Sodium Ion Activity Research Articles

Sulfonate Retention by Kaolinite at High pH—Effect of Inorganic Anions

Summary At high pH and with surfactant concentrations well above the critical micelle concentration (CMC), the pH-dependent part of adsorption is small. Retention depends especially on the sodium-ion activity and on the type and valence of inorganic anions. As the anionic charge increases, adsorption at a given ionic strength decreases. This behavior correlates with the effect of anions on the sulfonate activity in solution.

Sodium-selective electrodes based on PVC membranes containing bis[(3 n+1)-crown- n] ether derivatives

The cationic selectivity and electrode characteristics of poly(vinyl chloride) (PVC) membranes based on bis[(3 n+1-crown- n] ethers are discussed. The electrodes exhibit Nernstian responses over the sodium ion activity range 1×10 −5–1 M and can be applied over the pH range 2–10. The sodium selectivity of the PVC membranes increases with decrease in the biscrown ether ring size. The membrane based on bis(10-crown-3)-hexamethylenebis(3,6,10-trioxacycloundecane) has k Na,K pot=6.15×10 −3 and the detection limit for sodium cations is (6±0.5)×10 −6 M.

Counterion activity in dilute salt-free solutions of some anionic polyelectrolytes

This paper presents experimental data on sodium ion activities obtained by two methods in salt-free solutions for four anionic polyelectrolytes in their completely neutralized sodium salt form. Treatment of the data reveals some quantitative disagreement with theoretical predictions although there is considerable qualitative agreement with the main proposition of Manning's counterion condensation theory. A striking disparity between potentiometric and osmometric results is noted and an explanation is offered.

Sodium ion activity and electrical conductivity of poly(maleic acid) and poly(isobutylene-alt-maleic acid) in aqueous salt-free solution

The effect of charge density and distribution of charged groups in the polyelectrolyte chain on the counterion binding was studied. The values of the activity coefficient of Na + in poly(maleic acid) (PMA) under salt-free conditions deviated from those predicted by the theories of Manning and Katchalsky-Lifson. The same tendency was observed in the copolymer (PIM) for higher dissociation degrees regions. The results suggest that the bound sodium ions are fairly labile for dissociation degrees higher than 0.5 in dilute, salt-free solutions of PMa and PIM.

Effects of halothane on intracellular sodium ion activity under condition of sodium pump inhibition in dog Purkinje fibers

Effects of halothane on intracellular sodium ion activity under condition of sodium pump inhibition in dog Purkinje fibers

Ototoxic Effect of Potassium Canrenoate on the Guinea Pig Cochlea

Potassium canrenoate (PC) is a diuretic with antialdosterone action, reducing the reabsorption of sodium in the efferent renal tubules. This drug has been reported to damage only the marginal cells of the stria vascularis in the cochlea. The perilymphatic space of the guinea pig cochlea was perfused with an artificial perilymph containing 5 x 10(-3) M potassium canrenoate. Following the onset of perfusion, the endocochlear dc potential (EP) gradually declined to around 10 mV but did not become negative even when the perfusion was continued. A similar decrease in EP was observed in kanamycin-deafened guinea pigs. When the respirator was turned off and perfusion discontinued, a large negative EP appeared during 5 min of anoxia in normal guinea pigs but not in the kanamycin-deafened guinea pigs. The decreased EP recovered to preanoxic level after resumption of ventilation. The cochlear microphonics (CM) also gradually declined in parallel with the EP. The summating potential (SP) showed only a minor change. The potassium ion activity in the endolymph decreased slightly but the sodium ion activity remained unchanged during perfusion. These findings suggest that the main target of the PC is the cells of the stria vascularis.

Acceleration of H+ extrusion via Na(+)-H+ exchange in guinea-pig ventricular papillary muscle under intracellular acidic condition.

