Literature DB >> 15138746

Effect of extracellular pH on presteady-state and steady-state current mediated by the Na+/K+ pump.

A Vasilyev1, K Khater, R F Rakowski.   

Abstract

A ouabain sensitive inward current occurs in Xenopus oocytes in Na+ and K(+)-free solutions. Several laboratories have investigated the properties of this current and suggested that acidic extracellular pH (pHo) produces a conducting pathway through the Na+/K+ pump that is permeable to H+ and blocked by [Na+]o. An alternative suggestion is that the current is mediated by an electrogenic H(+)-ATPase. Here we investigate the effect of pHo and [Na+]o on both transient and steady-state ouabain-sensitive current. At alkaline or neutral pHo the relaxation rate of pre-steady-state current is an exponential function of voltage. Its U-shaped voltage dependence becomes apparent at acidic pHo, as predicted by a model in which protonation of the Na+/K+ pump reduces the energy barrier between the internal solution and the Na+ occluded state. The model also predicts that acidic pHo increases steady-state current leak through the pump. The apparent pK of the titratable group(s) is approximately 6, suggesting that histidine is involved in induction of the conductance pathway. 22Na efflux experiments in squid giant axon and current measurements in oocytes at acidic pHo suggest that both Na+ and H+ are permeant. The acid-induced inward current is reduced by high [Na+]o, consistent with block by Na+. A least squares analysis predicts that H+ is four orders of magnitude more permeant than Na+, and that block occurs when 3 Na+ ions occupy a low affinity binding site (K(0.5) = 130 +/- 30 m M) with a dielectric coefficient of 0.23 +/- 0.03. These data support the conclusion that the ouabain-sensitive conducting pathway is a result of passive leak of both Na+ and H+ through the Na+/K+ pump.

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Year:  2004        PMID: 15138746      PMCID: PMC1357233          DOI: 10.1007/s00232-004-0660-4

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  21 in total

1.  Voltage dependence of the apparent affinity for external Na(+) of the backward-running sodium pump.

Authors:  P De Weer; D C Gadsby; R F Rakowski
Journal:  J Gen Physiol       Date:  2001-04       Impact factor: 4.086

2.  ATP hydrolysis associated with an uncoupled sodium flux through the sodium pump: evidence for allosteric effects of intracellular ATP and extracellular sodium.

Authors:  I M Glynn; S J Karlish
Journal:  J Physiol       Date:  1976-04       Impact factor: 5.182

3.  Variable stoichiometry in reconstituted shark Na,K-ATPase engaged in uncoupled efflux.

Authors:  F Cornelius
Journal:  Biochim Biophys Acta       Date:  1990-07-24

4.  Uncoupled Na+-efflux on reconstituted shark Na,K-ATPase is electrogenic.

Authors:  F Cornelius
Journal:  Biochem Biophys Res Commun       Date:  1989-04-28       Impact factor: 3.575

5.  Protons as substitutes for sodium and potassium in the sodium pump reaction.

Authors:  C Polvani; R Blostein
Journal:  J Biol Chem       Date:  1988-11-15       Impact factor: 5.157

6.  Simultaneous measurement of changes in current and tracer flux in voltage-clamped squid giant axon.

Authors:  R F Rakowski
Journal:  Biophys J       Date:  1989-04       Impact factor: 4.033

7.  A negative slope in the current-voltage relationship of the Na+/K+ pump in Xenopus oocytes produced by reduction of external [K+].

