated.
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6.
  • 1.1. Preparation, purification and characterization of a phosphoglycolate phosphatase (PGP)3 isoenzyme from human erythrocytes was achieved by DEAE-Sepharose CL.-6B chromatography and isoelectric focusing using carrier ampholytes. pH 4–6.
  • 2.2. The isoenzyme has an isoelectric point of 5.00 ± 0.05 and could be purified 33.000 fold to a specific activity of 32.7 U/mg of protein. It represents the PGP phenotype 1 consisting of a single isoenzyme.
  • 3.3. The enzyme is composed of two subunits (mol. wt 35,000) which are identical and not connected by SS-bridges.
  • 4.4. At 4°C the isoenzyme is more stable in the pH range of 7–9 than at acid pH values.
  • 5.5. Incubation at 30 and 40°C for 4 hr does not affect the activity of the isoenzyme.
  • 6.6. It has a Km-value of 0.28 mM for phosphoglycolate (PG) as substrate.
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7.
  • 1.1.|The standard metabolic rates (SMRs) and preferred body temperatures (PBTs) of the tropical cordylid Cordylus jonesi and temperature lacertid Lacerta lilfordi were determined following acclimation to constant environmental temperatures of 20 and 30°C.
  • 2.2.|Although after 5 weeks the SMRs of Cordylus jonesi and Lacerta lilfordi displayed partial compensations of 20.9 and 10.5%, respectively, their PBTs did not alter over this period. Therefore, acclimation does not maintain complete metabolic homeostasis during either the active or inactive phase of the lizard.
  • 3.3.|Cordylus jonesi allowed to thermoregulate behaviourally at their PBT during activity possessed similar SMRs to control animals maintained continually at the same background temperatures, indicating that acclimation state in lizards is determined by the body temperatures experienced while at rest.
  • 4.4.|The particular acclimatory problems of animals exhibiting behavioural homeothermy are discussed.
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8.
  • 1.1. Cardiac frequency patterns of Callincctes sapidus Rathbun were used to evaluate potential thermal stress after exposure to 5°C increases over a range of acclimation temperatures from 5° to 30°C.
  • 2.2. An acclimated rate-temperature curve (R-T curve), acute R-T curves of the stabilized rates at the increased temperatures and Q10 temperature coefficients were used to assess the significance of the changes in rate frequency.
  • 3.3. The acclimated R-T curve showed that blue crabs go through a series of seasonal adaptation types characterized by a plateau of perfect adaptation for both cold and warm adapted organisms. Paradoxical adaptation occurred between the transition from cold to warm acclimation temperatures.
  • 4.4. The acute R-T curves showed that cardiac frequency was highly responsive to a 5°C increase when the organisms were acclimated to low temperatures.
  • 5.5. The Q10's of the acute R-T curves at the warm acclimation temperatures approximated those values derived for the acclimated R-T curve.
  • 6.6. This suggests that the temperature increase had a negligible effect on the warm adapted crabs, that is, little or no thermal stress occurred.
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9.
10.
  • 1.1. The effect of acclimation to 10° and 30°C on the blood volume, clotting time, total blood protein and numbers of cells was determined in Uca pugilator.
  • 2.2. There was no significant difference between blood volume in the 10° and 30° animals but there were significantly more cells and a higher blood protein in the 30° crabs.
  • 3.3. The clotting time is significantly longer for the 10° crabs.
  • 4.4. These changes associated with the blood parameters can be associated with the ecology of the animal.
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11.
  • 1.1. Electrical stimulation and DOPA decarboxylase activities were studied in Crassostrea virginica maintained at 30‰ habitat salinity.
  • 2.2. Exposure to light significantly reduced the effectiveness of the electrical stimulation and 30‰ habitat acclimation. However, periods of exposure to darkness had the opposite result. Recovery to the 30‰ habitat ctenidial ciliary rate was significantly faster (more than 2 × ) in animals dissected and then maintained in darkness during the acclimation period.
  • 3.3. Acclimation time of dark-dissected ctenidial preparation was significantly increased in the presence of A-23187 (a calcium cell membrane pore facilitator) or PTZ (a cytosomal calcium releasor). The latter treatment exhibited only about a 65% recovery to the control basal rate of beating.
  • 4.4. This study elucidates a cytosomal role in the acclimation process via a neuronal regulatory mechanism controlling ciliary activity on the ctenidium. Cytosomes could conceivably furnish an extension of the transport activity of the plasma membrane to bring about a sophisticated microscopic control of solute (i.e. calcium) homoeostasis in the cytosol.
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12.
  • 1.1. Opine dehydrogenases (OpDHs) and lactate dehydrogenase (LDH) activities were determined in various marine animals. OpDHs were detected in six marine invertebrate phyla; Porifera, Coelenterata, Annelida, Mollusca, Arthropoda and Echinodermata in phylogenic sequence.