We investigated mechanisms by which intracellular pH was regulated under intracellular acidic condition in resting guinea-pig ventricular papillary muscles in vitro. Intracellular sodium ion activity (aiNa), intracellular and surface pH (pHi and pHs) were measured with Na(+)- and H(+)-selective microelectrodes and resting tension was measured. By exposure to 0 mM K solution aiNa and resting tension increased progressively while pHi decreased but reached the steady level of pH 6.95. pHs which was lower than external bulk pH (pHo) decreased progressively by exposure to 0 mM K solution. In 4 mM K solution, amiloride (1 mM), an inhibitor of Na(+)-H+ exchange, induced a reversible decrease in both aiNa and pHi, and an increase in pHs. Changes in pHi and pHs induced by application of amiloride in 0 mM K solution were larger than those in 4 mM K solution. The rate of decrease in pHi induced by amiloride became larger at longer exposure to 0 mM K solution. Lowering pHo from 7.4 to 6.4 induced a larger decrease in pHi in 0 mM K solution than that in 4 mM K solution. Lowering pHo from 7.4 to 5.4 reversed the difference between pHs and pHo. These results suggest that in guinea-pig papillary muscle, Na(+)-H+ exchange is active to regulate intracellular H+ under resting condition and under intracellular acidic condition, H+ extrusion via the Na(+)-H+ exchange would be accelerated not only by the net thermodynamic driving force for Na+ and H+ but also by other factors.

Counterion binding by surfactant/?-cyclodextrin inclusion complexes

Sodium ion activities were determined potentiometrically in sodium dodecylsulfate and sodium dodecanoate solutions containingβ-cyclodextrin. Whereas sodium ion did not bind withβ-cyclodextrin, its activity decreased noticeably when the 1:1β-cyclodextrin/surfactant inclusion complex was formed in solution. When the anionic guest was methyl red or methyl orange, no sodium ion binding occurred. When the guest was the cationic dodecylammonium ion in chloride solutions containingβ-cyclodextrin, pronounced chloride ion binding to the 1:1 inclusion complex occurred.

Acidification and intracellular sodium ion activity during stimulated myocardial ischemia

With the use of microelectrodes, intracellular pH (pHi), surface pH (pHs), and intracellular Na+ activity (aiNa) were measured in isolated guinea pig papillary muscles during normal superfusion and during a reversible condition of simulated ischemia. Acid loading by NH+4 prepulse or by CO2-HCO3- addition during superfusion with pH 7.4 solutions caused internal acidification followed by a recovery of pHi, which could be inhibited by amiloride. pHi recovery was associated with an amiloride-sensitive peak rise of aiNa and membrane hyperpolarization, indicative of Na(+)-H+ exchange. Peak increase of aiNa was absent if the pH of the superfusion solution was concomitantly lowered. Imposed ischemia after control superfusion caused membrane depolarization and acidification of pHi and pHs. The change of pHs consistently was larger than that of pHi. aiNa decreased from 5.5 to 4.6 mM after 10-min ischemia. Enlarging the pHi (and pHs) decrease in ischemia by prior reduction of the tissue buffer capacity (CO2-HCO3(-)-free superfusion) was unable to induce a rise of aiNa during the subsequent ischemic period. Amiloride had no significant effect on aiNa during ischemia. It is concluded that the important acidification of pHs reduces the rate of pHi regulatory Na(+)-H+ exchange and thereby contributes to a longer maintenance of the Na+ electrochemical gradient in ischemic cardiac muscle.

Sequence dependent effects in methylphosphonate deoxyribonucleotide double and triple helical complexes

Deoxyribooligonucleotides containing 19 repeating bases of A, T or U were prepared with normal phosphodiester (dA19, dT19, dU19) or methylphosphonate (dA*19, dT*19, dU*19) linkages. Complexes of these strands have been investigated at 1:1 and 1:2 molar ratios (purine:pyrimidine) by thermal melting and gel electrophoresis. There are dramatic sequence dependent differences in stabilities of complexes containing methylphosphonate strands. Duplexes of dA*19 with dT19 or dU19 have sharp melting curves, increased Tm values, and slopes of Tm versus log (sodium ion activity) plots reduced by about one half relative to their unmodified 'parent' duplexes. Duplexes of dA19 with either dT*19 or dU*19, however, have broader melting curves, reduced Tm values at most salt concentrations and slopes of less than one tenth the values for the unmodified duplexes. Duplex stabilization due to reduced phosphate charge repulsion is offset in the pyrimidine methylphosphonate complexes by steric and other substituent effects. Triple helical complexes with dA19 + 2dT19 and dA19 + 2dU19, which can be detected by biphasic melting curves and gel electrophoresis, are stable at increased Na+ or Mg+2 concentrations. Surprisingly, however, no triple helix forms, even at very high salt concentrations, when any normal strand(s) is replaced by a methylphosphonate strand. Since triple helical complexes with methylphosphonates have been reported for shorter oligomers, inhibition with larger oligomers may vary due to their length and extent of substitution.