Authors:  R F Rakowski; L A Vasilets; J LaTona; W Schwarz
Journal:  J Membr Biol       Date:  1991-04       Impact factor: 1.843

8.  Stoichiometry and voltage dependence of the sodium pump in voltage-clamped, internally dialyzed squid giant axon.

Authors:  R F Rakowski; D C Gadsby; P De Weer
Journal:  J Gen Physiol       Date:  1989-05       Impact factor: 4.086

9.  Steady-state current-voltage relationship of the Na/K pump in guinea pig ventricular myocytes.

Authors:  D C Gadsby; M Nakao
Journal:  J Gen Physiol       Date:  1989-09       Impact factor: 4.086

10.  Sodium extrusion by internally dialyzed squid axons.

Authors:  F J Brinley; L J Mullins
Journal:  J Gen Physiol       Date:  1967-11       Impact factor: 4.086

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  14 in total

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Authors:  Hanne Poulsen; Himanshu Khandelia; J Preben Morth; Maike Bublitz; Ole G Mouritsen; Jan Egebjerg; Poul Nissen
Journal:  Nature       Date:  2010-08-15       Impact factor: 49.962

2.  The third sodium binding site of Na,K-ATPase is functionally linked to acidic pH-activated inward current.

Authors:  Ciming Li; Käthi Geering; Jean-Daniel Horisberger
Journal:  J Membr Biol       Date:  2007-03-08       Impact factor: 1.843

3.  Sodium and proton effects on inward proton transport through Na/K pumps.

Authors:  Travis J Mitchell; Camila Zugarramurdi; J Fernando Olivera; Craig Gatto; Pablo Artigas
Journal:  Biophys J       Date:  2014-06-17       Impact factor: 4.033

4.  The role of the third extracellular loop of the Na+,K+-ATPase alpha subunit in a luminal gating mechanism.

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Journal:  J Physiol       Date:  2005-03-17       Impact factor: 5.182

5.  Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes.

Authors:  Susan Spiller; Thomas Friedrich
Journal:  World J Biol Chem       Date:  2014-05-26

6.  Selectivity of externally facing ion-binding sites in the Na/K pump to alkali metals and organic cations.

Authors:  Ian M Ratheal; Gail K Virgin; Haibo Yu; Benoît Roux; Craig Gatto; Pablo Artigas
Journal:  Proc Natl Acad Sci U S A       Date:  2010-10-11       Impact factor: 11.205

7.  The two C-terminal tyrosines stabilize occluded Na/K pump conformations containing Na or K ions.

Authors:  Natascia Vedovato; David C Gadsby
Journal:  J Gen Physiol       Date:  2010-06-14       Impact factor: 4.086

8.  Altered Na+ transport after an intracellular alpha-subunit deletion reveals strict external sequential release of Na+ from the Na/K pump.

Authors:  Siddhartha Yaragatupalli; J Fernando Olivera; Craig Gatto; Pablo Artigas
Journal:  Proc Natl Acad Sci U S A       Date:  2009-08-24       Impact factor: 11.205

9.  Hyperpolarization-activated inward leakage currents caused by deletion or mutation of carboxy-terminal tyrosines of the Na+/K+-ATPase {alpha} subunit.

Authors:  Susan Meier; Neslihan N Tavraz; Katharina L Dürr; Thomas Friedrich
Journal:  J Gen Physiol       Date:  2010-02       Impact factor: 4.086

10.  Somatic mutations in ATP1A1 and CACNA1D underlie a common subtype of adrenal hypertension.

Authors:  Elena A B Azizan; Hanne Poulsen; Petronel Tuluc; Junhua Zhou; Michael V Clausen; Andreas Lieb; Carmela Maniero; Sumedha Garg; Elena G Bochukova; Wanfeng Zhao; Lalarukh Haris Shaikh; Cheryl A Brighton; Ada E D Teo; Anthony P Davenport; Tanja Dekkers; Bas Tops; Benno Küsters; Jiri Ceral; Giles S H Yeo; Sudeshna Guha Neogi; Ian McFarlane; Nitzan Rosenfeld; Francesco Marass; James Hadfield; Wojciech Margas; Kanchan Chaggar; Miroslav Solar; Jaap Deinum; Annette C Dolphin; I Sadaf Farooqi; Joerg Striessnig; Poul Nissen; Morris J Brown
Journal:  Nat Genet       Date:  2013-08-04       Impact factor: 38.330

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