scholarly journals Potassium Accumulation and Sodium Efflux by Porphyra perforata Tissues in Lithium and Magnesium Sea Water

1959 ◽  
Vol 43 (1) ◽  
pp. 29-38 ◽  
Author(s):  
Richard W. Eppley
Keyword(s):  
Concentration Gradient ◽  
Marine Alga ◽  
Sea Water ◽  
Secondary Process ◽  
Na Transport ◽  
K Uptake ◽  
Potassium Accumulation ◽  
Sodium Efflux ◽  
Na Efflux ◽  
Red Marine Alga

Cells of Porphyra perforata, a red marine alga, accumulate K in the absence of concomitant Na or Li extrusion while immersed in Li- or Mg-sea waters lacking Na. This suggests that the coupling observed between K and Na transport is facultative. No evidence is obtained for net extrusion of Li. Na efflux, with the concentration gradient, is facilitated by K and is proportional to the cellular Na content. Either Na efflux does not involve an ion carrier or the number of Na sites is large. Because K accumulation has been observed in the absence of Na extrusion, but not vice versa, it seems that K uptake is the primary secretory event, with Na extrusion a secondary process dependent upon K accumulation.

scholarly journals SODIUM EXCLUSION AND POTASSIUM RETENTION BY THE RED MARINE ALGA, PORPHYRA PERFORATA

1958 ◽  
Vol 41 (5) ◽  
pp. 901-911 ◽  
Author(s):  
Richard W. Eppley
Keyword(s):  
Concentration Gradient ◽  
Marine Alga ◽  
Metabolic Inhibitors ◽  
Reduced Sulfur Compounds ◽  
Concentration Gradients ◽  
Potassium Accumulation ◽  
Potassium Loss ◽  
Sodium Extrusion ◽  
Potassium Retention ◽  
Red Marine Alga

Cells of the red marine alga, Porphyra perforata, accumulate potassium and exclude sodium, chloride, and calcium. Various metabolic inhibitors including dinitrophenol, anoxia, and p-chloromercuribenzoate partially abolish the cells' ability to retain potassium and exclude sodium. Iodoacetate induces potassium loss only in the dark; reduced sulfur compounds offer protection against the effects of p-chloromercuribenzoate; dinitrophenol stimulates respiration at concentrations which cause potassium loss and sodium gain. Following exposure to anoxia potassium accumulation and sodium extrusion take place against concentration gradients. These movements are retarded by sodium cyanide, but are stimulated by light. Sodium entry, following long exposure to 0.6 M sucrose, occurs rapidly with the concentration gradient, while potassium entry against the concentration gradient takes place slowly, and is prevented by cyanide.

scholarly journals POTASSIUM-DEPENDENT SODIUM EXTRUSION BY CELLS OF PORPHYRA PERFORATA, A RED MARINE ALGA

1958 ◽  
Vol 42 (2) ◽  
pp. 281-288 ◽  
Author(s):  
Richard W. Eppley
Keyword(s):  
Marine Alga ◽  
Sea Water ◽  
High Sodium ◽  
Low Concentrations ◽  
Carrier Mechanism ◽  
Low Potassium ◽  
Sodium Extrusion ◽  
Rubidium Accumulation ◽  
Red Marine Alga

Potassium-free artificial sea water causes a loss of cell potassium and a gain of cell sodium in Porphyra perforata, which is not attributable to an inhibition of respiration. On adding KCl or RbCl to such low potassium, high sodium tissues, net accumulation of potassium or rubidium takes place, accompanied by net extrusion of sodium. Rates of potassium or rubidium accumulation and sodium extrusion are proportional to the amount of KCl or RbCl added only at low concentrations. Saturation of rates is evident at KCl or RbCl concentrations above 20–30 mM, suggesting the role of an ion carrier mechanism of transport. Evidence for and against mutually dependent sodium extrusion and potassium or rubidium accumulation is discussed.

Osmoregulation by the Prenatal Spiny Dogfish, Squalus Acanthias

1982 ◽  
Vol 101 (1) ◽  
pp. 295-305 ◽  
Author(s):  
DAVID H. EVANS ◽  
AIMO OIKARI ◽  
GREGG A. KORMANIK ◽  
LEIGH MANSBERGER
Keyword(s):  
Sea Water ◽  
Electrical Potential ◽  
Fluid Flows ◽  
Maternal Plasma ◽  
Water Levels ◽  
Squalus Acanthias ◽  
Rectal Gland ◽  
Na Efflux ◽  
Uterine Fluid ◽  
Electrochemical Equilibrium

