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

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.

1970 ◽  
Vol 53 (1) ◽  
pp. 147-163 ◽  
Author(s):  
PETER GREENAWAY

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.


1987 ◽  
Vol 131 (1) ◽  
pp. 417-425
Author(s):  
W. J. FRAIN

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.


1967 ◽  
Vol 46 (3) ◽  
pp. 499-518
Author(s):  
D. W. SUTCLIFFE

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.


1961 ◽  
Vol 38 (1) ◽  
pp. 1-15
Author(s):  
J. SHAW ◽  
D. W. SUTCLIFFE

1. The mechanisms of sodium balance in Gammarus duebeni and G. pulex, adapted to various external concentrations, were compared. 2. G. duebeni could be adapted to live in 1 mm/l. NaCl solution and, in some cases, to concentrations down to 0.2 mM/l. G. pulex could survive in concentrations as low as 0.06 mM/l. 3. The sodium loss rate in G. duebeni adapted to 2% sea water was much higher than in G. pulex but was reduced to about the same level when the animals were adapted to low external concentrations. 4. In both species there was a non-linear relationship between sodium influx and the external sodium concentration. In G. duebeni the uptake mechanism was saturated at an external concentration of about 10 mM/l., whereas in G. pulex saturation was reached at a much lower concentration. The maximum rate of uptake was greater in G. duebeni than in G. pulex. 5. In both species adaptation to low concentrations involved a small increase in the sodium influx and a reduction in the loss rate. 6. The most important factor in the superiority of G. pulex over G. duebeni in surviving at low external concentrations is the high affinity for sodium displayed by the uptake mechanism in G. pulex.


1972 ◽  
Vol 55 (1) ◽  
pp. 195-201 ◽  
Author(s):  
D. R. FERGUSON ◽  
M. W. SMITH

SUMMARY A technique is described by which the unidirectional influx of sodium into toad bladder mucosal cells can be measured over short periods. The uptake of sodium, which is linear over a 60 s contact period, changes in a non-linear way when the external sodium concentration is varied from 5 to 115mm. Vasotocin applied to the serosal surface increases significantly the influx of sodium; amiloride applied to the mucosal surface inhibits influx. This is true whether high or low concentrations of sodium are used to bathe the mucosal surface. The kinetics for the unidirectional influx of sodium provide direct evidence that the passage of sodium into this tissue is by some means other than simple diffusion.


1961 ◽  
Vol 38 (1) ◽  
pp. 135-152
Author(s):  
J. SHAW

1. The mechanism of sodium balance in Carcinus maenas has been investigated. 2. Measurements of sodium outflux showed no evidence of a decrease in surface permeability to sodium in dilute sea water. 3. The rate of urine production in normal sea water was 3.6% body weight per day and the sodium loss through the urine was insignificant compared with the total sodium loss. In 40% sea water the urine rate was increased to 30% body weight per day and the loss in the urine accounted for 20% of the total loss. 4. Measurements of sodium influx and calculation of the active component showed that the active uptake mechanism was fully saturated at all external concentrations in which the animals could survive. 5. Regulation of the blood sodium concentration is effected largely by the activation of the sodium uptake mechanism. This prevents the blood concentration falling below a critical level as long as the external concentration itself is not too low.


1965 ◽  
Vol 42 (1) ◽  
pp. 29-43 ◽  
Author(s):  
R. H. STOBBART

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.


1978 ◽  
Vol 235 (1) ◽  
pp. R35-R40 ◽  
Author(s):  
T. H. Dietz

Freshwater bivalves maintain a Na steady state in artificial pondwater: JiNa = 1.2 +/- 0.1 mumol/g dry tissue per h. Na uptake is Cl independent. The affinity (KS) of the Na transport system is 0.15-0.23 mmol Na/1. Sodium influx is coupled to H and/or NH4 exchange. Salt depletion stimulates JiNa 300% relative to nondepleted animals with no change in Ks. Injected ammonium ion stimulates JiNa. Sodium transport is inhibited 84% by 0.5 mM amiloride but is not affected by 4 mM NH4 or 1 mM furosemide in the bathing solution or injection of acetazolamide (0.26 mumol/ml blood).


1960 ◽  
Vol 37 (3) ◽  
pp. 534-547
Author(s):  
J. SHAW

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.


1985 ◽  
Vol 223 (1233) ◽  
pp. 449-457 ◽  

A study has been made with human red cells of sodium movements that are sensitive to the drug furosemide. The aim was to see if furosemide-sensitive movements that are symmetrical (exchange) became asymmetrical (net transport) on replacement of chloride with nitrate as the major external anion. Cells were incubated for 4 h at 37 °C with 140 mm sodium, and chloride or nitrate as the principal anion. Under a variety of conditions (presence and absence of ouabain or furosemide, or both) the cell sodium concentration was always higher when chloride was replaced with nitrate. The cells became leakier to sodium. Tracer studies indicated that, in contrast to the results in chloride medium, the decrease in sodium influx was greater than the fall in efflux when furosemide was added to cells in nitrate medium. The results confirm that the sensitivity of sodium efflux to furosemide depended on chloride. However, influx showed a different sensitivity in that furosemide still inhibited in cells incubated in nitrate medium. The stimulation of sodium influx with nitrate medium was independent of external potassium (10–50 mm) and the furosemide-sensitive influx was also constant. It is concluded that symmetrical transmembrane sodium movements with cells in chloride medium became downhill asymmetrical in nitrate medium, giving a net gain of cell sodium that was insensitive to ouabain and sensitive to furosemide. The drug thus partly retarded the gain of cell sodium that otherwise occurred in the somewhat leaky cells.


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