The diffusion and electrogenic components of the membrane potential of hypoxic myocardium

1987 ◽  
Vol 65 (2) ◽  
pp. 246-251 ◽  
Author(s):  
Normand Leblanc ◽  
Elena Ruiz-Ceretti
Keyword(s):  
Membrane Potential ◽  
Sodium Pump ◽  
Resting Potential ◽  
Krebs Solution ◽  
Ventricular Muscle ◽  
Diffusion Component ◽  
K Concentration ◽  
Zero Potential ◽  
K Permeability ◽  
External K

The diffusion and electrogenic components of the resting potential of hypoxic ventricular muscle were separated by inhibition of the sodium pump with 10−4 M ouabain. The response to varying external K concentrations (Ko) was studied. Arteriaily perfused rabbit hearts were submitted to 60 min hypoxia in Krebs solution containing 5 mM K throughout or to different external K concentrations during the last 20 min of hypoxia. For K concentrations between 1.5 and 10 mM, hypoxia did not change the resting potential except for a slight hyperpolarization in 7.5 mM K. The diffusion component of the resting potential did not differ from the resting potential at Ko < 5 mM. An electrogenic potential of −3 to −6 mV was detectable at Ko values between 5 and 10 mM. The internal K concentration, Ki, was estimated from extrapolations to zero potential of the relation resting potential vs. Ko in normoxic and hypoxic hearts. These experiments revealed a decline of Ki of 16 mM with hypoxia. The variation of the diffusion potential with external K was fitted by a PNa:PK ratio five times lower than in normoxia. It has been concluded that an increase in K permeability and the persistence of electrogenic Na extrusion during hypoxia of rather short duration prevent membrane depolarization despite the myocardial K loss.

Insulin and the resting potential of hypoxic substrate-deprived myocardium

1988 ◽  
Vol 66 (2) ◽  
pp. 202-206 ◽  
Author(s):  
Elena Ruiz-Ceretti ◽  
Fabien DeLorenzi ◽  
Josée S. Lafond ◽  
Denis Chartier
Keyword(s):  
Membrane Potential ◽  
Action Potential ◽  
Cardiac Glycosides ◽  
Sodium Pump ◽  
Ionic Transport ◽  
Resting Potential ◽  
Diffusion Component ◽  
Substrate Deprivation ◽  
Microelectrode Techniques ◽  
Action Potential Configuration

Insulin stimulates ionic transport by the sodium pump and induces hyperpolarization in skeletal and cardiac muscle among other cells. The insulin-induced hyperpolarization in most cases can be inhibited by exposure to cardiac glycosides or metabolic inhibition. However, extracellular accumulation of K ions leaking from hypoxic cells in superfused preparations may distort the effects of insulin on the resting potential. We used standard microelectrode techniques and perfused rabbit hearts submitted to hypoxia and substrate deprivation to reinvestigate the effects of insulin (6.4 nM) on the membrane potential. The membrane depolarized by about 6 mV and the action potential was reduced to a sharp spike without overshoot. Insulin restored the resting potential to control values but did not change the action potential configuration substantially. The insulin-induced repolarization was not due to reuptake of potassium as revealed by spectrophotometric determinations of myocardial K content. In addition, the diffusion component of the resting potential measured after inhibition of the sodium pump with 10−4 M ouabain was not modified by insulin. Our results suggest that an increase in the contribution of electrogenic Na extrusion to the resting potential underlies the repolarizing effect of insulin of hypoxic substrate-deprived myocardium.

scholarly journals Effect of acetylcholine on postjunctional membrane permeability in eel electroplaque.

1977 ◽  
Vol 70 (1) ◽  
pp. 23-36 ◽  
Author(s):  
N L Lassignal ◽  
A R Martin
Keyword(s):  
Field Equation ◽  
Membrane Potential ◽  
Membrane Permeability ◽  
Ionic Composition ◽  
Reversal Potential ◽  
Resting Potential ◽  
Constant Field ◽  
Free Solution ◽  
Positive Direction ◽  
External K

