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1.
  • 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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2.
3.
  • 1.1. Membrane-bound (Na+ + K+)-ATPase activity from the non-innervated and innervated faces of Electrophorus electricus (L.) electric organ, obtained by differential centrifugation, was measured using AChE as an enzyme marker for membranes derived from the post-synaptic area (fraction P3) of the electrolyte.
  • 2.2. The effect of Li+ and Ba2+ on (Na+ + K+)-ATPase activity of the two membrane fractions (P2 and P3) was analysed with respect to K+ and Mg2+ ions, after the I50 estimation.
  • 3.3. The kinetics of the reactions with these cations were investigated showing that Li+ inhibits P2 uncompetitively and for P3 presented a mixed type inhibition.
  • 4.4. Ba2+ behaved as an hyperbolic mixed type inhibitor for P2 and a linear mixed type inhibitor for P3 fraction.
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4.
Methane formation from H2/CO2 by methanogenic bacteria is dependent on Na+ ions. In this communication it is shown with Methanobacterium thermoautotrophicum that a Na+/H+ antiporter plays a role in methane formation from H2 and CO2 and in the regulation of the ΔpH. This is based on the following findings:
  1. Li+ ions, an alternative substrate of Na+/H+ antiporters, could replace Na+ in stimulating methanogenesis from H2 and CO2.
  2. Harmaline, amiloride, and NH 4 + , which are inhibitors of Na+/H+ antiporters, inhibited methanogenesis; inhibition was competitive to Na+ or Li+.
  3. Addition of Na+ or Li+ rather than of other cations to cell suspensions resulted in an acidification of the suspension medium. The rate and extent of acidification was affected by those inhibitors, which inhibited methanogenesis competitively to Na+ or Li.
  4. During methane formation from H2 and CO2 the generation of a ΔpH (inside alkaline) was dependent on the presence of Na+ or Li+. However, methanogenesis was also dependent on Na+ or Li+ under conditions where ΔpH was zero.
  5. ATP synthesis driven by an electrogenic potassium efflux was significantly enhanced in the presence of Na+ or Li+. Na+ or Li+ were shown to prevent acidification of the cytoplasm under these conditions.
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5.
  • 1.1. The properties of Na+/K+-transporting ATPase in microsomal fractions from the nervous tissue of the grasshopper, Poekilocerus bufonius were investigated.
  • 2.2. Two components of ATPase activity are present.
  • 3.3. Inclusion of 1 mM ouabain in the incubation media reduced the activity of total and Na+/K+-ATPase by 57 and 79%, respectively.
  • 4.4. The maximum velocity (Vmax) was decreased by the addition of 1 mM ouabain, whereas the apparent Km value was not affected indicating a non-competitive type of inhibition.
  • 5.5. The calculated value of the pI50 was 6.4 (I50 = 3.98 × 10−7M) for ouabain inhibition of the enzyme showing great sensitivity to the cardiac glycoside ouabain.
  • 6.6. The present results show that the physicochemical properties of Na+/K+-transporting ATPase from the brain of P. bufonius are essentially the same as for the enzyme prepared from the excretory system of the insect which has been previously investigated.
  • 7.7. Dissimilarities were also observed between these tissues in the way that the enzyme from the brain was sensitive to ouabain inhibition with a non-competitive type rather than a ouabain-resistance and a competitive type of inhibition for the enzyme from the excretory system.
  • 8.8. These dissimilarities are probably due to different isoenzyme patterns available in the same insect.
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6.
  • 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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7.
  • 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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8.
  • 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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9.
  • 1.1. The (Na+ + K+)- and Na+-ATPases, both present in kidney microsomes of Sparus auratus L., have different activities and optimal assay conditions as, in the first of the two stocks of fish used (A), the spec. act. of the former is 51.7 μmol Pi mg prot−1 hr−1 at pH 7.5, 100 mM Na+, 10 mM K+, 17.5 mM Mg2+, 7.5 mM ATP and that of the latter is 6.5 μmol Pi mg prot−1 hr−1 at pH 6.5, 40 mM Na+, 4.0 mM Mg2+, 2.5 mM ATP.
  • 2.2. Ouabain and vanadate specifically inhibit the (Na+ + K+)-ATPase but not the Na+-ATPase that is preferentially inhibited by ethacrynic acid.
  • 3.3. While the (Na+ + K+)-ATPase is strictly specific for ATP and Na+, Na+-ATPase can be activated by various monovalent cations and, apart from ATP, hydrolyses CTP, though less efficiently.
  • 4.4. The second stock B, subjected to higher salinity than A, shows an acidic shifted Na+-ATPase optimal pH, opposed to the stability of that of the (Na+ + K+)-ATPase, a decreased (Na+ + K+)-ATPase and a strikingly depressed Na+-ATPase.
  • 5.5. The results are compared with literature data and discussed on the basis of the presumptive different roles as well as functional prevalence in various salinities of the two ATPases.
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10.
  • 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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11.
