Literature DB >> 2424514

A quantitative description of QX222 blockade of sodium channels in squid axons.

C F Starmer, J Z Yeh, J Tanguy.   

Abstract

The interaction of QX222, a quaternary ammonium derivative of lidocaine, with the Na channel was studied in internally perfused squid axons under voltage-clamped conditions. A use-dependent block was observed in response to repetitive depolarizing pulses. The time constant for block development and the steady state level of the block were increased with increasing frequency of stimulation from 0.1 to 10 Hz. Use-dependent block can be viewed as a net increase in the drug incorporation into Na channels with successive pulses. That is, net drug uptake by Na channels occurs during the depolarizing phase and net drug release occurs during the interpulse interval. The observed uptake rate of use-dependent block is shown to be a linear combination of the uptake rates associated with the depolarizing and resting potentials. Also, the steady state fraction of blocked channels is shown to be a linear combination of the state-dependent blockade equilibria. Drug-channel interactions are assumed to be dependent on gated control of the diffusion path between drug pool and the interior channel binding site. Drug ingress to the binding site can be inhibited by the channel gates (receptor guarding), while drug bound to the channel may become trapped by closure of the channel gates (trapping). On the basis of these assumptions, a simple procedure is proposed for estimating apparent rate constants governing the drug-channel binding reactions for two cases of channel blockade. The estimated forward (k) and backward (1) rate constants are: 2.45 x I05 M-1 s- and 0.23 x 103 s-1, respectively, for k and I for the case when the drug is trapped by both activation and inactivation gates, and 3.58 x 105 M-l s-l and 4.15 x 10-3 S-l for the case when the drug is not trapped. While these two schemes make a similar prediction with respect to the resulting uptake rates, their prediction of the steady state level of block differs. The observed steady state level of block could quantitatively be predicted by the trapped scheme but not by the untrapped scheme, thus providing a means for discriminating between these two schemes. In addition, the trapped scheme, but not the untrapped scheme, could provide an explanation for the observed voltage dependence of the slow recovery from use-dependent block.

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Year:  1986        PMID: 2424514      PMCID: PMC1329542          DOI: 10.1016/S0006-3495(86)83719-5

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  26 in total

1.  Mechanisms of use-dependent block of sodium channels in excitable membranes by local anesthetics.

Authors:  C F Starmer; A O Grant; H C Strauss
Journal:  Biophys J       Date:  1984-07       Impact factor: 4.033

2.  A pharmacological approach to the structure of the Na channel in squid axon.

Authors:  J Z Yeh
Journal:  Prog Clin Biol Res       Date:  1982

3.  The rates of interaction of local anesthetics with sodium channels in nerve.

Authors:  K R Courtney; J J Kendig; E N Cohen
Journal:  J Pharmacol Exp Ther       Date:  1978-11       Impact factor: 4.030

4.  Blockage of squid axon potassium conductance by internal tetra-N-alkylammonium ions of various sizes.

Authors:  R J French; J J Shoukimas
Journal:  Biophys J       Date:  1981-05       Impact factor: 4.033

5.  Block of sodium conductance and gating current in squid giant axons poisoned with quaternary strychnine.

Authors:  M D Cahalan; W Almers
Journal:  Biophys J       Date:  1979-07       Impact factor: 4.033

6.  Structure-activity relations for frequency-dependent sodium channel block in nerve by local anesthetics.

Authors:  K R Courtney
Journal:  J Pharmacol Exp Ther       Date:  1980-04       Impact factor: 4.030

7.  Local anesthetic block of sodium channels in normal and pronase-treated squid giant axons.

Authors:  M D Cahalan
Journal:  Biophys J       Date:  1978-08       Impact factor: 4.033

8.  Some kinetic and steady-state properties of sodium channels after removal of inactivation.

Authors:  G S Oxford
Journal:  J Gen Physiol       Date:  1981-01       Impact factor: 4.086

9.  Dynamics of 9-aminoacridine block of sodium channels in squid axons.

Authors:  J Z Yeh
Journal:  J Gen Physiol       Date:  1979-01       Impact factor: 4.086

10.  Inactivation of potassium current in squid axon by a variety of quaternary ammonium ions.

Authors:  R P Swenson
Journal:  J Gen Physiol       Date:  1981-03       Impact factor: 4.086

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  14 in total

1.  Temperature dependence of drug blockade of a calcium-dependent potassium channel in cultured hippocampal neurons.

Authors:  J G McLarnon; X P Wang
Journal:  Biophys J       Date:  1991-11       Impact factor: 4.033

2.  External Ba2+ block of human Kv1.5 at neutral and acidic pH: evidence for Ho+-induced constriction of the outer pore mouth at rest.

Authors:  Y May Cheng; David Fedida; Steven J Kehl
Journal:  Biophys J       Date:  2008-07-25       Impact factor: 4.033

3.  Characterization of concentration- and use-dependent effects of quinidine from conduction delay and declining conduction velocity in canine Purkinje fibers.

Authors:  D L Packer; A O Grant; H C Strauss; C F Starmer
Journal:  J Clin Invest       Date:  1989-06       Impact factor: 14.808

4.  The activation gate of the sodium channel controls blockade and deblockade by disopyramide in rabbit Purkinje fibres.

Authors:  R Gruber; E Carmeliet
Journal:  Br J Pharmacol       Date:  1989-05       Impact factor: 8.739

5.  Modelling frequency- and voltage-dependent effects of a class I antiarrhythmic drug (nicainoprol) on Vmax of the cardiac action potential from guinea-pig papillary muscle.

Authors:  J Weirich; H Antoni
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-10       Impact factor: 3.000

6.  Theoretical characterization of ion channel blockade. Competitive binding to periodically accessible receptors.

Authors:  C F Starmer
Journal:  Biophys J       Date:  1987-09       Impact factor: 4.033

7.  Molecular determinants of drug access to the receptor site for antiarrhythmic drugs in the cardiac Na+ channel.

Authors:  Y Qu; J Rogers; T Tanada; T Scheuer; W A Catterall
Journal:  Proc Natl Acad Sci U S A       Date:  1995-12-05       Impact factor: 11.205

8.  Mechanism of memantine block of NMDA-activated channels in rat retinal ganglion cells: uncompetitive antagonism.

Authors:  H S Chen; S A Lipton
Journal:  J Physiol       Date:  1997-02-15       Impact factor: 5.182

9.  Characterization of cocaine-induced block of cardiac sodium channels.

Authors:  W J Crumb; C W Clarkson
Journal:  Biophys J       Date:  1990-03       Impact factor: 4.033

10.  Prolonged sensory-selective nerve blockade.

Authors:  Itay Sagie; Daniel S Kohane
Journal:  Proc Natl Acad Sci U S A       Date:  2010-02-04       Impact factor: 11.205

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