  • 2.2. Among several OpDHs, tauropine dehydrogenase (TaDH) occurred widely in marine invertebrates, from Porifera to Echinodermata.
  • 3.3. With a few exceptions, total OpDHs activities exceeded that of LDH activity in the marine invertebrates investigated.
  • 4.4. With respect to anaerobic glycolysis, OpDHs are indicated to play an important role in phylogenically lower invertebrates, whereas LDH is more important in higher animals.
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13.
  • 1.1. Free amino acids were analysed in the haemolymph of Galleria mellonella larvae by HPLC chromatography with o-phthaldialdehyde (OPA)-l-thio-β-d-glucose as derivatization agent.
  • 2.2. Fourteen primary amino acids were detected among which glutamine, alanine, γ-aminobutyric acid (GABA) and glycine predominated and constituted 67.7% of the amino acids found.
  • 3.3. The concentration of GABA increased significantly with the age of larvae entering the wandering phase and reached a maximum during metamorphosis.
  • 4.4. Analysis of cold-acclimated larvae revealed a net increase of free primary amino acids from 96 to 151.8 μmol/ml during consecutive acclimation to 0°C within 20 days and to 205.4μmol/ml during cold shock injury at 0°C (3 hr).
  • 5.5. The bulk of this increase was accounted for by alanine, glycine, phenylalanine and lysine.
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14.
  • 1.1. The role of the visceral nerve in mediating the changes in heart rate associated with different behavioral patterns was investigated in Megalobulimus sanctipauli.
  • 2.2. The results of acute and chronic denervation experiments indicate that the visceral nerve has no excitatory or inhibitory tonic action on the heart of snails retracted into the shell, nor does it account for the increase in heart rate associated with the locomotion and feeding behaviors.
  • 3.3. These changes in heart rate are, probably, indirect effects of increased activity such as an increase in venous return.
  • 4.4. The visceral nerve is responsible for approximately 3/4 of the increase in heart rate associated with the first minute of extrusion.
  • 5.5. The small increase in heart rate observed in denervated animals is probably caused by an increase in venous return generated by muscle activity that forces the head and food out of the shell.
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15.
  • 1.1.|Intraspecific variation in the thermal physiology of Rana sylvatica was examined.
  • 2.2.|Heat and cold tolerances of both adult and larval representatives were determined for animals representing populations from New York, Maryland, Kentucky, Ohio, Michigan and Canada.
  • 3.3.|In general, frogs from more northern localities exhibited lower heat tolerances.
  • 4.4.|There was no evidence of interpopulational differences in cold tolerance. Similar trends were revealed by larval testing.
  • 5.5.|Interpopulational differences among laboratory-reared tadpoles suggests a strong genetic component to Rana sylvatica thermal physiology.
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16.
  • 1.1. To evaluate changes in high-energy phosphate metabolism in the water scorpion (Ranatra chinensis) under restraint and cold water-warm water stresses, in vivo [31P]NMR spectra were obtained.
  • 2.2. Under restraint stress, arginine phosphate (Arg-P) decreased by 10% after 1 hr and remained at that level thereafter, while β-ATP showed negligible changes over 6 hr.
  • 3.3. As the water temperature gradually increased or decreased, the relative concentration of Arg-P decreased due to enzyme regulation.
  • 4.4. Repeated cold water-warm water stress, which consisted of repeated 15 min exposures to cold water (5°C) followed by 15 min exposures to warm water (30°C) caused distinct decreases in Arg-P and β-ATP concentration. These decreases were dependent on the frequency of exposure.
  • 5.5. Phosphomonoesters (PME) increased not only with restraint stress but also with cold water-warm water stress.
  • 6.6. The effect of cold water-warm water stress on high-energy phosphate metabolism was greater than that of restraint stress.
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17.
  • 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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18.
  • 1.1. The mean Km and Vmax values for G3PDH isolated from the lateral muscle of cold-adapted (5°C) rainbow trout, Salmo gairdneri, were twice those of enzyme from warm-adapted (15°C) trout when assayed at 7°C but not at any other temperature.
  • 2.2. The entropy of activation of warm enzyme was about 3 times that of cold enzyme. However, enthalpy or free energy of activation among acclimation groups differed less or not at all.
  • 3.3. Individual G3PDH isolates within either adaptation group differed in kinetic characteristics.
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19.
  • 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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20.
  • 1.1. Orchestia gammarellus maintained in air and provided with food in the form of agar was found to be very tolerant of changes in the ionic content of the food and was shown to have well-developed powers of ionic regulation over the salinity range 5–40‰ at 10°C.
  • 2.2. There was an inverse relationship between haemolymph protein and acclimation salinity.
  • 3.3. The concentration of sodium and protein ions in the haemolymph of O. gammarellus from above high water mark (H.W.M.) was markedly different from animals collected below H.W.M. Individuals taken from above H.W.M. characteristically had low haemolymph sodium but elevated haemolymph protein concentrations.
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