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Tetrodotoxin block of sodium channels in rabbit Purkinje fibers. Interactions between toxin binding and channel gating.

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TLDR
Tetrodotoxin block of cardiac sodium channels was studied in rabbit Purkinje fibers using a two-microelectrode voltage clamp to measure sodium current andKinetically, TTX resembles local anesthetics, but its affinity remains unchanged during maintained depolarization.
Abstract
Tetrodotoxin (TTX) block of cardiac sodium channels was studied in rabbit Purkinje fibers using a two-microelectrode voltage clamp to measure sodium current. INa decreases with TTX as if one toxin molecule blocks one channel with a dissociation constant KD approximately equal to 1 microM. KD remains unchanged when INa is partially inactivated by steady depolarization. Thus, TTX binding and channel inactivation are independent at equilibrium. Interactions between toxin binding and gating were revealed, however, by kinetic behavior that depends on rates of equilibration. For example, frequent suprathreshold pulses produce extra use-dependent block beyond the tonic block seen with widely spaced stimuli. Such lingering aftereffects of depolarization were characterized by double-pulse experiments. The extra block decays slowly enough (tau approximately equal to 5 s) to be easily separated from normal recovery from inactivation (tau less than 0.2 s at 18 degrees C). The amount of extra block increases to a saturating level with conditioning depolarizations that produce inactivation without detectable activation. Stronger depolarizations that clearly open channels give the same final level of extra block, but its development includes a fast phase whose voltage- and time-dependence resemble channel activation. Thus, TTX block and channel gating are not independent, as believed for nerve. Kinetically, TTX resembles local anesthetics, but its affinity remains unchanged during maintained depolarization. On this last point, comparison of our INa results and earlier upstroke velocity (Vmax) measurements illustrates how much these approaches can differ.

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Early afterdepolarizations: mechanism of induction and block. A role for L-type Ca2+ current.

TL;DR: The results support a hypothesis that the induction of EADs near action potential plateau voltages requires a conditioning phase controlled by the sum of membrane currents present near theaction potential plateau and characterized by lengthening and flattening of the plateau within a voltage range where recovery from inactivation and reactivation of L-type Ca2+channels to carry the depolarizing charge can occur.
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Primary structure and functional expression of the human cardiac tetrodotoxin-insensitive voltage-dependent sodium channel

TL;DR: The principal voltage-sensitive sodium channel from human heart has been cloned, sequenced, and functionally expressed and exhibits rapid activation and inactivation kinetics similar to native cardiac sodium channels.
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Lidocaine block of cardiac sodium channels.

TL;DR: Results provide direct evidence for the “modulated-receptor hypothesis” of Hille ( 1977) and Hondeghem and Katzung (1977) and argue that use dependence at therapeutic levels reflects block of inactivated channels, rather than block of open channels.
References
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Journal ArticleDOI

Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.

TL;DR: The results are interpreted in terms of a single receptor in Na channels for the different drug types, and any drug form in the channel increases the probability of closing the inactivation gate which, in effect, is equivalent to a negative shift of the voltage dependence of inactivation.
Journal ArticleDOI

The dual effect of membrane potential on sodium conductance in the giant axon of Loligo

TL;DR: This paper contains a further account of the electrical properties of the giant axon of Loligo and deals with the 'inactivation' process which gradually reduces sodium permeability after it has undergone the initial rise associated with depolarization.
Journal ArticleDOI

Inactivation of the sodium channel. I. Sodium current experiments.

TL;DR: This work interprets the correlations between inactivation and immobilization to mean that the immobilized charge returns slowly to "off" position with the time course of recovery from inactivation, and that the small current generated is lost in base-line noise.
Book

Electrophysiology of the heart

TL;DR: This has been a popular book, which covers the field of symptomatology in a remarkably complete way, in 32 short chapters, and the style is informal, almost chatty, but engaging.
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