Literature DB >> 3492606

Influence of external barium and potassium on potassium efflux in depolarized frog sartorius muscles.

B C Spalding, J G Swift, P Horowicz.   

Abstract

Efflux of 42K+ was measured in frog sartorius muscles equilibrated in depolarizing solutions with external K+ concentrations [( K+]0) between 75 and 300 mM and NaCl concentrations of 60, 120, or 240 mM. For several combinations of KCl and NaCl, steady-state internal potentials (Vi) were the same for different [K+]0. For the range of Vi examined, K+ efflux occurs principally through the K+ inward rectifier channels. When external K+ is removed Vi remains constant for 2 to 3 hr because of the high membrane conductance to Cl-, but K+ efflux drops by about one order of magnitude. External Ba2+ in the presence or absence of external K+ produces an inhibition of K+ efflux described by a relation of the form u = (u1/(1 + C [Ba2+]0] + u2, where u is the uninhibited fraction of K+ efflux; u1, u2 and C are constants; and u1 + u2 = 1. C depends both on [K+]0 and Vi. When [K+]0 greater than or equal to 75 mM, increasing [K+]0 at constant Vi reduces Ba2+ sensitivity. For constant Vi greater than or equal to -30 mV, Ba2+ sensitivity is less when [K+]0 = 0 than when [K+]0 greater than or equal to 75 mM. When [K+]0 = 0, Ba2+ sensitivity decreases as Vi is made more positive. The dependence of the Ba2+ sensitivity on Vi at constant [K+]0 is greater when [K+]0 = 0 than when [K+]0 greater than or equal to 75 mM. Both the activation of K+ efflux by external K+ and the Ba2+ inhibition of K+ efflux can be explained on the basis of two membrane control sites associated with each channel. When both sites are occupied by K+, the channels are in a high flux state. When one or both sites are empty, the channels are in a low, nonzero flux state. When Ba2+ occupies either site, K+ efflux is further reduced. The reduction of Ba2+-sensitivity by increasing [K+]0 at high [K+]0 is attributable to the displacement of Ba2+ from the control sites by K+. The increased Ba2+ sensitivity produced by going from [K+]0 = 0 to [K+] greater than or equal to 75 mM when Vi greater than or equal to -30 mV is attributable to states in which Ba2+ occupies one site and K+ the other when [K+]0 not equal to 0.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 3492606     DOI: 10.1007/BF01870806

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


  22 in total

1.  POTASSIUM CONTRACTURES AND CREATINE PHOSPHATE BREAKDOWN IN FROG MUSCLE.

Authors:  C EDWARDS; F D CARLSON
Journal:  Biochim Biophys Acta       Date:  1964-07-29

2.  Movement of inorganic ions across the membrane of striated muscle.

Authors:  R H ADRIAN
Journal:  Circulation       Date:  1962-11       Impact factor: 29.690

3.  THE RUBIDIUM AND POTASSIUM PERMEABILITY OF FROG MUSCLE MEMBRANE.

Authors:  R H ADRIAN
Journal:  J Physiol       Date:  1964-12       Impact factor: 5.182

4.  The influence of potassium and chloride ions on the membrane potential of single muscle fibres.

Authors:  A L HODGKIN; P HOROWICZ
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

5.  Voltage-dependent ATP-sensitive potassium channels of skeletal muscle membrane.

Authors:  A E Spruce; N B Standen; P R Stanfield
Journal:  Nature       Date:  1985 Aug 22-28       Impact factor: 49.962

6.  Inward rectification in frog skeletal muscle fibres and its dependence on membrane potential and external potassium.

Authors:  C A Leech; P R Stanfield
Journal:  J Physiol       Date:  1981       Impact factor: 5.182

7.  Potassium channels as multi-ion single-file pores.

Authors:  B Hille; W Schwarz
Journal:  J Gen Physiol       Date:  1978-10       Impact factor: 4.086

8.  The dual effect of rubidium ions on potassium efflux in depolarized frog skeletal muscle.

Authors:  B C Spalding; J G Swift; O Senyk; P Horowicz
Journal:  J Membr Biol       Date:  1982       Impact factor: 1.843

9.  The role of the electrochemical gradient in determining potassium fluxes in frog striated muscle.

Authors:  P Horowicz; P W Gage; R S Eisenberg
Journal:  J Gen Physiol       Date:  1968-05-01       Impact factor: 4.086

10.  Blocking effects of barium and hydrogen ions on the potassium current during anomalous rectification in the starfish egg.

Authors:  S Hagiwara; S Miyazaki; W Moody; J Patlak
Journal:  J Physiol       Date:  1978-06       Impact factor: 5.182

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  4 in total

1.  Response of chloride efflux from skeletal muscle of Rana pipiens to changes of temperature and membrane potential and diethylpyrocarbonate treatment.

Authors:  B C Spalding; P Taber; J G Swift; P Horowicz
Journal:  J Membr Biol       Date:  1991-09       Impact factor: 1.843

2.  Zinc inhibition of chloride efflux from skeletal muscle of Rana pipiens and its modification by external pH and chloride activity.

Authors:  B C Spalding; P Taber; J G Swift; P Horowicz
Journal:  J Membr Biol       Date:  1990-07       Impact factor: 1.843

3.  Zinc inhibition of potassium efflux in depolarized frog muscle and its modification by external hydrogen ions and diethylpyrocarbonate treatment.

Authors:  B C Spalding; J G Swift; P Horowicz
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

4.  In skeletal muscle the relaxation of the resting membrane potential induced by K(+) permeability changes depends on Cl(-) transport.

Authors:  R J Geukes Foppen
Journal:  Pflugers Arch       Date:  2003-11-27       Impact factor: 3.657

  4 in total

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