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1.
  • 1.1. Observation of ventilation in immersed Pholis gunnellus showed a linear relationship between ventilatory rate and temperature between 8 and 20°C.
  • 2.2. At 13°C and after 30 min emersion, ventilatory rate was initially lower than prior to emersion, providing evidence of adequate uptake of O2 for standard metabolism during the emersion period.
  • 3.3. This species has a laterally elongate body form with reduced scales and extensive mucus secretion.
  • 4.4. During emersion, gaping behaviour probably exposes the gills and extensively vascularised oesophageal regions to air.
  • 5.5. These are considered to be morphological and behavioural adaptations by P. gunnellus, to aerial respiration in the intertidal habitats occupied by this species.
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2.
  • 1.1. The pharyngeal movements of Trionyx sinensis during submersion where recorded with physiological instruments.
  • 2.2. Anoxia or hypercapnia caused a marked increase in breathing rate of tested turtles during voluntary diving, and in anoxia there was a significant increase in the frequency of aquatic pharyngeal movements while hypercapnia had a slight or no effect on the frequency of these movements.
  • 3.3. During voluntary diving when turtles could easily extend their heads out of water to breathe air, the frequency of rhythmic pharyngeal movements was lower; but during forced submersion, the frequency was higher and the movements were continuous.
  • 4.4. The frequency increased more rapidly and greatly when turtles were in forced submersion than when they dived freely and could easily surface to breathe in N2.
  • 5.5. The frequency of pharyngeal movements of T. sinensis during diving in an aquarium with water depth of 30 or 45 cm was markedly higher than that at a water depth of 15 cm. Disturbing stimuli also influenced the aquatic rhythmic pharyngeal movements of T. sinensis.
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3.
  • 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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4.
  • 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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5.
  • 1.1. The effect of oxygen tension, po2, on oxygen uptake and tolerance to anoxia have been studied by exposure in nitrogen atmosphere and diving in the water snakes Helicops modestus and Liophis miliaris, at 25°C.
  • 2.2. The critical Po2, was the same (70mmHg O2) for both species, but below that tension H. modestus showed a higher degree of dependence on Po2.
  • 3.3. Anoxia tolerance time was longer (14 min for H. modestus and 4 min for L. miliaris) during forced dive than during exposure to a 100% nitrogen atmosphere. No difference was found in pre- and post-forced dive oxygen uptake values in both species.
  • 4.4. The maximum duration of a voluntary dive was shorter than the mean tolerance time to forced dives in L. miliaris. but longer in H. modestus.
  • 5.5. H. modestus, the more aquatic species, is significantly more tolerant of complete anoxia (100% N2 exposure) and submersion.
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6.
  • 1.1. In 20 cockerels with various degrees of NH4Cl-induced chronic acidosis, we separated the pCO2 affecting intrapulmonary chemoreceptors (IPC) from PaCO2 by ligating the left pulmonary artery, denervating the IPC in the right lung and artificially ventilating each lung separately.
  • 2.2. Increased ventilatory depth and decreased ventilatory frequency resulted from (a) increasing P1CO2 to the innervated non-perfused lung (PIPCCO2) during constant PaCO2, (b) increasing PaCO2 during constant PIPCCO2 and (c) increasing in the degree of chronic acidosis.
  • 3.3. Ventilatory sensitivity to PIPCCO2but not to PaCO2 is decreased by chronic acidosis. This coincides with studies where IPC discharge was measured during chronic acidosis and suggests that the mechanism of IPC control of ventilation differs from those of other chemoreceptors.
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7.
  • 1.1. Both the small riparian skink Sphenomorphus quoyii and its completely terrestrial relative Ctenotus robustus respond to forced submergence with instantaneous bradycardia.
  • 2.2. The strength of the bradycardia was affected by water temperature and fear. Dives into hot (30°C) water produced weak and erratic bradycardia compared to dives into cold (19.5°C) water. For S. quoyii the strongest bradycardia occurred when submergence took place in water at a lower temperature than the pre-dive body temperature.
