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1.
  • 1.1. Pondwater acclimated Carunculina texasensis and Ligumia subrostrata experienced a 230% increase in Na influx when injected with dibutyryl cyclic AMP (0.4mM/l blood).
  • 2.2. Theophylline, a phosphodiesterase inhibitor, or indomethacin, an inhibitor of prostaglandin (PG) synthetase, caused a dose dependent stimulation of Na transport.
  • 3.3. Prostaglandin E2 injected into mussels caused an inhibition of Na influx. Arachidonic acid, the precursor of PGE2, inhibited Na influx or stimulated Na efflux depending on the animal's acclimation conditions.
  • 4.4. Chloride transport was unaffected by the drugs used in this study.
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2.
  • 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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3.
  • 1.1. The oxygen consumption of Bullia digitalis from South Africa's west coast, measured at a fixed activity level at 15°C, does not differ significantly between winter and summer.
  • 2.2. The adult acute rate-temperature curve is flattened over the temperature range likely to be encountered in the field, there being no significant difference in oxygen consumption between 15 and 22.5°C.
  • 3.3. Below this plateau the Q10 is normal, giving a value of 2.67 between 5 and 10°C, but at temperatures above 22.5°C the Q10 is less than 2 and oxygen consumption at 30°C does not approach that of the tropical Bullia melanoides at the same temperature.
  • 4.4. Both field and laboratory acclimated animals provide evidence that the rate-temperature curve is unaffected by such acclimation, either to high or low temperatures.
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4.
  • 1.1. Some aspects of the gas exchange system of a diving lizard, Physignathus lesuewii were studied.
  • 2.2. Breathing patterns were analysed.
  • 3.3. Breathing rate increases logarithmically with temperature and Q10 = 1.8. LogBR = −0.237 + 0.0256 T.
  • 4.4. Gas tensions in lung air and arterial and venous blood were measured. Arterial pH declines with increasing temperature.
  • 5.5. Temperature has a marked effect on oxygen affinity of the blood (ΔH = −10.1 kcal mol). A Bohr effect was also noted.
  • 6.6. CO2 equilibrium curves were drawn.
  • 7.7. The results are considered with a view to anticipating the efficiency of the gas exchange system of this species under conditions of variable temperature and during diving.
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5.
6.
  • 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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7.
  • 1.1. The decarboxylation of uroporphyrinogens I and III by porphyrinogen carboxy-lyase (EC 4.1.1.37) in mouse liver supernatant was compared in relation to substrate concentrations.
  • 2.2. In this species uroporphyrinogen III was the best substrate judging by the criteria of Km/Vmax (estimated for total porphyrinogens) and was converted into coproporphyrinogen faster than its series I isomer.
  • 3.3. The difference between the two isomers was mainly due to the first decarboxylation.
  • 4.4. This difference was confirmed by calculation of the Hill coefficient and of Lineweaver-Burk plot which suggested that isomer I induced negative cooperativity in the active centre of the enzyme.
  • 5.5. After treatment with a porphyrogenic dose of TCDD (25 μg/kg/week for 9 weeks) differences between uroporphyrinogen I and III as substrate were maintained.
  • 6.6. In addition treatment reduced Vmax and Km (estimated for total porphyrinogens) of liver porphyrinogen carboxy-lyase to about half control values for both isomers.
  • 7.7. Vmax was reduced mainly because of the formation of smaller amounts of all products of decarboxylation, and Km because more heptaporphyrinogen was formed than coproporphyrinogen.
  • 8.8. Values of the Hill coefficient and Lineweaver-Burk plots suggested TCDD induced altered substrate affinity for isomer III too.
  • 9.9. Treatment with TCDD did not affect the decarboxylation of uroporphyrinogen III by RBC porphyrinogen carboxy-lyase, estimated from Km and Vmax for total porphyrinogens formed.
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8.
  • 1.1. To characterize an enzyme which metabolizes retinal in liver microsomes, several properties of the enzymatic reaction from retinal to retinoic acid were investigated using rabbit liver microsomes.
  • 2.2. The maximum pH of the reaction in the liver microsomes was 7.6.