  • 1.1. Na/H exchange is the major pathway for Na uptake in brush border membrane vesicles from chicken small intestine. Hanes-Woolf analysis demonstrated that Na and H competed at the same extravesicular site. The KNa for Na+ at extravesicular pH 6.6 is 35 mM and at pH 7.4, 12 mM.
  • 2.2. Similar to mammalian intestinal cells, the Na/H exchanger does not appear to have an internal proton modifier site. Varying intravesicular pH from 6.1 to 7.8 stimulates uptake, but a sigmoidal relationship is not observed.
  • 3.3. The ability of several amiloride analogs to inhibit the exchanger was tested and the inhibitory profile was similar, but not identical to Na/H exchangers in mammalian tissues. The potency series (from most to least potent) is hexamethylamiloride ≈ ethylisopropylamiloride > methylisobutylamiloride > dimethyl-amiloride > amiloride.
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12.
  • 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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13.
  • 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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14.
  • 1.1. The influx and transepithelial movements of l-methionine and its effects on the electrophysiology and Na-Cl-transport in upper and lower intestine of the cultured fish, Spanis aurata, were measured.
  • 2.2. The Km and Vmax of l-methionine influx into the tissues were higher in lower intestine than in upper intestine. A prominent diffusion-like transport component was also measured in both segments during influx experiments.
  • 3.3. Net transepithelial fluxes of l-methionine (1 mM) were observed in both upper and lower intestine, this transport being Na+-dependent.
  • 4.4. The two intestinal segments exhibited an electrical potential difference (PD) and a short circuit current (Isc) serosa negative or near zero. Tissue conductance (Gt) was higher in posterior than in lower intestine.
  • 5.5. Addition of l-methionine to the mucosal side of lower or upper intestine did not induce changes in PD in either part.
  • 6.6. Isotopic fluxes of Cl or Na+ measurements under short circuit conditions showed that there were no net Cl or Na+ transport in either part.
  • 7.7. l-Methionine additions to the mucosa did not induce changes in unidirectional fluxes of Cl or Na+ or in the (Isc) in either the anterior or posterior intestine.
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15.
  • 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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16.
  • 1.1. Uptake of l-leucine, l-phenylalanine, l-proline and l-lysine into brush border membrane vesicles from rats fed either a medium-chain triglyceride (MCT) or a long-chain triglyceride (LCT) diet was studied under conditions of the presence or absence of a Na+ gradient.
  • 2.2. From the results of initial rate, Na+-dependent transport in LCT feeding were lower than in feeding MCT. The Na+-independent transport did not vary in either group except for l-lysine uptake.
  • 3.3. For l-leucine, l-phenylalanine and l-proline in Na+ dependence, kinetic analysis revealed 4–6-fold smaller Vmax values in LCT group than in MCT group. l-Lysine in Na+-independent transport was 10-fold lower in LCT group than in MCT group. The Km values were not affected by feeding the LCT or MCT diet.
  • 4.4. It is clear that amino acid transport is regulated by different types of dietary fat. We consider that the alteration of transport activity is attributable to the changes in number of membrane-bound transport carriers but not to their affinity.
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17.
  • 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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18.
  • 1.1. The shell side of the mantle of Achatina fulica is several millivolts positive to the blood side in vitro.
  • 2.2. The electrical potential does not depend on Na+, Ca2+, Mg2+, K+ or HCO3 but requires the presence of chloride on the shell side.
  • 3.3. The potential difference and short-circuit current ranged from 3.0 to 30.0 mV and 15.0 to 75 μA/cm2 with averages at 10m V and 50 μA/cm2 respectively.
  • 4.4. The electrical gradient is reduced by 2,4-dinitrophenol, thiocyanate and furosemide but not by ouabain, CO2 or acetozolamide.
  • 5.5. It is suggested that the nature and mechanism of electrogenesis in Achatina parallels that of the Helix mantle.
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19.
  • 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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20.
  • 1.1. After ionic composition of superficial fluid (ISF) and interstitial fluid (ISF) of the frog Rana catesbeiana) tongue had mostly been changed with a low Na+ saline solution, the relations between membrane potentials and receptor potentials in a frog taste cell evoked by various concentrations of NaCl and various types of salts were analyzed to examine permeability of the taste receptive membrane to cations and anions.
  • 2.2. The mean reversal potentials for depolarizing potentials of a taste cell in response to 0.05 M, 0.2 M and 0.5 M Nad were -40.0, 6.4 and 28.8 mV, respectively.
  • 3.3. When adding an anion channel blocker, SITS, to a NaCl solution the reversal potential for receptor potential with NaCl plus SITS became about twice as large than with NaCl alone.
  • 4.4. Reversal potentials for 0.2 M NaCl, LiCl, KCl and NaSCN were 6.4, 25.4, −1.0 and −7.8 mV, respectively, indicating that permeability of the apical taste receptive membrane to cations of Cl salts is arranged in the order of Li+ > Na+ > K+ and that the permeability to anions of Na+ salts is arranged as SCN > Cl
  • 5.5. It is concluded that in the case of NaCl stimulation, Na+ and Cl of NaCl stimulus permeate NaCl-gated cationic and anionic channels at the apical taste receptive membrane in generating receptor potentials.
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