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1.
  • 1.1. The ventricle cells of the flounder (Platichthys flesus) maintained the cell volume regulation mechanism in vitro, when isolated hearts were submitted to a hyposmotic solution.
  • 2.2. The initial osmotic swelling of the cells was followed by a secondary shrinking. A new steady state volume (water content) was established in the course of 6 hr. The water content was 3% above control.
  • 3.3. The cellular amount of K+ and taurine decreased concomitantly with the decline in cellular water.
  • 4.4. The decrement in cellular taurine was explained by leakage of taurine, per se, into the perfusion media.
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2.
  • 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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3.
  • 1.1. Weekly injections of bovine growth hormone (bGH) increased the maximal transport rate of both Na+-dependent and Na+ -independent l-leucine transport with little effect on the affinity constants in the intestine of striped bass hybrids.
  • 2.2. The Na+-dependent and the Na+-independent transport of the non-metabolizable analog cycloleucine was also stimulated by bGH.
  • 3.3. The Na+ -dependent active transport was stimulated 2 days after the hormone treatment, while the stimulation of the Na+-independent diffusional transport was not observed until after 2 weeks of treatment.
  • 4.4. Studies of intestinal morphometry and l-leucine transport using brush border membrane vesicles suggested that bGH affects intestinal amino acid absorption initially by increasing the number of transporters per cell.
  • 5.5. This phase is followed by a general increase of the intestinal mass after long-term treatment with the hormone.
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4.
  • 1.1. Mineral balance was studied in meadow voles (Microtus pennsylvanicus) maintained in the laboratory.
  • 2.2. Urine and fecal Na+ contents of voles on low-Na+ diets were comparable to those reported for other herbivore species, but urine and fecal K levels were higher.
  • 3.3. Voles approached Na+ balance (input = output) on diets with Na+ content as low as 56 ppm.
  • 4.4. There was not a clearcut hypertrophy of the adrenal-gland zona glomerulosa in voles maintained on low-Na+ diets.
  • 5.5. Plasma K content and bone water content were higher in voles maintained on high-Na + vegetation diets, suggesting expansion of extracellular fluid volume.
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5.
  • 1.1. In brush border membrane vesicles isolated from eel kidneys, adapted either to sea water or freshwater environments, a Na+/H+ antiporter is present.
  • 2.2. Using a calibration plot it is possible to evaluate the amount of protons that this antiporter can accumulate inside the vesicular space.
  • 3.3. The activity of the antiporter seems to be affected by the salinity of the water; it is higher in animals adapted to seawater.
  • 4.4. This adaptation seems to occur by a Jmax regulation of the antiporter.
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6.
  • 1.1. Specific activity and kinetic characteristics of the (Na+ + K+)ATPase have been investigated in the gill epithelium of the hyper-hypoosmoregulator crab Uca minax.
  • 2.2. (Na+ +K+)ATPase activity is shown to be at least three times higher in the posterior gills.
  • 3.3. The kinetic study supports the hypothesis of the existence of two different (Na+ + K+)ATPases: the enzyme activity in the posterior gills could be involved in the transepithelial transport of Na+ while the activity of the anterior gills could be responsible for the intracellular regulation of Na+ and K+.
  • 4.4. Significant and specific changes in (Na+ +K+)ATPase activity occur upon acclimation to media of various salinities.
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7.
  • 1.1. Nicotine at 10 mM, but not caffeine or theophylline, reduced by 20% the overshoot of the Na+-dependent d-glucose transport in ratjejunal brush border membrane vesicles.
  • 2.2. Since nicotine did not affect the transport of Na+, its inhibition on Na+-dependent d-glucose transport must be due to a direct effect upon the d-glucose transport system.
  • 3.3. Folate transport in these membrane vesicles was found to a be a free diffusion process at pH 7.4.
  • 4.4. Neither caffeine, theophylline nor nicotine has any effect on folate transport.
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8.
  • 1.1. Unidirectional Na+ influx in lamprey red blood cells was determined using 22Na as a tracer.
  • 2.2. Total Na+ uptake and amiloride-inhibitable Na+ influx increased in a saturable fashion as a function of external Na+ concentration (Nae).
  • 3.3. At 141 mM Nae, the average value of net Na+ influx was 13 ± 1.1 and the amiloride-sensitive Na+ influx was 5.3±1.1 mmol/l cells per hr (±SE).