  • 3.3. Upon emergence both species of skink exhibited elevated heart rates and breathing rates while heating from 19.5 to 30°C, compared to heating at rest. The increased heart and breathing rates probably act to replenish depleted oxygen stores and remove any lactate. Increased heart and ventilation rates are not indicators of physiological thermoregulation in this case.
  • 4.4. Both lizard species exhibited higher heart rates and ventilation frequencies during heating than cooling.
  • 5.5. Compared to its terrestrial relative, S. quoyii does not appear to possess any major thermoregulatory, ventilatory or cardiovascular adaptations to diving. However, very small reptiles may be generally preadapted to use the water to avoid predators.
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8.
  • 1.1. Fructose 2,6 P2 and PFK-2 have a key role in the regulation of glycolysis-gluconeogenesis in fish
  • 2.2. PFK-1 and FBPase-1, as in mammals, are the target enzymes for fructose 2,6 P2, this in turn may be controlled by glucagon and insulin.
  • 3.3. PFK-2 from fish liver seems to be a bifunctional enzyme regulated by phosphorylation/dephosphorylation.
  • 4.4. Starvation, refeeding, diet composition and anoxia studies provide a general view of the fructose 2,6 P2 fish system from which the differences between fish and mammal glycolysis-gluconeogenesis may be ascertained.
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9.
  • 1.1. At 35°C a maximal VO2 value of 110 ml O2/kg/hr was obtained with a significant decrease in the value at 40°C.
  • 2.2. The Bohr-effect for P. warreni is — 0.28 and does not change significantly at 15, 25 and 35°C.
  • 3.3. The ability of the crab to extract oxygen from the water medium during a single exhalation is on average 41.2% whilst the limitation diffusion (L. diff, Piiper, [1982], A Companion to Animal Physiology, pp. 49–64. Cambridge University Press.) is 0.84.
  • 4.4. Compared to land and marine crabs, in P. warreni, the PaO2 (29.5 mm Hg) and the PvO2 (15.3 mm Hg) is low.
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10.
  • 1. The two hemoglobins, Hb I and II, of the obligate air-breathing catfish,Hoplosternum littorale have been isolated.
  • 2. The unfractionated stripped hemoglobin has a high oxygen affinity, a normal alkaline Bohr effect, and a Root effect.
  • 3. Both the Bohr and Root effects are enhanced by 1 mM ATP.
  • 4. Stripped Hb I has a relatively high oxygen affinity, a reversed Bohr effect between pH 6.0 and 8.0 (Δlog P502DpH> 0), but no Root effect. Addition of 1 mM ATP to Hb I causes a marked reduction in the oxygen affinity, a change to a normal alkaline Bohr effect (Δlog P50ΔpH< 0), but no Root effect.
  • 5. Stripped Hb II has a lower oxygen affinity at low pH and a higher oxygen affinity at high pH than does Hb I. Hb II shows a large alkaline Bohr effect which is only slightly increased by 1 mM ATP and a Root effect at low pH which is enhanced by 1 mM ATP.
  • 6. The observed rates of O2 dissociation and of CO combination with Hbs I and II show differences which parallel those observed in the oxygen equilibrium measurements.
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11.
  • 1.1. The properties of ATPase activity were studied with the cells at the early stationary phase of Saccharomycopsis fibuligera.
  • 2.2. Optimal pH for the activity was approximately 7.
  • 3.3. The activity was stimulated by Mg2+.
  • 4.4. The activity was inhibited by NaF, DCCD, oligomycin, NaN3, NaVO3, or PCMB but not inhibited by ouabain.
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12.
  • 1.1. Carp (Cyprinus carpio) were stressed to exercise by rolling in a respiration chamber. Ventilatory water flow rate, cardiac output and blood respiratory parameters were determined.
  • 2.2. During exercise, oxygen uptake increased about 3.5-fold and returned to pre-exercise level within 15 min.
  • 3.3. This exercise-stress resulted in no plasma acidosis and in no swelling of the erythrocytes.
