The Absorption of Sodium Ions by the Crayfish, Astacus Pallipes Lereboullet

1960 ◽  
Vol 37 (3) ◽  
pp. 534-547
Author(s):  
J. SHAW
Keyword(s):  
Ion Exchange ◽  
Ammonia Excretion ◽  
External Solution ◽  
Sodium Concentration ◽  
Sodium Sulphate ◽  
Sodium Ions ◽  
Hydrogen Ions ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Sodium Chloride Solutions

1. Sodium influx and net sodium uptake have been measured for the crayfish, Astacus pallipes, in solutions of a variety of sodium salts. 2. The nature of the anion has no effect on the sodium influx. 3. Sodium influx is related to the external sodium concentration in the same way whether the anion is chloride or sulphate. 4. The net sodium uptake rate from sodium sulphate is 65-100% of that from sodium chloride solutions. 5. In sodium sulphate solutions the sulphate ion does not penetrate. 6. There is no increase in ammonia excretion during net sodium uptake from sodium sulphate solutions. 7. An analysis of the external solution by conductivity and ion exchange showed that during sodium uptake sodium ions are not exchanged for metallic cations and must be exchanged either for ammonium or hydrogen ions without increasing their normal rate of excretion. 8. Sodium uptake may sometimes exceed ammonia production so that hydrogen-ion exchange may be involved in these cases. 9. The possibility is discussed that sodium ions exchange for either ammonium of hydrogen ions depending on the metabolic activity of the animal.

Sodium Regulation in the Freshwater Mollusc Limnaea Stagnalis (L.) (Gastropoda: Pulmonata)

1970 ◽  
Vol 53 (1) ◽  
pp. 147-163 ◽  
Author(s):  
PETER GREENAWAY
Keyword(s):  
Blood Volume ◽  
Tap Water ◽  
Sodium Concentration ◽  
Sodium Balance ◽  
Uptake Mechanism ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Limnaea Stagnalis ◽  
Total Body ◽  
Sodium Regulation

1. Sodium regulation in normal, sodium-depleted and blood-depleted snails has been investigated. 2. Limnaea stagnalis has a sodium uptake mechanism with a high affinity for sodium ions, near maximum influx occurring in external sodium concentrations of 1.5-2 mM-Na/l and half maximum influx at 0.25 mM-Na/l. 3. L. stagnalis can maintain sodium balance in media containing 0.025 mM-Na/l. Adaptation to this concentration is achieved mainly by an increased rate of sodium uptake and a fall of 37 % in blood sodium concentration, but also by a reduction of the sodium loss rate and a decrease in blood volume. 4. A loss of 23% of total body sodium is necessary to stimulate increased sodium uptake. This loss causes near maximal stimulation of the sodium uptake mechanism. 5. An experimentally induced reduction of blood volume in L. stagnalis increases sodium uptake to three times the normal level. 6. About 40% of sodium influx from artificial tap water containing 0.35 mM-Na/l into normal snails is due to an exchange component. Similar exchange components of sodium influx were also observed in sodium-depleted and blood-depleted snails in the same external sodium concentration.

scholarly journals The Effect of External Sodium and Calcium Concentrations on Sodium Fluxes by Salt-Depleted and Non-Depleted Minnows, Phoxinus Phoxinus (L.)

1987 ◽  
Vol 131 (1) ◽  
pp. 417-425
Author(s):  
W. J. FRAIN
Keyword(s):  
Sodium Concentration ◽  
Uptake Mechanism ◽  
Sodium Influx ◽  
Sodium Efflux ◽  
Sodium Uptake ◽  
Km Value ◽  
Concentration Changes ◽  
The Relationship ◽  
Very High ◽  
External Calcium

The relationship between sodium influx and external sodium concentration in Phoxinus is complex and unusual. In non-depleted fish the relationship is approximately that given by the Michaelis-Menten equation of enzyme kinetics. However, the Km value (a measure of the affinity of the sodium uptake mechanism for sodium) is very high (3mmoll−1), indicating a low affinity of the uptake mechanism for sodium. On sodium depletion, the relationship between sodium influx and external sodium concentration changes to produce a curve which has a stepped appearance, and is unusual in that the maximum influx is not increased above that in non-depleted fish. The overall Km alters very little; however, the Km for the lower part of the curve is very low (0.05 mmoll−1). A model is proposed to explain these results in the form of two sodium uptake mechanisms working in parallel across the gill. The second carrier is only active when the fish is sodium-depleted and kept in low external sodium concentrations. Neither the external sodium concentration nor the external calcium concentration has any direct effect on sodium efflux. However, fish depleted in 1 mmoll−1 calcium have a lower sodium efflux than fish depleted in distilled water. Calcium appears to reduce the permeability of the gill to ions such as sodium. Since calcium has no effect on sodium influx, changes in gill permeability do not involve the sodium influxmechanism.