  • 4.4. The amiloride-sensitive component of Na+ influx was significantly activated by 10−5 M isoproterenol, by 2 × 10−5 M DNP, and by cell shrinkage.
  • 5.5. Furosemide (1 mM) had no effect on the Na+ transport in red cells.
  • 6.6. The residual amiloride-insensitive component of Na+ transport was a linear function of Nae in the range of 5–141 mM. This transport seems to be accounted for by simple diffusion.
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9.
  • 1.1. Activities of Na+-K+ ATPase and carbonic anhydrase were measured through the early post-embryonic development of Penaeusjaponicus. In adults, only the Na+-K+ ATPase activity was measured.
  • 2.2. ATPase activity was variable in the successive development stages. From zero in nauplii, the activity slightly increased in zoeae, and rose sharply in mysis stages 2 and 3.
  • 3.3. A further significant increase in activity was noted at the transition from late mysis to early postlarvae, concomitant with a change from the larval osmoconforming pattern of osmoregulation to the postlarval and adult hyper-hyporegulating pattern.
  • 4.4. The activity of Na+-K+ ATPase, measured in isolated cephalothorax, increased from PL3 to PL4 to its maximum value in PL5; at this stage, osmoregulatory capacity was fully efficient.
  • 5.5. In young stages of P. japonicus, the variations in Na+-K+ ATPase activity appear correlated with the development of osmoregulatory ultrastructures, and with osmoregulation and salinity tolerance.
  • 6.6. These results are discussed with regard to their ecological and physiological implications.
  • 7.7. In adults, the activity of Na+-K+ ATPase was high in gills and epipodites and no activity was detected in branchiostegites. These results are related to the ultrastructure of these organs.
  • 8.8. The activity of carbonic anhydrase did not change significantly in larval and postlarval stages.
  • 9.9. From these results, it is proposed that the effector sites of osmoregulation are located in branchiostegites, pleurae and epipodites in postlarvae, and in epipodites and mainly in gills in adults.
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10.
  • 1.1. Homogenates of gills from the freshwater shrimp M. amazonicum exhibit the following ATPase activities: (i) a basal, Mg2+-dependent ATPase; (ii) an ouabain-sensitive, Na+ + K+-stimulated ATPase; (iii) an ouabain-insensitive, Na+-stimulated ATPase; and (iv) an ouabain-insensitive, K+-stimulated ATPase.
  • 2.2. K+ suppresses the Na+-stimulated ATPase activity in a mixed-type kind of inhibition, whereas Na+ does not exert any noticeable effect on the K+-stimulated ATPase activity.
  • 3.3. The Na+- and the K+-stimulated ATPase activities are totally inhibited by 5 mM ethacrynic acid in the incubation medium.
  • 4.4. The Na+- and the K+-stimulated ATPase activities are not expressions of the activation of a Ca-ATPase.
  • 5.5. The possible localization and roles of the described ATPases within the gill epithelium are briefly discussed and evaluated.
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11.
  • 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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12.
  • 1.1. The outer layers of the eel intestine were stripped off and the electrical potential difference (PD) and net water flux across the stripped intestine were measured.
  • 2.2. The PD of serosa-negativity in the stripped intestine was 4 times higher than that in the intact one.
  • 3.3. The high serosa-negative potential was dependent on Cl in the fluids, demonstrating the presence of a Cl pump.
  • 4.4. When Na+ transport was inhibited by either replacement of Na+ with other cations or additions of ouabain, the high serosa-negative potential was reduced to zero.
  • 5.5. The results were discussed in relation to Cl pump-Na+ pump coupling and to sea-water adaptation of the eels.
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13.
  • 1.1. Freshwater gammarids from 900–1400 m depths lose Na at 1 atm, 4°C, while related shallow water gammarids are near neutral Na balance.
  • 2.2. Na+ influx rates are similar at 1 atm, 4°C, for abyssal and shallow water gammarids of similar weight.
  • 3.3. Na+ efflux is faster for abyssal gammarids than for comparable shallow water gammarids.
  • 4.4. Compressing abyssal gammarids to 90–140 atm increases Na+ influx rates enough to restore neutral Na balance, while in shallow water crustaceans, compression decreases Na+ influx.
  • 5.5. Na+ influx rates in Baikalian gammarids vary with the 0.55 power of weight.
  • 6.6. The equation Fma × t = 1.3 × W0.55 μEq/hr/animal applies to freshwater crustaceans over the weight range from 0.03 to 35 g.
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14.
