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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 26 (1976), S. 51-70 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary An increase in extracellular Ca concentration causes the membrane of giant red cells of the salamander,Amphiuma means, to undergo a marked, transient hyperpolarization. This hyperpolarization is caused by an increase in K permeability of the membrane as judged from the K sensitivity of the membrane potential and from the rate of K loss under influence of raised extracellular Ca concentration. At constant external pH, the induction of hyperpolarization by increased extracellular Ca has a relatively well-defined threshold concentration. Furthermore the phenomenon is of an “all or none” type with most of the cells having membrane potential values either in the normal range (about −15 mV) or in the range −40 to −70 mV. Shortly after suspension in Ringer's with 15mM Ca, most if not all of the individual cells are hyperpolarized. Upon continued exposure (5–20 min) to the higher Ca concentration the membrane potential returns to the normal value in a fashion compatible with an “all or none” response. The observed Ca effect is sensitive to the pH of the suspending medium. At pH 6.2 the response is absent whereas the hyperpolarization is markedly stronger at pH 8.2 than at pH 7.2. It is argued that a reliable transport number for K under influence of Ca cannot be estimated from the slope of membrane potentialvs. log (extracellular K concentration). This is probably related to the fact that the membrane potentials of the cells in the population do not stay constant in time. The above phenomenon is compared with the Ca-induced K permeability in poisoned human red cells or red cell ghosts. It is important to note that the cells employed in the present study are neither poisoned nor mechanically disrupted. This study emphasizes that the role of Ca in regulating cell membrane permeability to K seems to be a general feature.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Intracellular potentials were measured, using a piezoelectric electromechanical transducer to impale Ehrlich ascites tumor cells with capillary microelectrodes. In sodium Ringer's, the potential immediately after the penetration was −24±7 mV, and decayed to a stable value of about −8 mV within a few msec. The peak potentials disappeared in potassium Ringer's and reappeared immediately after resuspension in sodium. Ringer's, whereas the stable potentials were only slightly influenced by the change of medium. The peak potential is in good agreement with the Nernst potential for chloride. This is also the case when cell sodium and potassium have been changed by addition of ouabain. It is concluded that the peak potentials represent the membrane potential of the unperturbed cell, and that chloride is in electrochemical equilibrium across the cell membrane. The membrane potential of about −11 mV previously reported corresponds to the stable potential in this study, and is considered as a junction potential between damaged cells and their environment. Similar potential differences were recorded between a homogenate of cells and Ringer's. The apparent membrane resistance of Ehrlich cells was about 70 Ωcm2. This is two orders of magnitude less than the value calculated from36Cl fluxes, and may, in part, represent a leak in the cell membrane. For comparison, the influence of an eventual leak on measurements in red cells and mitochondria is discussed.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 18 (1974), S. 125-144 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The erythrocyte ofAmphiuma means was chosen as a model for elucidation of membrane properties of red cells because the large size of this cell permitted direct measurements of plasma membrane potential. In the 30-sec period following micropuncture and withdrawal of the electrode the plasma membrane reseals and hyperpolarizes to a value of about −50 mV. The hyperpolarization is followed by a gradual return to the unperturbed potential of −15 mV. The magnitude of the hyperpolarization is strongly reduced by an increase in extracellular K concentration and is therefore related to an increase in relative K permeability. The transference number for K is calculated to have a maximal value of about 0.6. However, it is not yet clear whether the hyperpolarization can be solely attributed to a rise in K permeability, or whether there is a concomitant decline in Cl permeability as well. The magnitude of the hyperpolarization is unaffected by the presence of either ouabain or oligomycin. Extracellular Ca is prerequisite to the observed hyperpolarization and presumably acts by permitting the membrane to seal, and having entered the cell during the leak period, causes an increase in the relative K permeability. This permeability change resembles the Ca-induced rise in K permeability seen in metabolically depleted human red cells and red cell ghosts. An important difference, however, is that theAmphiuma red cells used in the present study are neither poisoned nor metabolically depleted so that the Ca effect is not prevented by the presence of cellular ATP as seems to be the case in human erythrocytes. The transient nature of the hyperpolarization may be related to the active transport of Ca out of the cell.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    The journal of membrane biology 39 (1978), S. 27-48 
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Like most other red cells, the giant erythrocytes ofAmphiuma means possess a system for rapid exchange of chloride across the membrane. Also, there are indications that the net transport of chloride in these cells is slow. The size ofAmphiuma erythrocytes allows direct measurements of membrane potential with microelectrodes. The present work exploits the possibility that such measurements can be used to give a quantitative estimate of the chloride conductance (G Cl) of the Amphiuma red cell membrane. The membrane potential was measured as a function of extracellular chloride concentration (5–120mM), using an impermeant anion (Para-amino-hippurate) as a substitute. Furthermore, the effect of different pH values (6.0–7.2) was studied. For each extracellular chloride concentration the membrane potential was determined at a pH at which hydroxyl, hydrogen, and bicarbonate ions were in electrochemical equilibrium. From these membrane potentials and the corresponding chloride concentrations in the medium (at constant intracellular ion concentrations), theG Cl of the membrane was calculated to be 3.9×10−7 {ie27-1} cm−2. This value is some six orders of magnitude smaller than that calculated from the rate of tracer exchange under equilibrium conditions. The experimental strategy used gives the value for a “partial transference number” which takes into account only ions which arenot in electrochemical equilibrium. Whereas this approach gives a value forG Cl, it does not permit calculation of the overall membrane conductance. From the calculated value ofG Cl it is possible to estimate that the maximal value of the combined conductances of hydroxyl (or proton) and bicarbonate ions is 0.6×10−7 {ie27-2} cm−2. The large discrepancy between the rate of exchange of chloride and its conductance is in agreement with measurements on human and sheep red cells employing the ionophore valinomycin to increase the potassium conductance of the membrane. The results in the present study were, however, obtained without valinomycin and an accompanying assumption of a constant field in the membrane. Therefore, the present measurements give independent support to the above mentioned conclusions.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 406 (1975), S. 516-525 
    ISSN: 0005-2736
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 770 (1984), S. 1-6 
    ISSN: 0005-2736
    Keywords: (Erythrocyte membrane) ; Ca^2^+ dependence ; Calmodulin ; K^+ channel
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 448 (1976), S. 599-606 
    ISSN: 0005-2736
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Biochimica et Biophysica Acta (BBA)/Biomembranes 686 (1982), S. 225-232 
    ISSN: 0005-2736
    Keywords: (Erythrocyte) ; Fluorescent probe ; Ion effect ; Membrane potential
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Medicine , Physics
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 0550-3213
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0550-3213
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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