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Sodium Pump

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The following article is from The Great Soviet Encyclopedia (1979). It might be outdated or ideologically biased.

Sodium Pump

 

(or sodium-potassium pump), in biochemistry, a membrane mechanism that maintains a definite ratio of Na + and K + ions in cells by active transport of the ions against electrochemical and concentration gradients. The cells of most tissues contain more K + ions than Na + ions, whereas the fluids reaching the tissues (blood, lymph, and intercellular fluid) contain significantly higher concentrations of Na +. A certain number of ions continuously enters and leaves the cells. The passive transport of cations (transfer of ions through the membrane by means of a system of special channels along the electrochemical and concentration gradients) is, on the average, compensated by active ion transport.

The function of the sodium pump is related to the transfer of metabolites into the cells and, in the case of nerve and muscle fibers, is also related to the mechanism of excitation. The active transfer of Na + from the cell is associated with the transport of K + in the opposite direction and is accomplished by a special enzyme system, the sodium-potassium transport system, which is stimulated by adenosine triphosphatase localized in the cell membrane. By hydrolyzing adenosine triphosphate (ATP), adenosine triphosphatase liberates energy, which is expended on the active transfer of cations. The working of the sodium pump on the whole depends on the level of cell metabolism.

R. N. GLEBOV

The Great Soviet Encyclopedia, 3rd Edition (1970-1979). © 2010 The Gale Group, Inc. All rights reserved.
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References in periodicals archive
For example, when primary sodium pump trips, an operator expects flow of the coolant to stop.
Bovine adrenals contain in addition to ouabain, a second inhibitor of sodium pump. J Biol Chem 1998;273:784-92.
In general, animal cells routinely expend 20%-30% of their total metabolic energy on the activity of a single protein complex, the sodium pump ([Na.sup.+], [K.sup.+]-ATPase; Siems et al., 1982, 1992), and for adult marine invertebrates, the sodium pump can potentially account for 30%-70% of tissue metabolism (Baker and Connelly, 1966; Lucu and Pavicic, 1995).
Endogenous sodium pump inhibits and blood pressure regulation: an uptake on recent progress.
Endogenous mammalian cardenolides are thought to be effector ligands that regulate the sodium pump as a receptor.
The sodium is moved into the extracellular fluid by the sodium pump and diffuses out through the junction between the two chloride cells.
A mechanism for direct hormonal control of the sodium pump may play an important role
However, in recent studies using microgram amounts of purified material (5, 7), molecular mass and proton nuclear magnetic resonance ([sup.1]H NMR) [4] spectroscopic measurements have demonstrated that the adrenal and hypothalamic sodium pump inhibitors are indistinguishable from authentic ouabain.
The sodium pump [[Na.sup.+],[K.sup.+]-ATPase (NKA); [3] EC 3.6.1.37] is an integral membrane-anchored protein that couples the energy released in the enzymatic hydrolysis of ATP to the translocation of sodium and potassium ions across the cell membrane.
Depending on the experimental conditions used (e.g., [K.sup.+] concentration and type of membrane isolated), the affinity constant for binding of digoxin to its receptor (the sodium pump) has been reported to be in the range [10.sup.6]-[10.sup.8] L/mol (4, 5).
Sodium pump activity was estimated as ouabain-sensitive [sup.86]Rb uptake into human erythrocytes from healthy donors as previously described [12].
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