Late in gestation of the ovoviviparous dogfish, Squalus acanthias, the uterine fluids are essentially sea water, while the plasma of the ‘pup’ is similar to that of the female, i.e. isotonic to sea water/uterine fluids, with significantly less Na and Cl, and substantial concentrations of urea. Early ‘candle’ embryos are bathed in ‘candle’ fluid and uterine fluid which contains Na and Cl concentrations intermediate between maternal plasma and sea water levels, K concentrations above sea water levels, and urea concentrations slightly below those found in the maternal plasma. Both fluids are isotonic to sea water and maternal plasma. Incubation of ‘candles’ with associated embryos in sea water for 4–6 days resulted in significant increases in ‘candle’ fluid Na and Cl concentrations, and a decline in ‘candle’ fluid K and urea levels. However, under these conditions, the ‘candle’ embryo is still able to regulate plasma Na, Cl, K and urea concentrations. The efflux of Cl is approximately 5 times the efflux of Na from the prenatal ‘pup’; however, both effluxes are equivalent to those described for adult elasmobranchs. The transepithelial electrical potential (TEP) across the ‘pup’ is −4.4 mV in sea water, which indicates that both Na and Cl are maintained out of electrochemical equilibrium. Cloacal fluid flows vary diurnally with Na and Cl concentrations significantly above those of the plasma. Rectal gland efflux can account for 50–100% of the Na efflux, but less than 25% of the Cl efflux. Removal of the rectal gland resulted in an increase in plasma Na and Cl concentrations 48 or 72 h after the operation, but in both cases it appears that some extra rectal gland excretory system balances at least some of the net influx of both salts. Our results demonstrate that even very young ‘candle’ embryos of S. acanthias are capable of osmoregulation, and that older embryos (‘pups') osmoregulate against sea water intra-utero and display the major hallmarks of elasmobranch osmoregulation, including a reduced ionic permeability and a functional rectal gland for net extrusion of NaCl. In addition, it appears that other pathways exist for salt extrusion in addition to the rectal gland. Note:

Characteristics of active Na transport in intact cardiac cells

1979 ◽  
Vol 236 (2) ◽  
pp. H189-H199 ◽  
Author(s):  
H. G. Glitsch
Keyword(s):  
Heart Muscle ◽  
Muscle Cells ◽  
Cardiac Cells ◽  
Na Transport ◽  
Concentration Gradients ◽  
Experimental Conditions ◽  
Na Pump ◽  
Na Efflux ◽  
Heart Muscle Cells ◽  
K Concentration

An active Na transport maintains the Na and K concentration gradients across the cell membrane of many cells and restores them following excitation. Heart muscle cells display frequent electrical discharges and thus the cardiac Na pump is of fundamental functional significance. Some methods for studying active Na transport are described. The active Na efflux from heart muscle cells is activated by an increase in the intracellular Na and the extracellular K concentration. The linkage between active Na efflux and active K influx varies widely according to the experimental conditions. The cardiac Na pump is electrogenic and can contribute directly to the membrane potential of the cells. The effects of active Na transport on contraction and intercellular coupling in myocardium are discussed.

scholarly journals CATION TRANSPORT IN YEAST

1956 ◽  
Vol 39 (5) ◽  
pp. 687-704 ◽  
Author(s):  
Ernest C. Foulkes
Keyword(s):  
Cell Membrane ◽  
Dissociation Constant ◽  
Concentration Gradient ◽  
Cation Transport ◽  
K Uptake ◽  
Present Evidence ◽  
Inhibitor Complex ◽  
Maximum Value ◽  
Low Concentrations ◽  
K Transport

1. The distribution of azide added to suspensions of bakers' yeast was studied under various conditions. The recovery of azide was estimated in the volume of water into which low concentrations of electrolytes can readily diffuse (anion space). Considerable azide disappeared from this anion space. 2. The incomplete recovery of azide in the anion space is due to its uptake by the cells. This uptake occurs against a concentration gradient at 0°C., and is attributed to binding of azide by cell constituents. 3. Confirmatory evidence is presented that one such constituent is the K carrier in the cell membrane. The azide inhibition of K transport is not mediated by inhibition of cytochrome oxidase in the mitochondria. 4. From the amount of combined azide and the experimentally determined dissociation constant of the K carrier-inhibitor complex, the maximum value for the concentration of this carrier is calculated as 0.1 µM/gm. yeast. 5. The addition of glucose and PO4 causes a secondary K uptake which is not azide-sensitive and is clearly distinct from the primary, azide-sensitive mechanism. 6. The existence of a separate carrier responsible for Na extrusion is reconsidered. It is concluded that present evidence does not necessitate the assumption that such a carrier is active in yeast.

