» Articles » PMID: 6302670

Identification of Two Sodium Channel Subtypes in Chick Heart and Brain

Overview
Specialty Science
Date 1983 Feb 1
PMID 6302670
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Na+ channels in chick brain and heart have been directly compared by measuring binding of tritium-labeled saxitoxin ([3H]STX) to the two tissues under identical conditions. Maximum saturable uptake and toxin affinity were considerably less in chick heart than in chick brain, requiring the development of an assay method to resolve specific [3H]STX uptake in heart. With this method, binding to both preparations consisted of a specific saturable component and a linear nonspecific component. The equilibrium dissociation constant for [3H]STX measured in chick heart (6.2-8.8 nM) was 20-30 times higher than that measured in chick brain (0.3 nM). The dissociation rate for [3H]STX was only about twice as fast in heart as it was in brain, indicating that the decrease in toxin affinity in heart results predominantly from a slowed toxin association rate. The decreased affinity for [3H]STX found at the chick heart Na+ channel is compared with toxin-resistant Na+ channels in other preparations. The existence of two Na+ channel subtypes is proposed, with high affinity and low affinity for saxitoxin and tetrodotoxin; the significance of this classification is discussed.

Citing Articles

Axonal sodium channel NaV1.2 drives granule cell dendritic GABA release and rapid odor discrimination.

Nunes D, Kuner T PLoS Biol. 2018; 16(8):e2003816.

PMID: 30125271 PMC: 6117082. DOI: 10.1371/journal.pbio.2003816.


Voltage-gated sodium channels in the mammalian heart.

Zimmer T, Haufe V, Blechschmidt S Glob Cardiol Sci Pract. 2015; 2014(4):449-63.

PMID: 25780798 PMC: 4355518. DOI: 10.5339/gcsp.2014.58.


Tetrodotoxin sensitivity of the vertebrate cardiac Na+ current.

Vornanen M, Hassinen M, Haverinen J Mar Drugs. 2011; 9(11):2409-2422.

PMID: 22163193 PMC: 3229242. DOI: 10.3390/md9112409.


Structure, function and expression of voltage-dependent sodium channels.

Kallen R, Cohen S, Barchi R Mol Neurobiol. 1993; 7(3-4):383-428.

PMID: 8179845 DOI: 10.1007/BF02769184.


Identification of two calcium channel receptor sites for [3H]nitrendipine in mammalian cardiac and smooth muscle membrane.

Rogart R, deBruyn Kops A, Dzau V Proc Natl Acad Sci U S A. 1986; 83(19):7452-6.

PMID: 2429306 PMC: 386736. DOI: 10.1073/pnas.83.19.7452.


References
1.
Harris J, THESLEFF S . Studies on tetrodotoxin resistant action potentials in denervated skeletal muscle. Acta Physiol Scand. 1971; 83(3):382-8. DOI: 10.1111/j.1748-1716.1971.tb05091.x. View

2.
Catterall W . Inhibition of voltage-sensitive sodium channels in neuroblastoma cells by antiarrhythmic drugs. Mol Pharmacol. 1981; 20(2):356-62. View

3.
Reed J, RAFTERY M . Properties of the tetrodotoxin binding component in plasma membranes isolated from Electrophorus electricus. Biochemistry. 1976; 15(5):944-53. DOI: 10.1021/bi00650a002. View

4.
Baer M, Best P, Reuter H . Voltage-dependent action of tetrodotoxin in mammalian cardiac muscle. Nature. 1976; 263(5575):344-5. DOI: 10.1038/263344a0. View

5.
Ritchie J, Rogart R, Strichartz G . A new method for labelling saxitoxin and its binding to non-myelinated fibres of the rabbit vagus, lobster walking leg, and garfish olfactory nerves. J Physiol. 1976; 261(2):477-94. PMC: 1309152. DOI: 10.1113/jphysiol.1976.sp011569. View