The energy requirement for sodium extrusion from a frog muscle

Parallel measurements have been made of the oxygen consumption and efflux of radioactive sodium in pairs of frog sartorius muscles. Calculation of the amount of secretory work necessary for an active extrusion of sodium at the observed rate showed that it would involve the utilization of about one-tenth of the energy available from resting metabolism.This figure may reasonably be regarded as a lower limit to the efficiency of the secretory mechanism. Some of the measurements were made in a potassium-free Ringer’s solution, and others with an external potassium concentration of 10mM. In the potassium-rich medium, both the sodium efflux and the oxygen consumption were increased, the proportion of the energy production required for sodium extrusion remaining roughly constant. The action of dinitrophenol and other metabolic inhibitors on the sodium efflux in sartorius muscles was examined, but there were no very obvious effects.

1974 ◽  
Vol 61 (2) ◽  
pp. 277-283
Author(s):  
DAVID H. EVANS ◽  
JEFFREY C. CARRIER ◽  
MARGARET B. BOGAN

1. A technique has been developed for the measurement of electrical potentials (TGP's) across the gills of free-swimming, Dormitator maculatus. 2. Transfer of fish to various KCl solutions is correlated with changes in the TGP, which are not of sufficient magnitude to account for the known potassium stimulation of sodium efflux from this species. 3. Transfer to potassium-free sea water results in little or no change in TGP while previous results have shown that such a transfer is correlated with a 22% reduction of sodium efflux. 4. Transfer to fresh water results in a reduction of TGP from +17 mV (inside positive) to -36 mV which is sufficient to account for the instantaneous reduction in sodium efflux previously shown for this species. 5. It is concluded that while changes in TGP can account for the ‘Na-free effect’ in D. maculatus they cannot account for the potassium effects on sodium extrusion. This supports the previous conclusion that sodium efflux and potassium influx are chemically linked in this species.


Author(s):  
E. E. Bittar ◽  
P. C. Caldweix ◽  
A. G. Lowe

The efflux of radioactive sodium injected into single muscle fibres from the leg muscles of Maia squinado (Herbst) has been studied. The efflux is reduced by the sodium-pump-inhibitor ouabain and by removal of the external potassium. An increase in external potassium leads to a transient increase in sodium efflux which is then followed by a decline to a value well below the normal level. Externally applied caffeine and injected calcium can, under certain conditions, cause a lowering of the sodium efflux which may be associated with contraction of the fibre. The injection of lactate and pyruvate did not affect the efflux. The results are discussed in terms of the possible effects of the structure of the fibre on the efflux.


1971 ◽  
Vol 57 (2) ◽  
pp. 164-187 ◽  
Author(s):  
R. A. Sjodin

After a 20 min initial washout, the rate of loss of radioactively labeled sodium ions from sodium-enriched muscle cells is sensitive to the external sodium and potassium ion concentrations. In the absence of external potassium ions, the presence of external sodium ions increases the sodium efflux. In the presence of external potassium ions, the presence of external sodium ions decreases the sodium efflux. In the absence of external potassium ions about one-third of the Na+ efflux that depends upon the external sodium ion concentration can be abolished by 10-5 M glycoside. The glycoside-insensitive but external sodium-dependent Na+ efflux is uninfluenced by external potassium ions. In the absence of both external sodium and potassium ions the sodium efflux is relatively insensitive to the presence of 10-5 M glycoside. The maximal external sodium-dependent sodium efflux in the absence of external potassium ions is about 20% of the magnitude of the maximal potassium-dependent sodium efflux. The magnitude of the glycoside-sensitive sodium efflux in K-free Ringer solution is less than 10% of that observed when sodium efflux is maximally activated by potassium ions. The inhibition of the potassium-activated sodium efflux by external sodium ions is of the competitive type. Reducing the external sodium ion concentration displaces the plots of sodium extrusion rate vs. [K]o to the left and upwards.


1982 ◽  
Vol 80 (1) ◽  
pp. 125-147 ◽  
Author(s):  
M Haas ◽  
W F Schmidt ◽  
T J McManus