  • 4.4. Ventilatory water flow rate increased 6-fold, whereas cardiac output increased 2-fold. Hence the ventilation-perfusion ratio increased during exercise.
  • 5.5. During exercise, arterial O2 content (CaO2) increased due to increases in O2 tension (PaO2), O2 saturation of hemoglobin (SaO2) and hemoglobin concentration (Hb). On the other hand, Pv̄O2 and Sv̄O2 remained at the resting levels but Cv̄O2 slightly increased due to an increase in Hb.
  • 6.6. Arterial-venous O2 difference (CaO2-Cv̄O2) increased by 38%, which was met by a much greater increase in CaO2 than Cv̄O2.
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13.
  • 1. Respiratory properties of piranha blood are distinguished from those of other fish primarily by the high CO2 buffering capacity (ΔHCO3/ΔpH= 19.6mmol/l for oxygenated blood and 39.1 mmol/l for deoxygenated blood).
  • 2. The concentration of nucleoside triphosphates (NTP) and the half-saturation tension (P50) of whole blood were found to be inversely related to body size.
  • 3. The higherP50 in smaller fish, analogous to values obtained in previous studies involving interspecies comparisons, could be adaptive to a higher weight-specific metabolic rate.
  • 4. Both ATP and guanosine triphosphate (GTP) lowered the oxygen affinity of purified hemoglobin solutions, accounting for the size-dependent correlation ofP50 and NTP concentration in whole blood.
  • 5. While similar in concentration in red cells, GTP is more potent than ATP as an allosteric modifier of hemoglobin function.
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14.
  • 1.1. Indian River male broiler chickens growing from 7 to 28 days of age were fed diets containing 12, 18, 24 and 30% protein + 0 or 1 mg triiodothyronine (T3)/kg of diet to study energetic costs of lipogenesis and the use of various substrates for in vitro lipogenesis.
  • 2.2. De novo lipid and CO2 production were determined in the presence of [1-14C]pyruvate, [2-14q]pyruvate, [3-14C]pyruvate, [2-14C]acetate and [U-14C]alanine.
  • 3.3. Oxygen consumption was determined in mitochondrial preparations to estimate the energetic costs in expiants synthesizing lipid.
  • 4.4. Radiolabeled CO2 derived from [1-14C]pyruvate was used as an estimate of coenzyme A availability in liver expiants. Lipids derived from [2-14C]pyruvate, [2-14C]acetate and [U-14C]alanine estimate relative substrate efficiency.
  • 5.5. Labeled CO2 production from [1-14C]pyruvate was greatest in that group fed a 12% protein diet and least in the group fed a 30% protein diet.
  • 6.6. In addition, T3 increased CO2 production from [1-14C]pyruvate.
  • 7.7. The production of 14CO2 from the second carbon of pyruvate or acetate was increased by T3.
  • 8.8. The low-protein diet (12% protein) increased (P <0.05) lipogenesis.
  • 9.9. Adding T3 to the diets decreased carbon flux into lipid from all substrates, but increased CO2 production from all substrates without changing stage 3 and 4 respiration rates in mitochondrial preparations.
  • 10.10. These observations imply that coenzyme A availability may have regulated de novo lipogenesis in the present study.
  • 11.11. It was also concluded that previously noted effects of T3 on intermediary metabolism may involve metabolic pathways that do not involve changes in mitochondrial function.
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15.
  • 1. The whole blood of the non-air-breathing gymnotid teleost,Sternopygus macrurus, is half-saturated with oxygen at 5.2 mm Hg (apparent value) at 30°C in the absence of CO2. Addition of 5.6% CO2 causes the apparentP50 value to increase over 3-fold.
  • 2. The oxygen affinity of the stripped single-component hemoglobin at 20°C increases about 20-fold between pH 5.8 and 8.6 in the absence of ATP. This difference increases to 100-fold in the presence of 1 mM ATP.
  • 3. A substantial Root effect is present: the stripped hemoglobin is only 70% saturated with O2 at pH less than 6 when equilibrated with air.