Sodium Regulation in the Fresh-Water Amphipod, Gammarus Pulex (L.)

1967 ◽  
Vol 46 (3) ◽  
pp. 499-518
Author(s):  
D. W. SUTCLIFFE
Keyword(s):  
Fresh Water ◽  
Body Surface ◽  
Loss Rate ◽  
Sodium Concentration ◽  
The Body ◽  
Uptake Mechanism ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Sodium Loss ◽  
Total Sodium

1. Sodium influx and loss rates in Gammarus pulex were measured at constant temperatures. The sodium loss rate was immediately influenced by a change in temperature, with a Q10 of 1.5 to 2.0 at temperatures between 0.3 and 21.5° C. The sodium influx rate is apparently influenced in the same way. 2. The sodium uptake mechanism in G. pulex from three localities was half-saturated at an external concentration of 0.10-0.15 mM/l. sodium. 3. The total sodium loss rate remained approximately constant in animals acclimatized to the range of external concentrations from 2 to about 0.2 mM/l. sodium. 18% of the sodium was lost in urine with a sodium concentration estimated at 30-50 mM/l. The remainder of the sodium loss was due to diffusion across the body surface. 4. In animals acclimatized to concentrations below about 0.2 mM/l. sodium the sodium loss rate was reduced, due to (a) a lower diffusion rate following a fall in the blood sodium concentration, and (b) the elaboration of a more dilute urine. 5. There was a very close association between changes in the blood sodium concentration, the elaboration of a very dilute urine, and the rate of sodium uptake at the body surface. The results indicate that a fall in the blood sodium concentration leads to simultaneous activation of the sodium uptake mechanisms at the body surface and in the antennary glands. 6. It is estimated that, by producing a dilute urine, total sodium uptake in G. pulex is shared equally between the renal uptake mechanism and the mechanism situated at the body surface. 7. In sea-water media G. pulex drinks and expels fluid from the gut. In a medium slightly hyperosmotic to the normal blood concentration the amount imbibed was equal to the normal rate of urine flow when in fresh water.

The effect of enternal sodium concentration upon sodium fluxes in Chironomus dorsalis (Meig.) and Camptochironomus tentans (Fabr.), and the effect of other ions on sodium influx in C. tentans

1975 ◽  
Vol 62 (1) ◽  
pp. 141-155
Author(s):  
DA Wright
Keyword(s):  
Steady State ◽  
Sodium Concentration ◽  
Fourth Instar ◽  
Half Maximum ◽  
Uptake Mechanism ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Low Concentrations ◽  
Salt Depletion

In comparison with other freshwater animals, the sodium uptake mechanism in fourth instar larvae of both C. tentans and C. dorsalis has a moderate affinity for sodium. In both species half maximum influx (Km) occurs at about 0.57 mM-Na+ and is unaltered by salt depletion. Maximum influx is achieved in steady-state C. tentans at 1.9 mM-Na+, and in steady-state C. dorsalis at 3.0 mM-Na+. Both of these values increase on depletion. Efflux also appears to be saturable at higher external sodium concentrations. In C. tentans, sodium may be transported independently of chloride, although it seems likely that sodium movement is enhanced by chloride. Sulphate strongly inhibits sodium influx. Nitrate apparently inhibits sodium influx at low concentrations, but this inhibition is progressively overcome at external sodium concentrations approaching 4 mM. A number of cations interfere with sodium influx in depleted C. tentans, notably H+, Li+ and, to a lesser extent NH4+. It is suggested that these ions compete with sodium for carrier sites. Potassium is apparently transported independently of sodium.

The Effect of Some Anions and Cations Upon the Fluxes and Net Uptake of Sodium in the Larva of Aedes Aegypti (L)

1965 ◽  
Vol 42 (1) ◽  
pp. 29-43 ◽  
Author(s):  
R. H. STOBBART
Keyword(s):  
Sodium Concentration ◽  
Sodium Content ◽  
Deionized Water ◽  
Sodium Balance ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Chloride Uptake ◽  
Net Uptake ◽  
The Relationship ◽  
Anal Papillae