The transient increase in cation permeability observed in duck red cells incubated with norepinephrine has been shown to be a linked, bidirectional, co-transport of sodium plus potassium. This pathway, sensitive to loop diuretics such as furosemide, was found to have a [Na + K] stoichiometry of 1:1 under all conditions tested. Net sodium efflux was inhibited by increasing external potassium, and net potassium efflux was inhibited by increasing external sodium. Thus, the movement of either cation is coupled to, and can be driven by, the gradient of its co-ion. There is no evidence of trans stimulation of co-transport by either cation. The system also has a specific anion requirement satisfied only by chloride or bromide. Shifting the membrane potential by varying either external chloride (at constant internal chloride) or external potassium (at constant internal potassium in the presence of valinomycin and DIDs [4,4'-diisothiocyano-2,2'-disulfonic acid stilbene]), has no effect on nor-epinephrine-stimulated net sodium transport. Thus, this co-transport system is unaffected by membrane potential and is therefore electrically neutral. Finally, under the latter conditions-when Em was held constant near EK and chloride was not at equilibrium-net sodium extrusion against a substantial electrochemical gradient could be produced by lowering external chloride at high internal concentrations, thereby demonstrating that the anion gradient can also drive co-transport. We conclude, therefore, that chloride participates directly in the co-transport of [Na + K + 2Cl].


1973 ◽  
Vol 58 (3) ◽  
pp. 627-636
Author(s):  
DAVID H. EVANS ◽  
CHARLES H. MALLERY ◽  
LARRY KRAVITZ

1. The effect of external potassium ions on the extrusion of sodium ions by the seawater-acclimated fat sleeper, Dormitator maculatus, was investigated. 2. Removal of external potassium ions reduced the efflux of sodium from the fish by 22% while addition of 10-4 M ouabain reduced the efflux of sodium ions by 14%. 3. Addition of potassium ions to distilled-water baths into which fish were rapidly transferred stimulated sodium extrusion in a manner which could be described by the Michaelis-Menten equation. The Km of this potassium-stimulated sodium efflux was approximately 2 mM-K/1. 4. The calculated rate of sodium extrusion was 10 times the oral ingestion of sodium ions. 5. Biochemical assays of the levels of the enzyme Na-K-activated ATPase extracted from gill tissue determined that seawater-acclimated fish had 3 times the enzymic activity that fish acclimated to freshwater had. 6. In vitro potassium stimulation of the extracted Na-K-activated ATPase showed Michaelis-Menten kinetics with a Km of approximately 2 mM-K/l. 7. It is concluded that the extrusion of sodium ions by Dormitator maculatus acclimated to sea water is coupled with potassium uptake and is mediated by the enzyme Na-K-activated ATPase.


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.


1995 ◽  
Vol 198 (2) ◽  
pp. 349-358 ◽  
Author(s):  
S Piller ◽  
R Henry ◽  
J Doeller ◽  
D Kraus

Callinectes sapidus and C. similis co-occur in estuarine waters above 15 salinity. Callinectes sapidus also inhabits more dilute waters, but C. similis is rarely found below 15 . Previous work suggests that C. sapidus may be a better hyperosmoregulator than C. similis. In this study, energy metabolism and the levels of transport-related enzymes in excised gills were used as indicators of adaptation to low salinity. Oxygen consumption rates and mitochondrial cytochrome content of excised gills increased in both species as acclimation salinity decreased, but to a significantly greater extent in C. similis gills. In addition, C. similis gills showed the same levels of carbonic anhydrase and Na+/K+-ATPase activities and the same degree of enzyme induction during low-salinity adaptation as has been reported for C. sapidus gills. However, hemolymph osmolality and ion concentrations were consistently lower in C. similis at low salinity than in C. sapidus. Therefore, although gills from low-salinity-acclimated C. similis have a higher oxygen consumption rate and more mitochondrial cytochromes than C. sapidus gills and the same level of transport-related enzymes, C. similis cannot homeostatically regulate their hemolymph to the same extent as C. sapidus.


1978 ◽  
Vol 235 (1) ◽  
pp. C63-C68 ◽  
Author(s):  
R. F. Abercrombie ◽  
P. de Weer

The operation of the sodium pump of giant axons of the squid, Loligo pealei, has been studied simultaneously in two independent ways: 1) by measuring sodium efflux with 22Na, and 2) by calculating the transmembrane current generated by the pump from measurements of membrane resistance and digitalis-sensitive membrane potential. In normal, untreated axons, the effect of increasing the external potassium concentration on both sodium efflux and pump current is similar, which suggests that Na:K pump stoichiometry remains relatively constant in the range of 0-20 mM external K. The data are compatible with a 3:2 Na:K ratio. In axons whose intracellular ADP level has been elevated by injection of L-arginine, a large, electrically silent, cardiotonic steroid-sensitive sodium efflux takes place in the absence of external potassium; this suggests that pump-mediated Na:Na exchange is 1:1 or electroneutral. Finally, elevation of external potassium levels causes the appearance, in high-ADP axons, of electrogenic pumping, with little effect on sodium efflux; hence, in contrast to what is seen in normal (low-ADP) axons, the charge translocated, per sodium ion extruded, increases sharply with increasing extracellular potassium levels.


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