Acetylcholine (ACh) was applied iontophoretically to the innervated face of isolated eel electroplaques while the membrane potential was being recorded intracellularly. At the resting potential (about -85 mV) application of the drug produced depolarizations (ACh potentials) of 20 mV or more which became smaller when the membrane was depolarized and reversed in polarity at about zero membrane potential. The reversal potential shifted in the negative direction when external Na+ was partially replaced by glucosamine. Increasing external K+ caused a shift of reversal potential in the positive direction. It was concluded that ACh increased the permeability of the postjunctional membrane to both ions. Replacement of Cl- by propionate had no effect on the reversal potential. In Na+-free solution containing glucosamine the reversal potential was positive to the resting potential, suggesting that ACh increased the permeability to glucosamine. Addition of Ca++ resulted in a still more positive reversal potential, indicating an increased permeability to Ca++ as well. Analysis of the results indicated that the increases in permeability of the postjunctional membrane to K+, Na+, Ca++, and glucosamine were in the ratios of approximately 1.0:0.9:0.7:0.2, respectively. With these permeability ratios, all of the observed shifts in reversal potential with changes in external ionic composition were predicted accurately by the constant field equation.

scholarly journals Strophanthidin-sensitive sodium fluxes in metabolically poisoned frog skeletal muscle.

1976 ◽  
Vol 68 (4) ◽  
pp. 405-420 ◽  
Author(s):  
B G Kennedy ◽  
P De Weer
Keyword(s):  
Skeletal Muscle ◽  
Membrane Potential ◽  
Human Erythrocyte ◽  
Sodium Pump ◽  
Giant Axon ◽  
Squid Giant Axon ◽  
Frog Skeletal Muscle ◽  
Na Efflux ◽  
Unidirectional Fluxes ◽  
External K

Strophanthidin-sensitive and insensitive unidirectional fluxes of Na were measured in fog sartorius muscles whose internal Na levels were elevated by overnight storage in the cold. ATP levels were lowered, and ADP levels raised, by metabolic poisoning with either 2,4-dinitrofluorobenzene or iodoacetamide. Strophanthidin-sensitive Na efflux and influx both increased after poisoning, while strophanthidin-insensitives fluxes did not. The increase in efflux did not require the presence of external K but was greatly attenuated when Li replaced Na as the major external cation. Membrane potential was not markedly altered by 2,4-dinitrofluorobenzene. These observations indicate that the sodium pump of frog skeletal muscle resembles that of squid giant axon and human erythrocyte in its ability to catalyze Na-Na exchange to an extent determined by intracellular ATP/ADP levels.

Comparison of the electrical properties of arterial smooth muscle in normotensive rats and rats with deoxycorticosterone acetate-salt-induced hypertension: Possible involvement of (Na+-K+-Cl−) co-transport

1991 ◽  
Vol 81 (1) ◽  
pp. 73-78 ◽  
Author(s):  
J. P. L. Davis ◽  
A. R. Chipperfield ◽  
A. A. Harper
Keyword(s):  
Smooth Muscle ◽  
Membrane Potential ◽  
Vascular Smooth Muscle ◽  
Sprague Dawley ◽  
Deoxycorticosterone Acetate ◽  
Acetate Salt ◽  
Na Permeability ◽  
K Concentration ◽  
K Permeability

1. Hypertension was induced in male Sprague-Dawley rats by left unilateral nephrectomy and deoxycorticosterone acetate-salt administration. After 5 weeks, arterial systolic blood pressure was significantly elevated in these animals (191.5 ± 6.0 mmHg, mean ± sd, n = 17) compared with age-matched, unoperated control animals (134.0 ± 4.2 mmHg, n = 8, P < 0.001). 2. The membrane potential of femoral artery vascular smooth muscle measured in vitro was −55.1 ± 6.3 mV (mean ± sd, n = 154) for normotensive and −50.8 ± 5.7 mV (n = 82) for hypertensive animals. The difference in membrane potential was significant (P < 0.001). 3. The relationship between the log of the extracellular K+ concentration and membrane potential was nonlinear over the extracellular K+ concentration range 2.5–20 mmol/l, and showed a small positive shift with hypertension. 4. Tenfold reductions in the extracellular concentrations of Na+ or Cl− resulted in a membrane potential hyperpolarization in vascular smooth muscle from normotensive animals (4.9 ± 2.0 mV, n = 13 and 12.1 ± 1.3 mV, mean ± sd, n = 14, respectively). In vascular smooth muscle from hypertensive animals, the hyperpolarization in low-Na+ media was significantly increased to 12.2 ± 2.6 mV (mean ± sd, n = 5), but that in low-Cl− media was unaffected (2.7 ± 1.6 mV, n = 6). 5. The loop diuretic, bumetanide (10 μmol/l), hyperpolarized the membrane potential in vascular smooth muscle from both normotensive and hypertensive rats, but not in low-Na+ or low-Cl− media. This effect was significantly increased in hypertension, from 1.8 ± 0.7 mV (mean ± sd, n = 8) to 4.0 ± 1.0 mV (n = 5). 6. These results suggest that in these cells, K+ permeability ≫ Na+ permeability > Cl− permeabilty, and that the membrane potential is determined principally by the K+ permeability. In deoxycorticosterone acetate-salt hypertension, the membrane potential is depolarized, Na+ permeability is substantially increased, and there appears to be an increase in the activity of the (Na+-K+-Cl−) co-transporter.