1. Starved 4th-instar larvae of Aädes aegypti, when put into deionized water at a density of ten larvae/20 ml., are able to achieve sodium balance at the low external concentration of 5µM Na/l. 2. The balancing process involves a 10% drop in total sodium content, a more or less complete activation of the mechanism for sodium transport, and a reduction in the permeability of the larva to sodium as measured by the net sodium loss into deionized water. It is very probable that most of this reduction occurs in the anal papillae. 3. The relationship between external sodium concentration and sodium influx in larvae previously ‘balanced’ in deionized water is described approximately by the Michaelis equation. The sodium outflux also increases with increasing external sodium concentrations. 4. The net uptake of sodium by ‘balanced larvae’ appears to be significantly greater from solutions of NaCl than from solutions of NaNO3 NaHCO3 and Na2SO4. 5. The ions K+ Ca++ Mg++ and NH4+ when present as chlorides stimulate the influx of sodium from 0.1 mM/l. sodium chloride. When present as nitrates or sulphates they either have no effect or cause an inhibition of influx. 6. The results in 4 and 5 suggest that movements of chloride may be important in sodium uptake, and chloride uptake has been found to occur independently of sodium uptake. Measurements of potential difference between haemolymph and medium demonstrate active transport of both sodium and chloride.

The Absorption of Sodium Ions by the Crayfish, Astacus Pallipes Lereboullet

1959 ◽  
Vol 36 (1) ◽  
pp. 126-144 ◽  
Author(s):  
J. SHAW
Keyword(s):  
Uptake Rate ◽  
Equilibrium Concentration ◽  
Maximum Level ◽  
Sodium Concentration ◽  
Sodium Content ◽  
Sodium Balance ◽  
Sodium Ions ◽  
External Concentration ◽  
Sodium Influx ◽  
True Measure

1. The effects of external and internal sodium concentrations on the uptake of sodium ions by the crayfish, Astacus pallipes, has been studied. 2. The normal sodium influx, measured with 24Na, from O.3 mM /l. NaCl solution is 1.5 µM./10 g. body weight/hr. The rate of loss of sodium to de-ionized water has roughly the same value. 3. Net loss of sodium reduces the external sodium concentration required for sodium balance. The minimum equilibrium concentration is about 0.04 mM./l. NaCl. 4. The relation between the external sodium concentration and the sodium influx is non-linear. The influx has a maximum of about 10 µM./10 g./hr. at an external concentration of approx. 1 mM./l. 5. The 24Na influx is a true measure of the sodium uptake rate at low external concentrations. At higher concentrations the influx may exceed the uptake rate by some 20%. 6. Net loss of sodium increases the influx by three to five times. Loss of 5-10% of the total internal sodium increases the influx from the normal to the maximum level. A 1% change has a significant effect on the influx. Changes in the internal sodium content reflect changes of the blood sodium concentration. 7. A scheme is suggested whereby the external and internal sodium concentrations interact together on the influx to produce a self-regulating system which maintains the animal in sodium balance.

Sodium Influx and Loss in Freshwater and Brackish-Water Populations of the Amphipod Gammarus Duebeni Lilljeborg

1971 ◽  
Vol 54 (1) ◽  
pp. 255-268
Author(s):  
D. W. SUTCLIFFE
Keyword(s):  
Body Surface ◽  
Brackish Water ◽  
Sea Water ◽  
Sodium Concentration ◽  
The Body ◽  
Experimental Population ◽  
Sodium Ions ◽  
Sodium Influx ◽  
Wide Range ◽  
Freshwater Habitats

1. Sodium influx was examined in Gammarus duebeni from freshwater habitats on the Kintyre and Stranraer peninsulas in western Britain, and from a brackish-water habitat in Ireland. The affinity for sodium ions in the uptake mechanism at the body surface was similar in animals from the three localities. 2. Compared with the parent population from Kintyre, an experimental population established for 2 years in water with a lower sodium concentration showed an increased affinity for sodium. 3. Sodium losses in the urine of animals from the above localities were negligible at external salinities below about 2% sea water. In contrast, urinary sodium losses in animals from a brackish-water population in Britain were higher at salinities ranging from 40% sea water to well below 2% sea water. 4. The affinity for sodium ions in uptake mechanisms at the body surface and in the antennary glands of G. duebeni from a wide range of habitats shows a market correlation with the sodium concentration of the habitat. The permeability of the body surface to outward movement of sodium is similar in G. duebeni from brackishwater and freshwater habitats. 5. It is suggested that most of the observed physiological differences between populations of G. duebeni are phenotypic in origin. The status of the freshwater ‘race’ in Ireland is briefly discussed.

scholarly journals Nonelectrolyte Penetration and Sodium Fluxes through the Axolemma of Resting and Stimulated Medium Sized Axons of the Squid Doryteuthis plei

1966 ◽  
Vol 50 (1) ◽  
pp. 43-59 ◽  
Author(s):  
Raimundo Villegas ◽  
Gloria M. Villegas ◽  
Margarita Blei ◽  
Francisco C. Herrera ◽  
Jorge Villegas
Keyword(s):  
Sodium Concentration ◽  
Ionic Species ◽  
The Other ◽  
Sodium Ions ◽  
Drag Effect ◽  
Sodium Influx ◽  
Low Sodium ◽  
External Potassium ◽  
Independent Effects ◽  
Extracellular Sodium

