The Inner Quaternary Ammonium Ion Receptor in Potassium Channels of the Node of Ranvier

Quaternary ammonium ions were applied to the inside of single myelinated nerve fibers by diffusion from a cut end. The resulting block of potassium channels in the node of Ranvier was studied under voltage-clamp conditions. The results agree in almost all respects with similar studies by Armstrong of squid giant axons. With tetraethylammonium ion (TEA), pentyltriethylammonium ion (C5), or nonyltriethylammonium ion (C9) inside the node, potassium current during a depolarization begins to rise at the normal rate, reaches a peak, and then falls again. This unusual inactivation is more complete with C9 than with TEA. Larger depolarizations give more block. Thus the block of potassium channels grows with time and voltage during a depolarization. The block reverses with repolarization, but for C9 full reversal takes seconds at -75 mv. The reversal is faster in 120 mM KCl Ringer's and slower during a hyperpolarization to -125 mv. All of these effects contrast with the time and voltage-independent block of potassium, channels seen with external quaternary ammonium ions on the node of Ranvier. External TEA, C5, and C9 block without inactivation. The external quaternary ammonium ion receptor appears to be distinct from the inner one. Apparently the inner quaternary ammonium ion receptor can be reached only when the activation gate for potassium channels is open. We suggest that the inner receptor lies within the channel and that the channel is a pore with its activation gate near the axoplasmic end.

[1]  B. Hille The Permeability of the Sodium Channel to Organic Cations in Myelinated Nerve , 1971, The Journal of general physiology.

[2]  C. Armstrong Interaction of Tetraethylammonium Ion Derivatives with the Potassium Channels of Giant Axons , 1971, The Journal of general physiology.

[3]  C M Armstrong,et al.  Inactivation of the Potassium Conductance and Related Phenomena Caused by Quaternary Ammonium Ion Injection in Squid Axons , 1969, The Journal of general physiology.

[4]  W. Vogel,et al.  Effects of tetrodotoxin and tetraethylammonium chloride on the inside of the nodal membrane ofXenopus laevis , 1969 .

[5]  B. Hille The Selective Inhibition of Delayed Potassium Currents in Nerve by Tetraethylammonium Ion , 1967, The Journal of general physiology.

[6]  C. Armstrong Time Course of TEA+-Induced Anomalous Rectification in Squid Giant Axons , 1966, The Journal of general physiology.

[7]  C. Armstrong,et al.  Anomalous Rectification in the Squid Giant Axon Injected with Tetraethylammonium Chloride , 1965, The Journal of general physiology.

[8]  B. Frankenhaeuser,et al.  A quantitative description of potassium currents in myelinated nerve fibres of Xenopus laevis , 1963, The Journal of physiology.

[9]  B. Frankenhaeuser,et al.  Instantaneous potassium currents in myelinated nerve fibres of Xenopus laevis , 1962, The Journal of physiology.

[10]  B. Frankenhaeuser,et al.  Quantitative description of sodium currents in myelinated nerve fibres of Xenopus laevis , 1960, The Journal of physiology.

[11]  F. Dodge,et al.  Membrane currents in isolated frog nerve fibre under voltage clamp conditions , 1958, The Journal of physiology.

[12]  Ichiji Tasaki,et al.  DEMONSTRATION OF TWO STABLE POTENTIAL STATES IN THE SQUID GIANT AXON UNDER TETRAETHYLAMMONIUM CHLORIDE , 1957, The Journal of general physiology.