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Membrane potential, single cells

Membrane Potentials Ion-selective electrodes, such as the glass pH electrode, function by using a membrane that reacts selectively with a single ion. figure 11.10 shows a generic diagram for a potentiometric electrochemical cell equipped with an ion-selective electrode. The shorthand notation for this cell is... [Pg.475]

Figure 1 Schematic diagrams illustrating the patch-clamp technique. (A) Overall setup for isolating single ionic channels in an intact patch of cell membrane. P = patch pipet R = reference microelectrode I = intracellular microelectrode Vp = applied patch potential Em = membrane potential Vm = Em — Vp = potential across the patch A = patch-clamp amplifier. (From Ref. 90.) (B) Five different recording configurations, and procedures used to establish them, (i) Cell attached or intact patch (ii) open cell attached patch (iii) whole cell recording (iv) excised outside-out patch (v) excised inside-out patch. Key i = inside of the cell o = outside of the cell. (Adapted from Ref. 283.)... Figure 1 Schematic diagrams illustrating the patch-clamp technique. (A) Overall setup for isolating single ionic channels in an intact patch of cell membrane. P = patch pipet R = reference microelectrode I = intracellular microelectrode Vp = applied patch potential Em = membrane potential Vm = Em — Vp = potential across the patch A = patch-clamp amplifier. (From Ref. 90.) (B) Five different recording configurations, and procedures used to establish them, (i) Cell attached or intact patch (ii) open cell attached patch (iii) whole cell recording (iv) excised outside-out patch (v) excised inside-out patch. Key i = inside of the cell o = outside of the cell. (Adapted from Ref. 283.)...
Fig. 21.2. Two-microelectrode current-clamp technique used to observe, in single Ascaris body muscle cells in a body-flap preparation, the response to a controlled pulsed application of levamisole. One micropipette, to measure membrane potential, and another micropipette, to inject current, are inserted inside the area of the muscle cell known as the bag region. Levamisole is applied in a time- and pressure-controlled manner from a microcatheter placed over the bag region of the muscle. A second microcatheter is used to apply additional chemical agents (Martin, 1982). Fig. 21.2. Two-microelectrode current-clamp technique used to observe, in single Ascaris body muscle cells in a body-flap preparation, the response to a controlled pulsed application of levamisole. One micropipette, to measure membrane potential, and another micropipette, to inject current, are inserted inside the area of the muscle cell known as the bag region. Levamisole is applied in a time- and pressure-controlled manner from a microcatheter placed over the bag region of the muscle. A second microcatheter is used to apply additional chemical agents (Martin, 1982).
Bolton But these are single cells, they are not resting. If you look at the membrane potentials they are very likely to be active. If you don t voltage clamp them, they can be spontaneously active. [Pg.172]

When a simple ISM is used in a single cell, the simplest arrangement involves placing a reference electrode outside the cell and the measured electromotive voltage must be corrected for the membrane potential. The latter is measured using a micropipette inserted inside the cell and connected to another reference electrode. However, this procedure is unsatisfactory for excitable cells, inside which an electrical field is formed. Double-barrelled ISMs (fig. 4.7), introduced... [Pg.73]


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See also in sourсe #XX -- [ Pg.2 , Pg.402 ]




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