The penetration of 14C-labeled erythritol, mannitol, and sucrose through the axolemma was determined in medium sized paired axons, one at rest and the other stimulated 25 times per sec. The resting permeabilities, in 10-7 cm/sec, are erythritol, 2.9 ± 0.3 (mean ± SEM); mannitol, 2.3 ± 0.4; and sucrose 0.9 ± 0.1. In the stimulated axons they are: erythritol, 5.2 ± 0.3; mannitol, 4.0 ± 0.5; and sucrose, 1.8 ± 0.3. Thus, the calculated permeabilities during activity (1 msec per impulse), in the same units, are: 100, 75, and 38, respectively. These changes in permeability are reversible. The effects of external potassium and sodium concentrations on erythritol penetration were also studied. At rest, erythritol penetration is independent of potassium and sodium concentrations. In the stimulated axons, erythritol penetration decreases when the extracellular sodium is diminished. Sodium influx (not the efflux) decreases during rest and activity when the extracellular sodium is diminished. The diminution during activity of erythritol and sodium entries in low sodium solutions may be related to a decrease of a drag effect of sodium ions on the nonelectrolyte molecules or to independent effects of the sodium concentration on sodium influx and the nonelectrolyte pathways. The axolemma discriminates among erythritol, mannitol, sucrose, and the different ionic species during rest and activity.

Branchial Sodium Transport Mechanisms in Scyliorhinus Canicula: Evidence for Na+/NH4+ and Na+ H+ Exchanges and for A Role of Carbonic Anhydrase

1973 ◽  
Vol 58 (2) ◽  
pp. 487-502
Author(s):  
P. PAYAN
Keyword(s):  
Sodium Transport ◽  
Ammonia Excretion ◽  
Inhibitory Effect ◽  
The Body ◽  
Control Fish ◽  
Transport Mechanisms ◽  
Sodium Influx ◽  
Sodium Efflux ◽  
Sodium Uptake ◽  
Scyliorhinus Canicula

1. Branchial sodium exchanges were measured with the help of 24Na in the marine elasmobranch Scyliorhinus canicula. Handling causes a transient increase of the sodium influx and decrease of the sodium efflux in both intact and hypophysectomized fish. 2. Ammonia-loading (300 µ-equiv./100 g) is followed by an increase of both influx and efflux of sodium resulting in an augmented net sodium uptake lasting for at least 4 h. Ammonia excretion is also increased but only for 2 h. Ammonia-loading results in a metabolic acidosis lasting for at least 4 h. 3. HCl injection (100 µ-equiv./100 g) produces an increase of both influx and efflux of sodium resulting in an augmented net sodium uptake lasting for at least 4 h. Ammonia excretion is not affected. 4. Acetazolamide injection (10 mg/100 g) results in a depression of the sodium influx, while the sodium efflux remains unchanged. This inhibitory effect is observed in control fish as well as in fish treated with HCl or ammonium salt injections. 5. These observations confirm that the gill plays a major role in the maintenance of the pH of the body fluids. The similarities between the sodium transport mechanisms of Scyliorhinus and of the freshwater teleosts are emphasized. These results suggest that living elasmobranchs may have retained branchial mechanisms inherited from their freshwater ancestors.

Kinetics of sodium uptake in freshwater animals: a comparison of ion-exchange and proton pump hypotheses

1994 ◽  
Vol 266 (2) ◽  
pp. R315-R320 ◽  
Author(s):  
W. T. Potts
Keyword(s):  
Proton Pump ◽  
Competitive Inhibition ◽  
Sodium Ion ◽  
Hydrogen Ion ◽  
Freshwater Species ◽  
Hydrogen Ions ◽  
Sodium Influx ◽  
Sodium Uptake ◽  
Saturation Kinetics ◽  
Kinetics Of

Sodium uptake has been shown to follow saturation kinetics in many freshwater species of animals, and in the presence of hydrogen ions uptake appears to show competitive inhibition. These characteristics are compatible with the hypothesis that uptake occurs via a carrier-mediated exchange of sodium ion for hydrogen ion. However, recently it has been shown that in frog skin, sodium uptake is driven by an electrogenic pump not directly linked to sodium, and evidence is accumulating that a similar pump may occur in other freshwater animals. A mathematical model is developed that shows that a proton pump would also produce saturation kinetics and mimic carrier-mediated competitive inhibition. It would also account for the linkage between sodium influx and efflux observed in several species.

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