Application of voltage clamp pulses to frog ventricular strips caused temporary changes in extracellular K concentration, with the N-shaped steady state current-voltage relation mainly reflecting K current voltage dependency.
Extracellular potassium accumulation in ventricular muscle
Voltage clamp pulses (1-10 sec)
Extracellular K concentration changes
Application of voltage clamp pulses (1--10 sec) to frog ventricular strips causes temporary changes in the extracellular K concentration. 2. The changes in the extracellular K concentration can be estimated from (a) slowly decaying post-clamp after-potentials, (b) changes in the action potential duration, and (c) measurements with a K-selective micro-electrode. 3. The depolarization of the resting potential and the shortening of the action potential are present in approximately the same proportions during voltage-clamp induced extracellular K accumulation and during perfusion with a K-ricn Ringer solution but small consistent differences are noticed. 4. The measurements of the after-potential, the action potential shortening, and the K-electrode response were analysed as indicators of extracellular K+ activity and it was concluded that the after-potential provides the most convenient and reliable estimate of the absolute magnitude of the voltage-clamp induced extracellular K accumulation. 5. The depolarizing after-potentials decay more slowly than the hyperpolarizing after-potentials but it is found that this reflects the selectivity of the membrane to K+ concentrations as predicted by the Nernst or the Goldman equations. 6. Analysis of the redistribution of accumulated K+ from the decay of the after-potential suggests that the major part of the redistribution process can be described by a single time constant (2--4 sec). A much longer time constant is required for a smaller component of the 'tail' in order to bring Ko to the normal resting state. 7. N-shaped relations similar to the 'steady state' current-voltage relation are obtained when the post-clamp after-potential, the action potential shortening, and the K-electrode response are plotted versus the clamped membrane potential. The maxima of these curves are located around -40 mV and the minima around -20 mV. 8. In spite of a significant outward membrane current (1--1.5 microamperemeter) in the minimum region (-20 mV), the post-clamp after-potential is often hyperpolarizing in nature suggesting extracellular K depletion. 9. These findings indicate that the K efflux is lower at -20 mV than at both higher and lower potentials and suggest that the N-shape 'steady state' current-voltage relation mainly reflects the voltage dependency of the K current. 10. A theory for K accumulation in a single compartment is presented which predicts that a simple linear RC-circuit may describe the electrical response of the preparation in a limited potential range around the resting potential. The extracellular accumulation space was estimated to be 13--16% of the total volume of the preparation. It is tentatively suggested that the accumulation space is equivalent to the subendothelial fraction of the extracellular space.
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Cleemann et al. (Mon,) conducted a other in Extracellular potassium accumulation in ventricular muscle. Voltage clamp pulses was evaluated on Extracellular K concentration changes. Application of voltage clamp pulses to frog ventricular strips caused temporary changes in extracellular K concentration, with the N-shaped steady state current-voltage relation mainly reflecting K current voltage dependency.
synapsesocial.com/papers/6a090a4e2757fd3263d3aa93 — DOI: https://doi.org/10.1113/jphysiol.1979.sp012608
Lars Nilausen Cleemann
Moesgaard Museum
Martin Morad
Electrophysiology
The Journal of Physiology
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