Literature DB >> 8941920

AVP and aldosterone at physiological concentrations have synergistic effects on Na+ transport in rat CCD.

C T Hawk1, L Li, J A Schafer.   

Abstract

These studies examined whether the previously reported synergism between pharmacological doses of deoxycorticosterone (DOC) and arginine vasopressin (AVP) also occur at physiological concentrations of aldosterone and AVP. We examined the dose-response of salt transport, as measured by the lumen-to-bath 22Na+ flux (J1 --> b) and transepithelial voltage (VT), and of osmotic water permeability (Pf), to AVP in isolated perfused cortical collecting ducts (CCDs) from three groups of rats: (1) implanted with a 1 mg d-aldosterone pellet, which produced a moderately elevated, but physiologically relevant, plasma aldosterone concentration of 18.4 +/- 2.6 ng/dl; (2) implanted with a 2.5 mg DOC pellet (a high pharmacological dose); and (3) untreated rats, Pf reached the same maximal value in all three groups, and the concentration of AVP producing one-half the maximal Pf response (K0.5) was not significantly different among the three groups, ranging from 5 to 10 pM. There was a significantly greater increase in J1 --> b and hyperpolarization of VT with increasing AVP in both groups of treated rats than in the untreated group. The maximum values of J1 --> b and VT achieved at high AVP concentrations were not significantly different in CCDs from the aldosterone-treated and DOC-treated groups, but they were significantly higher than in the CCDs from untreated rats. Although maximal VT values achieved with DOC and aldosterone treatment were the same, the AVP K0.5 for VT were significantly lower in the DOC-treated than in the aldosterone-treated group. Although not statistically significant, the same trend was observed for J1 --> b. We conclude that AVP and aldosterone synergistically stimulate Na+ reabsorption at physiological concentrations of both hormones; however, VT (and probably Na+ reabsorption, which is generally proportional to VT) reaches maximum values at lower AVP concentrations when pharmacological doses of DOC are employed.

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Year:  1996        PMID: 8941920

Source DB:  PubMed          Journal:  Kidney Int Suppl        ISSN: 0098-6577            Impact factor:   10.545


  12 in total

1.  Activation of ENaC by AVP contributes to the urinary concentrating mechanism and dilution of plasma.

Authors:  Elena Mironova; Yu Chen; Alan C Pao; Karl P Roos; Donald E Kohan; Vladislav Bugaj; James D Stockand
Journal:  Am J Physiol Renal Physiol       Date:  2014-11-12

2.  Dominant factors that govern pressure natriuresis in diuresis and antidiuresis: a mathematical model.

Authors:  Robert Moss; Anita T Layton
Journal:  Am J Physiol Renal Physiol       Date:  2014-02-19

Review 3.  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

4.  Transcriptome of a mouse kidney cortical collecting duct cell line: effects of aldosterone and vasopressin.

Authors:  M Robert-Nicoud; M Flahaut; J M Elalouf; M Nicod; M Salinas; M Bens; A Doucet; P Wincker; F Artiguenave; J D Horisberger; A Vandewalle; B C Rossier; D Firsov
Journal:  Proc Natl Acad Sci U S A       Date:  2001-02-20       Impact factor: 11.205

5.  Role of vasopressin in rat distal colon function.

Authors:  Esther Cristià; Concepció Amat; Richard J Naftalin; Miquel Moretó
Journal:  J Physiol       Date:  2006-11-02       Impact factor: 5.182

6.  Activation of the epithelial Na+ channel in the collecting duct by vasopressin contributes to water reabsorption.

Authors:  Vladislav Bugaj; Oleh Pochynyuk; James D Stockand
Journal:  Am J Physiol Renal Physiol       Date:  2009-08-19

7.  Vasopressin potentiates mineralocorticoid selectivity by stimulating 11 beta hydroxysteroid deshydrogenase in rat collecting duct.

Authors:  N Alfaidy; M Blot-Chabaud; J P Bonvalet; N Farman
Journal:  J Clin Invest       Date:  1997-11-15       Impact factor: 14.808

Review 8.  Lithium: a versatile tool for understanding renal physiology.

Authors:  Bellamkonda K Kishore; Carolyn M Ecelbarger
Journal:  Am J Physiol Renal Physiol       Date:  2013-02-13

9.  The role of the epithelial Na(+) channel (ENaC) in high AVP but low aldosterone states.

Authors:  James D Stockand
Journal:  Front Physiol       Date:  2012-07-31       Impact factor: 4.566

10.  Recording ion channels in isolated, split-opened tubules.

Authors:  Elena Mironova; Vladislav Bugay; Oleh Pochynyuk; Alexander Staruschenko; James D Stockand
Journal:  Methods Mol Biol       Date:  2013
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