scholarly journals Cat Heart Muscle in Vitro

1962 ◽  
Vol 46 (2) ◽  
pp. 189-199 ◽  
Author(s):  
Ernest Page
Keyword(s):  
Steady State ◽  
Heart Muscle ◽  
Potential Difference ◽  
Resting Potential ◽  
Equilibrium Potential ◽  
Papillary Muscles ◽  
K Concentration ◽  
Cat Heart ◽  
External K

The steady state transmembrane resting potential difference (Vm) has been measured in quiescent papillary muscles. Vm was determined as a function of the external K concentration in Cl and SO4 solutions and compared with the K equilibrium potential. Other measurements were made after replacement of external Na by choline, K by Rb and Cs, and Cl by SO4, CH3SO4, and NO3. Effects on Vm of albumin, temperature, and variation in internal K concentration are described.

scholarly journals The influence of external sodium ions on the sodium pump in erythrocytes

1968 ◽  
Vol 109 (3) ◽  
pp. 369-374 ◽  
Author(s):  
R. N. Priestland ◽  
R. Whittam
Keyword(s):  
Adenosine Triphosphatase ◽  
Sodium Pump ◽  
Erythrocyte Membranes ◽  
Sodium Ions ◽  
Adenosine Triphosphatase Activity ◽  
Sensitive Site ◽  
Na Efflux ◽  
Ion Movements ◽  
K Concentration ◽  
External K

1. A study has been made of the interaction between Na+ and K+ on the adenosine triphosphatase activity of erythrocyte ‘ghosts’, and on the K+ influx and Na+ efflux of intact erythrocytes. The adenosine triphosphatase activity and the ion movements were greater at a low external K+ concentration in the absence of Na+ than they were in the presence of 150mm-Na+. The inhibition by external Na+ of K+ influx had an inhibitory constant of 5–10mm. 2. Activation by K+ of kidney microsomal adenosine triphosphatase was retarded by Na+, and activation by Na+ was retarded by K+. Fragmented erythrocyte membranes behaved similarly. 3. These observations suggest that there is competition between Na+ and K+ at the K+-sensitive site of the membrane.

Hyperpolarization of mammalian skeletal muscle fibers in K-free media

1982 ◽  
Vol 242 (1) ◽  
pp. C12-C18 ◽  
Author(s):  
N. Akaike
Keyword(s):  
Time Course ◽  
Muscle Fibers ◽  
Resting Potential ◽  
Mammalian Skeletal Muscle ◽  
Krebs Solution ◽  
Free Medium ◽  
Metabolic Potential ◽  
Rat Soleus Muscle ◽  
K Concentration ◽  
Free Media

Time course of changes in resting potential following removal of K ions from Krebs solution was studied in the isolated rat soleus muscle. In K+-free Krebs solution the muscle fibers hyperpolarized to a peak within 60 min followed by a variable, gradual depolarization over the next few hours. A significant decrease of the intracellular K+ concentration ([K]i) occurred within 30 min in K+-free Krebs. Compensatory increase of the intracellular Na+ concentration ([Na]i) lagged behind [K]i change. Both hyperpolarization and successive depolarization were modified in K+-free medium containing different [Na]o, [Ca]o, or osmotic strength. A part of the hyperpolarization was reduced by adding ouabain. Therefore, ouabain-sensitive potential of the fibers in K+-free medium was attributed to the activation of electrogenic Na pump by K+ leaked out continuously from the fibers and accumulated just outside of cell membranes but not to changes of membrane Na+ and Cl- permeabilities. It is concluded that hyperpolarization of muscles exposed to K+-free medium is the sum of the diffusional K+ potential and ouabain-sensitive metabolic potential. Interestingly, the time course of changes of membrane response to K+-free krebs was identical for contralateral soleus muscles in the same rat, though it varied among different rats.