A novel urushi matrix sodium ion-selective field-effect transistor

A durable sodium ion-selective field-effect transistor (ISFET) is proposed with Urushi as the membrane matrix. The sodium ion-sensing membrane is composed of sodium ionophore (ETH 227), di-2-ethylhexylphthalate, potassium tetrakis( p-chlorophenyl)borate and Urushi. The prepared Urushi matrix ISFET showed a linear response in the sodium ion activity range from 100 M to 10 −3.5 M and about 53 mV per decade change of sodium ion activity. The selectivity of the Urushi matrix ISFET was almost the same as that of the corresponding PVC matrix ion-selective electrode. The Urushi ISFET showed excellent stability with drift below 0.15 mV per hour and durability for over a month, because of strong adhesion of the membrane to the Si 3N 4 gate.

Role of Na+/H+ exchange in the control of intracellular pH and cell membrane conductances in frog skin epithelium.

Ion-sensitive microelectrodes and current-voltage analysis were used to study intracellular pH (pHi) regulation and its effects on ionic conductances in the isolated epithelium of frog skin. We show that pHi recovery after an acid load is dependent on the operation of an amiloride-sensitive Na+/H+ exchanger localized at the basolateral cell membranes. The antiporter is not quiescent at physiological pHi (7.1-7.4) and, thus, contributes to the maintenance of steady state pHi. Moreover, intracellular sodium ion activity is also controlled in part by Na+ uptake via the exchanger. Intracellular acidification decreased transepithelial Na+ transport rate, apical Na+ permeability (PNa) and Na+ and K+ conductances. The recovery of these transport parameters after the removal of the acid load was found to be dependent on pHi regulation via Na+/H+ exchange. Conversely, variations in Na+ transport were accompanied by changes in pHi. Inhibition of Na+/K+ ATPase by ouabain produced covariant decreases in pHi and PNa, whereas increases in Na+ transport, occurring spontaneously or after aldosterone treatment, were highly correlated with intracellular alkalinization. We conclude that cytoplasmic H+ activity is regulated by a basolateral Na+/H+ exchanger and that transcellular coupling of ion flows at opposing cell membranes can be modulated by the pHi-regulating mechanism.

Regulation of cytosolic free calcium in isolated perfused proximal tubules of Necturus.

To study the role of intracellular Ca2+ in regulating renal tubular transport of ions and water, cytosolic calcium ion activity (aiCa), cytosolic sodium ion activity (aiNa), and intracellular pH (pHi) in cells of isolated perfused proximal tubules of Necturus kidney were measured with Ca2+-, Na+-, and H+-selective microelectrodes, respectively. In control conditions, i.e., HCO3-Ringer solution on both sides of the epithelium, aiCa was 82 +/- 7 (SE) nM (n = 54), aiNa averaged 12.8 +/- 0.4 mM (n = 53), and pHi was 7.33 +/- 0.03 (n = 27). When the Na-K pump was inhibited by nominally K-free Ringer circumfusion, aiCa increased from a control level of 75 +/- 13 to 237 +/- 40 nM (paired t test; n = 16; P less than 0.001); in a different set of tubules, aiNa rose from 11.3 +/- 0.6 to 51.5 +/- 5.8 mM (n = 11; P less than 0.001). When organic solutes were deleted in the luminal perfusate, aiCa decreased from 73 +/- 11 to 61 +/- 11 nM (n = 9; P less than 0.001) and aiNa decreased from 14.6 +/- 0.6 to 8.3 +/- 0.7 mM (n = 9; P less than 0.001). Depolarization of the peritubular cell membrane with high-K, low-Na Ringer decreased aiCa from 90 +/- 12 to 55 +/- 9 nM (n = 13; P less than 0.001) and reduced aiNa from 13.1 +/- 1.0 to 7.5 +/- 0.6 mM (n = 16; P less than 0.001). Ionomycin (2 X 10(-6) M) increased aiCa from 67 +/- 10 to 158 +/- 26 nM (n = 10; P less than 0.001) and pHi from 7.33 +/- 0.03 to 7.39 +/- 0.03 (n = 27; P less than 0.001) but reduced aiNa from 11.8 +/- 0.9 to 10.3 +/- 0.7 mM (n = 11; P less than 0.001). The data are consistent with the view that aiCa is determined, in part, by the magnitude of the electrochemical potential gradient for Na ions across the basolateral cell membrane.