  • 3.3. The Km and Vmax values for all-trans, 9-cis and 13-cis-retinals were determined.
  • 4.4. The reaction proceeded in the presence of NADPH and molecular oxygen.
  • 5.5. The incorporation of one atom of molecular oxygen into retinal was confirmed by using oxygen-18, showing that the reaction comprised monooxygenation, not dehydrogenation.
  • 6.6. The monooxygenase activity was inhibited by carbon monoxide, phenylisocyanide and antiNADPH-cytochrome P-450 reductase IgG, but not by anti-cytochrome b5 IgG.
  • 7.7. The enzymatic activity inhibited by carbon monoxide was photoreversibly restored by light of a wavelength of around 450 nm.
  • 8.8. The retinal-induced spectra of liver microsomes with three isomeric retinals were type I spectra.
  • 9.9. The microsomal monooxygenase activity induced by phenobarbital or ethanol were more effective than that by 3-methylcholanthrene, clotrimazole or β-naphthoflavone.
  • 10.10. These results showed that the monooxygenase reaction from retinal to retinoic acid in liver microsomes is catalyzed by a cytochrome P-450-linked monooxygenase system.
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9.
  • 1. Blood oxygen affinities, erythrocytic nucleoside triphosphate concentrations (NTP) and other hematological parameters were measured in facultative air-breathing fish from the Amazon after acclimation to well-aerated (“normoxic”) and hypoxic water (PO2 = 125–135 and 20–25 mm, respectively).
  • 2. In the armored catfishHypostomus sp. andPterygoplichthys sp., hypoxia induces intermittent surfacing to gulp air and results in lower NTP levels, chiefly through significant decreases in guanosine triphosphate (GTP). The subsequent increases in blood O2 affinity appear adaptive to lowered time average internal O2 tensions. No similar changes were seen in the ellSynbranchus which breathes air almost continuously when kept in hypoxic water.
  • 3. The results are discussed in terms of their adaptive significance, and compared with data on temperate fish.
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10.
  • 1.1. Rates of evaporative water loss (EWL) were measured in Anolis roquet and A. marmoratus each from three localities which varied in conditions of aridity.
  • 2.2. There were significant interpopulational differences in rates of EWL for both species which correlated with habitat aridity.
  • 3.3. Rates of EWL were significantly lower in A. roquet after 6 weeks acclimation to more xeric conditions, populational differences were still evident.
  • 4.4. Acclimational effects on rates of EWL were 2 to 3 times greater than populational differences.
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11.
  • 1.1. The exponent (b) relating metabolic rate to dry weight in excised gills of Tagelus plebeius is not maintained constant throughout the seasons or upon acute exposure to temperatures of 9–34°C.
  • 2.2. Acclimation (11–29°C) and test (9–34°C) temperatures have a significant effect (α = 0.01) on the mean rate of oxygen uptake by the gills.
  • 3.3. Positive seasonal thermal acclimation is observed up to acclimation temperatures of 19.5–20°C, which is also the temperature of minimum respiratory response to all acute test temperatures.
  • 4.4. Regions of thermal metabolic insensitivity are seen over small acute temperature ranges near the acclimation temperatures.
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12.
  • 1.1. Cellular and intracellular localization of catalase and acid phosphomonoesterase in the midgut of Lumbricus terrestris was studied by use of tissue fractionation.
  • 2.2. At least 60–70% of the catalase resides in the chloragocyte cytosol and the remaining 30–40% resides in gut epithelium peroxisomes.
  • 3.3. One of the main functions of the chloragocyte catalase is probably scavenging for H2O2 arising from the interaction between blood heme-protein and oxygen.
  • 4.4. A simple method for the histochemical detection of cytosol catalase is proposed.
  • 5.5. About 10% of the gut acid phosphatase resides in chloragocyte lysosomes. The chloragosomes contain no acid phosphatase.
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13.
  • 1.1. The oxygen consumption of the marine teleost, Lichia amia was investigated under controlled laboratory conditions.
  • 2.2. The routine oxygen consumption showed a strong circadian rhythm with the fish being mainly active during the light period.