Physiological Correlates of Interspecific Variation in Acid Tolerance in Fish

1988 ◽  
Vol 136 (1) ◽  
pp. 243-258 ◽  
Author(s):  
J. FREDA ◽  
D. G. MCDONALD
Keyword(s):  
Yellow Perch ◽  
Acid Tolerance ◽  
Binding Activity ◽  
Low Ph ◽  
Whole Body ◽  
Salmo Gairdneri ◽  
Survival Times ◽  
Ion Regulation ◽  
Sodium Efflux ◽  
Na Efflux

This study investigated ion regulation in relation to water pH in three species of fish of differing tolerance to low pH (common shiners, Notropis cornutus, most sensitive; rainbow trout, Salmo gairdneri, intermediate; yellow perch, Perca flavescens, least sensitive). Increasing sensitivity to exposure to low pH was characterized by shorter survival times, greater losses of whole-body ions, more complete inhibition of Na+ uptake, and greater stimulation of Na+ efflux, the latter being the most important factor in determining survival. Interspecific variations in acid tolerance were also correlated with Na+ transport characteristics at circumneutral pH; Km was directly correlated and Vmax inversely correlated with acid tolerance. In addition, there were large qualitative differences among the species in the Ca2+-dependence of Na+ efflux. Sodium efflux induced by low pH was markedly Ca2+-dependent in both trout and shiners in a manner consistent with a simple competition between Ca2+ and H+ for gill binding sites. The increased sensitivity of shiners relative to trout was related to lowered Ca2+- binding activity. In contrast, Na+ efflux in perch was virtually unaffected by water [Ca2+]. Similarly, La3+ (a Ca2+ antagonist) stimulated higher Na+ losses from shiners than from trout, but had little effect upon perch. Ionic losses produced by saturating La3+ concentrations were generally lower than those produced by H+, suggesting that Ca2+ displacement is not the only mechanism for increased gill permeability at low pH. Nonetheless, the results obtained are consistent with the notion that acid tolerance may be related to Ca2+-binding activity in some species (e.g. trout and shiners) although not in others (e.g. perch).

The Ionic Relations of Artemia Salina (L.)

1969 ◽  
Vol 51 (3) ◽  
pp. 739-757
Author(s):  
P. G. SMITH
Keyword(s):  
Sea Water ◽  
Electrical Potential ◽  
Artemia Salina ◽  
Electrical Potential Difference ◽  
External Concentration ◽  
Sodium Efflux ◽  
Exchange Diffusion ◽  
Similar Shape ◽  
Diffusional Permeability ◽  
Free Media

I. The effects of different external media on the sodium and chloride efflux in Artemia salina, the brine shrimp, have been observed, using animals acclimatized to sea water. In sea water, both sodium and chloride fluxes across the epithelium are approximately 7,000 pmole cm.-2 sec.-1. 2. Sodium efflux drops markedly in sodium-free media, and chloride efflux falls in chloride-free media; the two effects are independent, and are not due to changes in external osmolarity. 3. The decreases in sodium efflux can be explained by changes in electrical potential difference and diffusional permeability; exchange diffusion of sodium does not occur. 4. Approximately 70% of the chloride efflux is due to exchange diffusion, and most of the remainder is due to active transport. 5. It is shown that graphs of ion efflux against external concentration which can be fitted by a Michaelis-Menten equation do not constitute evidence for the presence of exchange diffusion; graphs of similar shape can be obtained if the flux is simply diffusional. 6. The drinking rate, determined from the rate of uptake of 131I-polyvinylpyr-rolidone, is 36 pl. sec.-1, or 2.0% body weight hr.-1. 7. The diffusional influx of water is 240 pl. sec.-1.

The effects of transecting the IXth and Xth cranial nerves on hydromineral balance in the eel Anguilla anguilla

1976 ◽  
Vol 64 (2) ◽  
pp. 461-475
Author(s):  
N. Mayer-Gostan ◽  
T. Hirano
Keyword(s):  
Fresh Water ◽  
Sea Water ◽  
Cranial Nerves ◽  
Anguilla Anguilla ◽  
Vagus Nerves ◽  
Rapid Reduction ◽  
Ion Concentrations ◽  
Excess Loss ◽  
Na Efflux ◽  
Hydromineral Balance

The IXth and the Xth cranial nerves in Anguilla anguilla were transected, and the effects upon ion and water balance were studied in fresh water and sea water, and during transfer from fresh water and vice versa. In fresh water there is a slow demineralization due to an excess loss of Na and Cl ions. During freshwater to seawater transfer the eel survives only for 4–5 days. The fish do not drink and Na efflux does not increase enough to extrude excess ions. In sea water the glossopharyngeal and vagus nerves are necessary for the maintenance of the hydromineral balance. Denervation is followed by an increase in plasma ion concentrations. Na fluxes are not modified and increased water loss is not compensated by drinking. The rapid reduction of Na efflux during transfer from sea water to fresh water is not modified by denervation.

The Effect of External Potassium Ions on the Electrical Potential Measured Across the Gills of the Teleost, Dormitator Maculatus

1974 ◽  
Vol 61 (2) ◽  
pp. 277-283
Author(s):  
DAVID H. EVANS ◽  
JEFFREY C. CARRIER ◽  
MARGARET B. BOGAN
Keyword(s):  
Sea Water ◽  
Electrical Potential ◽  
Potassium Ions ◽  
Sodium Efflux ◽  
Electrical Potentials ◽  
External Potassium ◽  
Potassium Influx ◽  
Sodium Extrusion ◽  
Sufficient Magnitude ◽  
Stimulation Of

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.

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