Measurements of the Intracellular Potassium Activity of Retzius Cells in the Leech Central Nervous System

1981 ◽  
Vol 91 (1) ◽  
pp. 87-101
Author(s):  
JOACHIM W. DEITMER ◽  
WOLF R. SCHLUE
Keyword(s):  
Cell Membrane ◽  
External Solution ◽  
Equilibrium Potential ◽  
The Mean ◽  
K Concentration ◽  
Retzius Cells ◽  
Intracellular K Activity ◽  
K Permeability ◽  
K Activity ◽  
External K

The intracellular K activity of leech Retzius cells was measured using double-barrelled, liquid ion exchanger, microelectrodes. At the normal external K+ concentration of 4 mm (equivalent to 3 mm-K activity, assuming an activity coefficient of 0.75) the mean K activity was 101.3 ± 7.6 mm (S.D., n = 14) in the cell bodies, and 4.35 ± 0.4 mV (n = 27) in the extracellular spaces surrounding them, indicating a K+ equilibrium potential of - 80 mV. The mean membrane potential was - 43.6 + 4.9 mV (n = 14). In a K-free external solution, or in the presence of 5 × 10−4m-ouabain, the intracellular K activity decreased by up to 14 mm min−1. This indicates an efflux of K+ ions across the cell membrane of approximately 2 × 10−10 mol cm−2s, and an apparent K+ permeability coefficient of 8 × 10−8 cms−1. The cell membrane depolarized upon removal of K+ and upon addition of ouabain, and transiently hyperpolarized beyond its initial level on return to the normal external K+ concentration. The recovery from this hyperpolarization paralleled the increase of the intracellular K activity following the re-addition of K+. Our results suggest that, despite the high K+ permeability of the Retzius cell membrane, the intracellular K activity is maintained at a high level by an electrogenic pump.

Interactions of membrane potential and cations in regulation of ciliary activity in Paramecium

1976 ◽  
Vol 65 (2) ◽  
pp. 427-448
Author(s):  
H. Machemer
Keyword(s):  
Membrane Potential ◽  
High Frequency ◽  
Resting Potential ◽  
Ciliary Activity ◽  
Frequency Increase ◽  
External Concentration ◽  
Membrane Hyperpolarization ◽  
Ciliary Beating ◽  
Fixed Membrane ◽  
K Concentration

Ciliary activity in Paramecium was investigated in different external solutions using techniques of voltage clamp and high frequency cinematography. An increase in the external concentration of K, Ca or Mg ions decreased the resting potential. It had no effect on ciliary activity. When the membrane potential was fixed, an increase in external Ca or Mg and, to a lesser extent, an increase in K concentration, raised the frequency of normal beating or decreased the frequency of reversed beating of the cilia. Similar effects resulted from membrane hyperpolarization with constant ionic conditions. Increase in concentration of Ca, but not of Mg or K, enhanced hyperpolarization-induced augmentation of ciliary frequency. Increase in Ca concentration also specifically augmented the delayed increase in inward current during rapid hyperpolarizing clamp. The results support the view that [Ca]i regulates the frequency and direction of ciliary beating. It is suggested that the insensitivity of the ciliary motor system to elevations of the external concentrations of ions results from compensation of their effects on [Ca]i. Depolarization itself appears to increase [Ca]i while elevation of the external ion concentrations at a fixed membrane potential appears to decrease [Ca]i.

Nombres de Transport, tK, tNa et tca Pour la Membrane de la Cellule Hépatique In Vivo

1972 ◽  
Vol 50 (5) ◽  
pp. 416-422 ◽  
Author(s):  
Jean Pierre Caillé ◽  
O. F. Schanne
Keyword(s):  
Membrane Potential ◽  
Liver Cell ◽  
Ionic Mobility ◽  
Irreversible Thermodynamics ◽  
Transport Numbers ◽  
Experimental Conditions ◽  
External Potassium ◽  
K Concentration ◽  
External K

We measured the membrane potential of the liver cell in vivo at 38 °C as we increased the external potassium. For the range of K concentration from 20.4 to 78 mM, the membrane potential of the liver cell decreased with a slope of 20.2 mV per decade change in external K concentration. The tissue content of K, Na, and Cl was analyzed under the same experimental conditions. The cytoplasmic resistivity (111 ± 17.5 Ω-cm) was used as a criterion for the state of the ions in the cytoplasm. This result, when it is compared with the value predicted from the ionic content, suggests that either the ionic mobility or the ionic activity in the cytoplasm of the liver cell is less than in a simple salt solution. An analytical expression, derived with the use of irreversible thermodynamics, permits us to calculate the transport numbers for the ions K, Na, and Cl in the membrane of the liver cell (tK 0.28, tNa 0.12, tCl 0.61).

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