  • 4. The value of the Hill coefficient,n, is maximal near pH 7.0–7.5, and approaches 1.0 at high pH. The value is about 1.5 at low pH in the absence of ATP and 1.0 in the presence of 1 mM ATP.
  • 5. The O2 dissociation kinetics are heterogeneous at all pH values but most heterogeneous at low pH. The rate increases substantially as the pH decreases.
  • 6. The CO combination kinetics as measured by the stopped flow technique are largely homogeneous except at high pH, but the CO combination kinetics after flash photolysis are markedly heterogeneous.
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16.
  • 1.1. Changes in glomerular nitration rate (GFR), urine and blood properties and plasma catecholamines of carp were investigated during and following hypoxia.
  • 2.2. GFR and urine flow decreased with increased urinary concentrations of bio-components, except protein, in the course of hypoxia.
  • 3.3. Decreases in blood pH, and increases in haematocrit value and plasma K+, Ca2+, Mg2+, inorganic phosphate (Pi), ammonia, lactic acid and catecholamines (CAs) were observed as hypoxia progressed.
  • 4.4. Increased GFR and urine flow, and higher values for urinary components, except protein, compared with those of the control were found in the initial post-stress stage.
  • 5.5. The possible significance of increased plasma CAs in relation to changes in renal function in hypoxic carp is discussed.
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17.
  • 1.1. Insulin stimulated intracellular accumulation of α-amino-isobutyric acid (AIB) in kidney cortex slices from young lambs and piglets.
  • 2.2. The effect was similar in the absence or presence of glucose.
  • 3.3. The induction of the stimulatory effect on renal AIB transport was blocked by cycloheximide. an inhibitor of protein synthesis.
  • 4.4. The insulin stimulation of intracellular AIB accumulation is due to an increased influx and not to a reduced efflux of AIB.
  • 5.5. Analysis of transport kinetics for AIB showed that insulin increased Vmax but did not change Km.
  • 6.6. It is concluded that insulin stimulates uptake of certain neutral amino acids into kidney cortex cells in young animals.
  • 7.7. The effect on renal amino acid transport appears to be mediated through increased synthesis of a membrane carrier.
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18.
  • 1.1. The hemoglobin of Paramecium caudatum has been purified to a state of homogeniety on polyacrylamide disc electrophoresis.
  • 2.2. The hemoglobin appears as a single molecular species with a mol. wt of 13,500 daltons as determined by SDS disc electrophoresis.
  • 3.3. An isoelectric point of 4.27 was calculated from isoelectric focusing experiments using ampholines in a pH range of 3–6.
  • 4.4. The amino acid composition is: lys5, his2, arg3, asp12, thr11, ser9, glu16, pro2, gly18, ala21, cys0, val12, met2, ile2, leu8, tyr2, phe6.
  • 5.5. The spectra of three ferrous and the ferric cyanmethemoglobin derivatives are presented.
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19.
  • 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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20.
  • 1.1. DEAE-cellulose chromatography of mycelial alkaline phosphatase (orthophosphoric monoester phosphohydrolase, EC 3.1.3.1) from Basidiobolus haptosporosus, produced three iso-enzymes “A”, “B” and “C”.
  • 2.2. Fraction “A” was further characterized and showed maximum activity at pH 10 in 0.1 M sodium carbonate-bicarbonate buffer.
  • 3.3. The enzyme was stimulated by Mg2+, Co2+ and Mn2+ and inactivated by Zn2+, Cu2+, EDTA, citrate and tartrate.
  • 4.4. Phosphate ions inhibited it competitively, phenylalanine uncompetitively and urea noncompetitively.
  • 5.5. It was heat stable for 60 min at 37°C but labile above 55°C.
  • 6.6. Its Km with p-nitrophenylphosphate was 0.5 mM; its estimated molecular weight was 160,000.
  • 7.7. The results are compared with the properties of alkaline phosphatases from the rainbow lizard and man and discussed in terms of a triadic association between the fungus, the lizard and man.
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