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

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.

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.


1964 ◽  
Vol 47 (6) ◽  
pp. 1209-1227 ◽  
Author(s):  
J. Maetz ◽  
F. García Romeu

The addition of ammonium ions to the external medium results in an inhibition of the sodium influx and net uptake in Carassius auratus, while intraperitoneal injection of ammonium produces the opposite effect. The simultaneous chloride balance is not significantly affected by these treatments. The addition of bicarbonate ions to the external medium results in a reduction of the influx and net flux of chloride, while injection of bicarbonate produces the opposite effect. The simultaneous sodium balance is not significantly altered. The effects of the external additions are reversible after elimination of the excess ammonium or bicarbonate ions by rinsing. Inhibition of carbonic anhydrase in the gill by injection of acetazoleamide produces a simultaneous inhibition of both sodium and chloride exchanges. These results confirm the hypothesis of an exchange of sodium for ammonium, and of bicarbonate for chloride across the gill. A tentative schematic representation of the ionic absorption mechanisms in the branchial cell of the fresh-water teleosts is given. Similarities with other biological membranes and especially with the renal tubule are pointed out.


1959 ◽  
Vol 36 (1) ◽  
pp. 126-144 ◽  
Author(s):  
J. SHAW

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.


1975 ◽  
Vol 62 (1) ◽  
pp. 157-174
Author(s):  
DA Wright

In fourth instar larvae of Camptochironomus tentans, net sodium uptake from 2 mM-NaCl has an electrogenic component. During net uptake the transepithelial potential (TEP) alters from a value of approximately - 40 mV (sign refers to haemolymph), in depleted animals, to approximately o mV. The TEP in depleted larvae is dependent upon external sodium concentration above about I mM-Na+, becoming increasingly electropositive (haemolymph relative to medium) at high sodium concentrations. This effect is exaggerated in Na2SO4 compared with NaCl. At an external concentration of 2mM-NaCl, chloride is carried by an electroneutral mechanism, probably a closely coupled Cl-/anion exchange. However, it is possible that chloride transport could become somewhat electrogenic at higher concentrations. Lithium competes with sodium for the electrogenic pump. Observed TEPs differ greatly from those required to maintain passively the haemolymph concentrations of sodium and chloride.


1970 ◽  
Vol 52 (2) ◽  
pp. 275-290
Author(s):  
R. MORRIS ◽  
J. M. BULL

1. Sodium influx in ammocoete larvae increases exponentially with external sodium concentration (0-1.0 mM/l.) and sodium-depleted animals show a 20% increase compared with normal animals. 2. Sodium loss decreases as the environmental concentration decreases, although the reverse situation is expected from considering diffusion outflux alone. 3. It is argued that part of the sodium loss is back-transported by the transport mechanism and this accounts for the reduced sodium loss from sodium-depleted animals whose sodium carrier activity is increased. The curves relating back-transport to environmental sodium differ from those derived by Kirschner for isolated frog skin. 4. Sodium influx increases as sodium loss increases, indicating a self mechanism whose features are discussed. In the ammocoete, the sodium carrier mechanism appears to change in affinity for sodium (short-term response) and can also change in concentration (long-term response), and it is suggested that these features, together with permeability changes, may form the basis of the controlling mechanism for sodium balance.


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.


1997 ◽  
Vol 322 (3) ◽  
pp. 693-699 ◽  
Author(s):  
Elke R. GIZEWSKI ◽  
Ursula RAUEN ◽  
Michael KIRSCH ◽  
Irith REUTERS ◽  
Herbert DIEDERICHS ◽  
...  

Hypothermia, as used for organ preservation in transplantation medicine, is generally supposed to lead to an intracellular accumulation of sodium, and subsequently of chloride, via inhibition of the Na+/K+-ATPase. However, on studying the cellular sodium concentration of cultured liver endothelial cells using fluorescence microscopy, we found a 55% decrease in the cellular sodium concentration after 30 min of cold incubation in University of Wisconsin (UW) solution. To confirm this surprising result, we set up a capillary electrophoresis method that allowed us to determine the cellular contents of inorganic cations and of inorganic anions. Using this method we measured a decrease in the cellular sodium content from 104±11 to 55±4 nmol/mg of protein, accompanied by a decrease in the chloride content from 71±9 to 25±5 nmol/mg of protein, after 30 min of cold incubation in UW solution. When the endothelial cells were incubated in cold Krebs–Henseleit buffer or in cold cell culture medium instead of UW solution, similar early decreases in cellular sodium and chloride contents were observed, thus excluding the possibility of the decreases being dependent on the preservation solution used. Furthermore, experiments with cultured rat hepatocytes yielded a similar decrease in sodium content during initiation of cold incubation in UW solution, so the decrease does not appear to be cell-specific either. These results suggest that, contrary to current opinion, sodium efflux predominates over sodium influx during the early phase of cold incubation of cells.


1968 ◽  
Vol 21 (5) ◽  
pp. 871 ◽  
Author(s):  
MG Pitman ◽  
AC Courtice ◽  
Barbara Lee

Measurements are described of the uptake of sodium and potassium by barley roots at low salt status. It was found that initially there was little preference for potassium in the salt accumulated, but about 5 hr after the start of salt accumula� tion net uptake of sodium decreased markedly, and thereafter much more potassium was taken up than sodium. The roots reached salt saturation in about 24 hr. The decreased sodium uptake was due to a reduction in sodium influx.


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.


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