» Articles » PMID: 2446906

Contribution of the Na+/K+-pump to the Membrane Potential

Overview
Journal Experientia
Specialty Science
Date 1987 Dec 1
PMID 2446906
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The inward movement of sodium ions and the outward movement of potassium ions are passive and the reverse movements against the electrochemical gradients require the activity of a metabolism-driven Na+/K+-pump. The activity of the Na+/K+-pump influences the membrane potential directly and indirectly. Thus, the maintenance of a normal electrical function requires that the Na+/K+-pump maintain normal ionic concentrations within the cell. The activity of the Na+/K+-pump also influences the membrane potential directly by generating an outward sodium current that is larger when the Na+/K+-pump activity is greater. The activity of the Na+/K+-pump is regulated by several factors including the intracellular sodium concentration and the neuromediators norepinephrine and acetylcholine. The inhibition of the Na+/K+-pump can lead indirectly to the development of inward currents that may cause repetitive activity. Therefore, the Na+/K+-pump modifies the membrane potential in different ways both under normal and abnormal conditions and influences in an essential way many cardiac functions, including automaticity, conduction and contraction. Key words. Active transport of ions; cardiac tissues; electroneutral and electrogenic Na+/K/-pump; control of Na+/K+-pump; normal and abnormal electrical events.

Citing Articles

The endoplasmic reticulum plays a key role in α-cell intracellular Ca dynamics and glucose-regulated glucagon secretion in mouse islets.

Acreman S, Ma J, Denwood G, Gao R, Tarasov A, Rorsman P iScience. 2024; 27(5):109665.

PMID: 38646167 PMC: 11033163. DOI: 10.1016/j.isci.2024.109665.


Mechanisms underlying pathological cortical bursts during metabolic depletion.

Dutta S, Iyer K, Vanhatalo S, Breakspear M, Roberts J Nat Commun. 2023; 14(1):4792.

PMID: 37553358 PMC: 10409751. DOI: 10.1038/s41467-023-40437-0.


Physiological Effects of the Electrogenic Current Generated by the Na/K Pump in Mammalian Articular Chondrocytes.

Maleckar M, Martin-Vasallo P, Giles W, Mobasheri A Bioelectricity. 2021; 2(3):258-268.

PMID: 34471850 PMC: 8370340. DOI: 10.1089/bioe.2020.0036.


Cannabidiol and Sodium Channel Pharmacology: General Overview, Mechanism, and Clinical Implications.

Ghovanloo M, Ruben P Neuroscientist. 2021; 28(4):318-334.

PMID: 34027742 PMC: 9344566. DOI: 10.1177/10738584211017009.


A functional interaction between GRP78 and Zika virus E protein.

Khongwichit S, Sornjai W, Jitobaom K, Greenwood M, Greenwood M, Hitakarun A Sci Rep. 2021; 11(1):393.

PMID: 33432092 PMC: 7801745. DOI: 10.1038/s41598-020-79803-z.


References
1.
Deitmer J, Ellis D . Interactions between the regulation of the intracellular pH and sodium activity of sheep cardiac Purkinje fibres. J Physiol. 1980; 304:471-88. PMC: 1282943. DOI: 10.1113/jphysiol.1980.sp013337. View

2.
Polimeni P, Vassalle M . On the mechanism of ouabain toxicity in Purkinje and ventricular muscle fibers at rest and during activity. Am J Cardiol. 1971; 27(6):622-9. DOI: 10.1016/0002-9149(71)90226-8. View

3.
Kass R, Lederer W, Tsien R, Weingart R . Role of calcium ions in transient inward currents and aftercontractions induced by strophanthidin in cardiac Purkinje fibres. J Physiol. 1978; 281:187-208. PMC: 1282691. DOI: 10.1113/jphysiol.1978.sp012416. View

4.
Weidmann S . Effects of calcium ions and local anesthetics on electrical properties of Purkinje fibres. J Physiol. 1955; 129(3):568-82. PMC: 1365985. DOI: 10.1113/jphysiol.1955.sp005379. View

5.
Vassalle M, VAGNINI F, GOURIN A, STUCKEY J . Suppression and initiation of idioventricular automaticity during vagal stimulation. Am J Physiol. 1967; 212(1):1-7. DOI: 10.1152/ajplegacy.1967.212.1.1. View