  • 1.1. Uptake of [14C]-labelled d-glucose, l-arabinose and d-fructose by intestinal and renal brush border and basolateral membrane vesicles was studied in the absence of Na+ .
  • 2.2. The Na+-independent d-glucose transport system in these membrane vesicles was saturable, sensitive to phloretin, stereospecific and accessible only to d-glucose and d-galactose.
  • 3.3. Na+-independent l-arabinose transport was not saturable even when its concentration was raised to 300 mM and it was insensitive to phloretin.
  • 4.4. Na+-independent d-fructose transport demonstrated saturation kinetics with only renal brush border membrane vesicles, but it was not inhibited by either phloretin or phlorizin.
  • 5.5. These studies indicated that the Na+-independent carrier-mediated d-glucose/d-galactose transport system of intestinal and renal brush border and basolateral membranes is clearly not shared by other monosaccharides.
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15.
  • 1.1. In crayfish, light stimulation of the retinular cells induces a depolarizing receptor potential.
  • 2.2. Experiments were designed to determine the role of Na+ and Ca2+ on receptor potential during dark And light states.
  • 3.3. Depolarization depends on Na+ and Ca2+ availability to the retinular cell.
  • 4.4. Repolarization velocity and response duration depend on extracellular Ca2+ availability.
  • 5.5. Light adaptation increases receptor potential dependence on calcium and sodium ions.
  • 6.6. We analyse these results with respect to other invertebrate photoreceptors.
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16.
  • 1.1. Behavioural observations and haemolymphatic measurements of Na+ K+ and Ca+ were performed in Chasmagnalhus granulata during emersion.
  • 2.2. Activity levels were found to be higher during voluntary emersion periods than when the animals were submerged. A lt50 of 39.45 hr was observed when no access to water was allowed.
  • 3.3. The Na+ and K+ and Ca+ levels increased during aerial exposure. The Na+ and K+ levels were restored prior the end of the experimental period. Mechanisms for such regulation are therefore discussed. The Ca2+ levels, remaining high during emersion, are probably a result of acid-base balance adjustments.
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17.
18.
  • 1.1. The effect of warm acclimation on the cationic concentrations of hibernating Rhagium inquisitor beetles was studied.
  • 2.2. Following warm acclimation, the extracellular concentration of Mg2+ dropped from about 80 to about 50 mM. For Na+ and K+ the extracellular concentration remained constant at about 40 mM. The estimated intracellular concentration of Mg2+ was not affected by the warm acclimation, being about 80 mM in both groups of beetles. The corresponding concentration of Na+ increased from about 20 to about 30 mM, whereas for K+ there was no change, the concentration being about 140mM in both groups of beetles.
  • 3.3. The marked drop in the extracellular concentration of Mg2+ might indicate that Mg2+ is involved in the regulation of the concentration of glycerol, which was reduced to zero during the warm acclimation.
  • 4.4. The estimated equilibrium potentials of the respective ions might indicate that K+ is in electrochemical equilibrium across the cell membranes, whereas Na+ and to a lesser extent Mg2+ are actively transported out of the cells.
  • 5.5. For Na+ there was a high positive equilibrium potential even in the cold acclimated beetles, indicating that Na+ has a high electrochemical potential difference across the cell membranes even at low temperatures. This is in agreement with the observation that hibernating insects are able to perform coorclinated walking immediately after heating to temperatures near zero.
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19.
  • 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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20.
  • 1.1. The taurine content of erythrocytes from 15 avian species contained levels of taurine in the range of 20–70 mmol/kg of hemoglobin, about 100-fold that of mammalian red blood cells.
  • 2.2. This high taurine content did not appear to be related to the nucleation of these cells as nucleated amphibian erythrocytes and human reticulocytes contained low levels.
  • 3.3. The erythrocytes lacked cysteine sulfinic acid decarboxylase, a key enzyme in the synthesis of taurine from cysteine, indicating a probable lack of synthetic capabilities.
  • 4.4. The cells were able to accumulate labeled taurine against a concentration gradient. This uptake was inhibited by β-alanine and was Na+-dependent.
  • 5.5. When incubated in hypotonic medium, the cell volume of pigeon erythrocytes rapidly increased and was followed by a much slower return to normal size. The cell volume reduction was accompanied by a slow efflux of taurine into the medium.
  • 6.6. These data suggest that taurine plays a role in cell volume maintenance and osmotic regulation in avian erythrocytes.
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