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Open AccessJournal ArticleDOI

Inactivation of delayed outward current in molluscan neurone somata.

Richard W. Aldrich, +2 more
- 01 Jun 1979 - 
- Vol. 291, Iss: 1, pp 507-530
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TLDR
Inactivation of delayed outward current was studied by voltage clamp of isolated neurone somata of the molluscs Archidoris and Anisodoris and shows cumulative inactivation during repetitive voltage clamp pulses.
Abstract
1. Inactivation of delayed outward current was studied by voltage clamp of isolated neurone somata of the molluscs Archidoris and Anisodoris. During prolonged voltage clamp steps in normal artificial sea water delayed outward current rises to a peak and then declines to a non-zero steady-state. During repetitive clamp pulses at repetition rates slower than 2/sec, the amplitude of peak outward current in the second pulse is commonly less than the amplitude at the end of the preceding pulse, giving the impression of continued inactivation during the repolarized interval. We have termed this property cumulative inactivation. 2. Two components of delayed outward current were separated using tetraethyl ammonium ions (TEA) and cobalt ions (Co). External TEA blocks 90% of a voltage and time dependent outward current termed K current (IK). External Co blocks 85% of a Ca activated delayed outward current termed Ca current (ICa does not inactivate during prolonged or repetitive voltage clamp pulses. IK, however, inactivates during prolonged voltage clamp steps and shows cumulative inactivation during repetitive voltage clamp pulses. 3. Inactivation of IK is voltage and time dependent and does not require influx of Ca ions. 4. As measured by a prepulse method, the onset of inactivation is characterized by a two time constant process. Fast inactivation occurs with a time course comparable to the rate of rise of outward current and can account for 90% of total inactivation. 5. Recovery from inactivation is slow with a time constant approximately an order of magnitude slower than the onset of inactivation. 6. The current-voltage (I-V) curve for peak IK can be N-shaped, with a region of negative slope resistance in the range of +30 to +80 mV. The I-V curve for steady-state IK, however, shows little or no tendency to form a local maximum. 7. The pattern of delayed outward current varies considerably between cells. A major contributing factor to this variability appears to be the relative contributions of ICa and IK to delayed outward current.

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References
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Journal ArticleDOI

A quantitative description of membrane current and its application to conduction and excitation in nerve

TL;DR: This article concludes a series of papers concerned with the flow of electric current through the surface membrane of a giant nerve fibre by putting them into mathematical form and showing that they will account for conduction and excitation in quantitative terms.
Journal ArticleDOI

Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.

TL;DR: A number of compounds related to TEA+ (tetraethylammoniumion) were injected into squid axons and their effects on g K (the potassium conductance) were determined, suggesting that K+ ions traverse the membrane by way of pores, and they cannot be explained by the usual type of carrier model.
Journal ArticleDOI

Prediction of repetitive firing behaviour from voltage clamp data on an isolated neurone soma

TL;DR: Membrane parameters of an isolated neural cell body have been determined by voltage clamp analysis and data are expressed as membrane ion‐specific conductances, leak conductance, and capacitance.
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