Schistosoma mansoni: Measurement of Na + ion activity in the tegument and the extracellular spaces using ion-selective microelectrodes

Ion-selective microelectrodes were used to measure sodium ion activity ( a Na) in the tegument and interstitial spaces in adult male Schistosoma mansoni. In RPMI 1640, a Na averaged 31 ± 13 m M in the tegument, a value significantly less than that in the bathing medium. In the interstitial spaces, it averaged 72 ± 17 m M, a value nearly the same as that in the bathing medium. In hypo- or hyperosmotic media, a Na in the interstitial spaces varied by a value commensurate with change in a Na in the medium, but a Na in the tegument was changed by only a small amount. Monensin (10 μ M), low temperature (20 C), and ouabain (0.3 to 10 μ M) all caused significant increases in a Na in the tegument. Hypo- and hyperosmotic media produced initial weight changes followed by gradual recovery back toward original weights. It is concluded that the schistosome is a volume regulating osmoconformer with osmolality of the extracellular fluid approximating that of the bathing medium, but that within the tegument of the parasite, Na + concentration is controlled by active transport processes.

Intracellular sodium ion activity: reliable measurement and stimulation-induced change in cardiac Purkinje fibers.

Recently Na+-selective microelectrodes (NaSM) have been used to measure quantitatively small changes in intracellular sodium ion activity (aiNa) and to determine a precise time course of comparatively rapid change in aiNa. In such studies, accurate measurement of aiNa requires the following criteria: (i) NaSM should have a fast response time and (ii) an NaSM and a conventional voltage microelectrode should measure the same membrane potential. These criteria were evaluated by measuring aiNa when membrane potential of cardiac Purkinje fibers was suddenly hyperpolarized and depolarized by changing stimulation rate. The NaSM coated with a conductive silver paint had fast response times so that rapid changes in aiNa could be reliably measured. The cardiac Purkinje fibers stimulated at a constant rate generated uniform membrane voltage and the NaSM and conventional microelectrode measured virtually the same membrane potential. This result is somewhat different from that reported under voltage-clamp condition by other investigators. The aiNa of the fibers increased as the stimulation rate was increased over the range of 0.5-3 Hz. In fibers stimulated at 1 Hz, cessation of stimulation was immediately followed by an exponential decline of aiNa with an average time constant of 53 +/- 9 s (SD, n = 8), or rate constant of 0.020 +/- 0.004/s. Restimulation of the fibers produced an exponential rise of aiNa with an average time constant of 65 +/- 12 s (n = 8). Similar results were obtained in fibers stimulated at 2 Hz.(ABSTRACT TRUNCATED AT 250 WORDS)

The ionic basis of the anti-ischemic and anti-arrhythmic properties of magnesium in the heart.

The role of magnesium (Mg) in the prevention of ischemia-induced injury during cardioplegic arrest and in the treatment of cardiac arrhythmias has been considered. Although Mg possesses negative inotropic properties, potassium (K) is more effective than Mg in inducing cardiac arrest. The rationale for the inclusion of Mg in cardioplegic solutions therefore lies not in its cardioplegic properties, but in its ability to influence other cellular events such as the loss of Mg and K and perhaps to counter the detrimental effects of ischemia by antagonizing calcium (Ca) overload. Most of the Mg in the cardiac cell is complexed with high energy phosphate compounds and the loss of Mg during ischemia may restrict the repletion of ATP upon reperfusion and so impair the return of normal contractile function. The ability of Mg to limit K efflux from the cell is of importance not only in the prevention of ischemia-induced K loss but also in the treatment of digitalis-induced arrhythmias. Elevation of extracellular Mg has been shown to reduce the intracellular sodium ion activity ([Na]i) and this decline in [Na]i can be related to the negative inotropic properties of Mg. Mg may therefore exert some of its antiarrhythmic and antiischemic effects by limiting [Na]i-stimulated Ca influx (or facilitating Ca efflux) and hence preventing cellular Ca overload.

Intracellular K+ activity, intracellular Na+ activity and maximum diastolic potential of canine subendocardial Purkinje cells from one-day-old infarcts.

