Literature DB >> 2164011

Cell sodium-induced recruitment of Na(+)-K(+)-ATPase pumps in rabbit cortical collecting tubules is aldosterone-dependent.

M Blot-Chabaud1, F Wanstok, J P Bonvalet, N Farman.   

Abstract

The influence of intracellular sodium concentration ( [Na+]i) on the number of Na(+)-K(+)-ATPase pumps was examined in cortical collecting tubules (CCD) of kidneys from rabbits in different aldosterone conditions. Specific [3H]ouabain binding was measured in isolated CCD with various [Na+]i. Experiments were performed on adrenalectomized rabbits receiving only a substitutive dose of dexamethasone and on adrenalectomized rabbits replete with aldosterone. In aldosterone-replete rabbits, the number of binding sites increased linearly with [Na+]i, from 16 fmol/nl tubular volume at 15 mM Na+i to 39 fmol/nl tubular volume at 140 mM Na+i. Neither actinomycin D (5 microM) nor cycloheximide (10 microM) prevented this [Na+]i-dependent increase. In adrenalectomized rabbits, the number of ouabain-binding sites was reduced and did not increase with [Na+]i. These results are in favor of the presence of a "latent" pool of pumps in CCD, rapidly recruited under [Na+]i influence. Aldosterone appears to be required for the constitution and/or activation of this pool.

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Year:  1990        PMID: 2164011

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

1.  Regulation of Na+,K+-ATPase by persistent sodium accumulation in adult rat thalamic neurones.

Authors:  V V Senatorov; P K Stys; B Hu
Journal:  J Physiol       Date:  2000-06-01       Impact factor: 5.182

2.  Intracellular Na+ controls cell surface expression of Na,K-ATPase via a cAMP-independent PKA pathway in mammalian kidney collecting duct cells.

Authors:  Manlio Vinciguerra; Georges Deschênes; Udo Hasler; David Mordasini; Martine Rousselot; Alain Doucet; Alain Vandewalle; Pierre-Yves Martin; Eric Féraille
Journal:  Mol Biol Cell       Date:  2003-04-04       Impact factor: 4.138

3.  Sodium transport is modulated by p38 kinase-dependent cross-talk between ENaC and Na,K-ATPase in collecting duct principal cells.

Authors:  Yu-Bao Wang; Valérie Leroy; Arvid B Maunsbach; Alain Doucet; Udo Hasler; Eva Dizin; Thomas Ernandez; Sophie de Seigneux; Pierre-Yves Martin; Eric Féraille
Journal:  J Am Soc Nephrol       Date:  2013-10-31       Impact factor: 10.121

4.  Transepithelial glucose transport and Na+/K+ homeostasis in enterocytes: an integrative model.

Authors:  Kristian Thorsen; Tormod Drengstig; Peter Ruoff
Journal:  Am J Physiol Cell Physiol       Date:  2014-06-04       Impact factor: 4.249

Review 5.  Coordinated Control of ENaC and Na+,K+-ATPase in Renal Collecting Duct.

Authors:  Eric Feraille; Eva Dizin
Journal:  J Am Soc Nephrol       Date:  2016-05-17       Impact factor: 10.121

6.  Potassium excretion during antinatriuresis: perspective from a distal nephron model.

Authors:  Alan M Weinstein
Journal:  Am J Physiol Renal Physiol       Date:  2011-11-23

Review 7.  Regulation of Na+,K(+)-ATPase gene expression: a model to study terminal differentiation.

Authors:  G Celsi; Z M Wang
Journal:  Pediatr Nephrol       Date:  1993-10       Impact factor: 3.714

8.  Role of enhanced Na+ entry in the control of Na,K-ATPase gene expression by serum.

Authors:  A Kirtane; N Ismail-Beigi; F Ismail-Beigi
Journal:  J Membr Biol       Date:  1994-01       Impact factor: 1.843

Review 9.  Aldosterone receptor antagonists: biology and novel therapeutical applications.

Authors:  P Magni; M Motta
Journal:  J Endocrinol Invest       Date:  2003-08       Impact factor: 4.256

10.  Mineralocorticoid modulation of apical and basolateral membrane H+/OH-/HCO3- transport processes in the rabbit inner stripe of outer medullary collecting duct.

Authors:  S R Hays
Journal:  J Clin Invest       Date:  1992-07       Impact factor: 14.808

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