  • 3.3. The specific mass exponent (dimension: μg O2/g/hr) is temperature independent and ranges from 0.27–0.29.
  • 4.4. Starving the fish results in a mean decrease in active, routine and standard oxygen consumption of 21%, 24% and 20%, respectively.
  • 5.5. Feecling led to an increase in the oxygen consumption of the teleosts, with the mean metabolic rate over the 24 hr that followed, being 58% and 50% higher for fish that had been starved for 162hr and 40 hr, respectively.
  • 6.6. Apparent SDA showed some variation and ranged from 6.0 to 35.5%.
  • 7.7. The results obtained are generally in agreement with those recorded for other teleosts.
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14.
  • 1.1. The effect of cold (8 ± 2°C) acclimation on the lactate dehydrogenase activities and isoenzyme patterns from sartorius muscle, liver, heart and brain of adult Discoglossus pictus pictus (Otth.) was studied.
  • 2.2. Two groups of animals were studied: one set of animals was trapped in October and another set in December. In both cases some of the animals were sacrificed upon collection and some others subjected to 5 months of acclimation at 8 ± 2°C before being sacrificed for analysis.
  • 3.3. A general trend towards a decrease in LDH specific activity was observed during cold acclimation. The magnitude of change, but not the direction, depends on both the tissue examined and the season at which the experiment was initiated.
  • 4.4. A complex LDH isoenzyme reorganization was also found in liver, heart and brain. In liver from Experiment 1 and in heart from both experiments, a relative maintenance in M-type LDH activity during cold acclimation was observed. However, in brain there was a relative maintenance of LDH3 activity in both experiments.
  • 5.5. The low behavioral activity (and its metabolic consequences) and the existence of an intrinsic annual rhythm in D. pictus metabolism are suggested as responsible for the observed enzymatic changes.
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15.
  • 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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16.
  • 1.l. High amino acid concentrations were found in the anterior coelomic fluid of a Polychaeta (Sabella pavonina Savigny).
  • 2.2. The concentrations being much higher in the fluid which penetrates the nephrostomia into the nephridia lumen than in the final urine indicates that the nephridia reabsorbs large amounts of amino acids.
  • 3.3. Nephridial perfusion experiments showed that an amino acid analogue (α-amino-iso-butyric acid, AIB) is transported by the nephidia.
  • 4.4. The transport took place across the nephridial wall owing to the presence of a carrier-mediated transport system and a diffusion system.
  • 5.5. For the carrier-mediated transport, the Vmax was 0.234 ± 0.025 nmol·min and the Km 3.715 ± 0.315mmol·l.
  • 6.6. AIB accumulated in the nephridial cells up to a maximum rate of 01.17 nmol·min.
  • 7.7. Intracellular accumulation stopped increasing when the Vmax for reabsorption was reached.
  • 8.8. These results indicate that the carrier-mediated transport of AIB is located at the apical membrane of the nephridial cell, and that AIB transport by simple diffusion takes place through the paracellular pathway.
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17.
  • 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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18.
  • 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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19.
  • 1.1. An alkaline p-nitrophenylphosphate phosphatase has been purified 440-fold from extracts of Hatobacterium halobium.
  • 2.2. The enzyme has an apparent molecular weight of 24,000.
  • 3.3. A Km value for p-nitrophenylphosphate of 1.12mM has been found under optimal conditions.
  • 4.4. The enzyme is selectively activated and stabilized by Mn2+.
  • 5.5. It requires high salt concentrations for stability and maximum activity.
  • 6.6. It displays an unusual restricted substrate specificity of 25 phosphate esters tested, only phosphotyrosine and casein were hydrolysed besides p-nitrophenylphosphate.
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20.
  • 1.1. The pattern of VO2 of 4 and 25°C acclimated Cambarus acuminatus was one of normal compensation with cold acclimation resulting in translation and clockwise rotation of the rate-temperature (R-T) curves.
  • 2.2. Acclimation patterns were significantly influenced by the sequence in which crayfish experienced experimental temperatures.
  • 3.3. Eyestalk extracts prepared from warm acclimated crayfish significantly decreased VO2 in eyestalkless cold acclimated recipients.
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