The basis for the reduced maximum diastolic potential of canine cardiac subendocardial Purkinje fibers surviving one day after extensive transmural infarction was investigated, using double-barrel potassium and sodium ion-sensitive microelectrodes. The maximum diastolic potential of Purkinje fibers in infarct preparations from the left ventricular apex measured during the first hour of superfusion in a tissue bath was -50.1 +/- 13.7 mV, a value markedly reduced from the value in control Purkinje fibers from noninfarcted preparations (-85.0 +/- 4.5 mV). The intracellular potassium ion activity was reduced by 50.4 mM during this time (intracellular potassium ion activity equals 61.6 +/- 16.1 mM, as compared to control intracellular potassium ion activity of 112 +/- 19.8 mM). The potassium equilibrium potential was reduced by 16.0 mV (from -97.2 +/- 4.7 mV in controls to -81.2 +/- 6.9 mV), thus accounting for about one half of the reduction in the maximum diastolic potential. After 6 hours of superfusion, the maximum diastolic potential increased to -78.9 +/- 8.7 mV (still significantly less than control). The potassium equilibrium potential had largely recovered (-93.8 +/- 5.9 mV). The intracellular sodium ion activity of Purkinje fibers in the infarcts (15.6 +/- 6.9 mM) was elevated during the first hour of superfusion by 6.2 mM compared to control (9.4 +/- 2.6 mM), and this was only 12% as much as the initial intracellular potassium ion activity decrease. Sodium ion activity after 3-6 hours of superfusion was not significantly different than normal (12.1 +/- 4.9 mM). In conclusion, only a portion of the maximum diastolic potential changes can be explained by a reduction of the potassium equilibrium potential. It is likely that change(s) in the cell membrane sodium-potassium pump's function and in the membrane conductance are also involved. Furthermore, the lack of a compensatory increase in intracellular sodium ion activity accompanying the large reduction of intracellular potassium ion activity may be a consequence of the cellular acidosis, which is known to occur during myocardial ischemia.

Changes in intra- and extracellular potassium and intracellular sodium activities induced by repetitive stimulation and their relation to membrane potential in guinea-pig papillary muscle.

We measured changes in membrane potential (MP), extra- and intracellular potassium and intracellular sodium ion activities (aKo, aKi, and aNai) in papillary muscle of the guinea-pig heart induced by repetitive stimulation at various frequencies and periods in vitro, using double-barrelled ion-selective microelectrodes. Stimulation (2-4 Hz) depolarized the cells, and termination of stimulation induced hyperpolarization. The aKi and aNai (stimulated at 0.2 Hz) were 92.3 +/- 4.6 and 7.8 +/- 2.0 mM (mean +/- S.D.), respectively. Prolongation of the stimulation period (0.5-2 min) increased aNai time-dependently, but there was no further increase by stimulation for longer than 3 min. The increase in aNai was dependent on stimulus frequency. After termination of the stimulation aiNa declined exponentially. aKi slightly decreased by the stimulation (3-4 Hz). aKo increased during the stimulation period, and decreased below the initial level after termination of the stimulation. Results suggest that in guinea-pig papillary muscle, the contribution of an electrogenic component of Na-K pump to the hyperpolarization after stimulation would be small, since the hyperpolarization could be explained mostly by depletion of aKo induced by Na-K pump activity.

O-145 - Effects of extracellular potassium and pH on intracellular sodium ion activity of guinea-pig cardiac muscle

O-145 - Effects of extracellular potassium and pH on intracellular sodium ion activity of guinea-pig cardiac muscle

The role of mucus in ion absorption by the oesophagus of the sea-water eel (Anguilla anguilla L.)

1. The structure of mucus in the oesophagus of the sea-water adapted eel, consists of a framework of fibers decreasing in density and thickness from the anterior to the posterior oesophagus. 2. With seawater in the lumen the mucus layer supports, in vitro, about 45% of the lumen to serosa gradient of sodium ion activity along the whole oesophagus. It supports different chloride ion activity gradients: about 80% in the anterior and about 45% in the middle and posterior oesophagus. These results are confirmed by X-ray micro-analysis. 3. Experiments without lumen-to-serosa gradients demonstrate a linked sodium and chloride active absorption appearing in the middle oesophagus and increasing towards the posterior oesophagus. 4. Na+−K+-ATPase is cytochemically demon-strated but could not be inhibited by ouabain during in vitro experiments, due to its particular localization.