Literature DB >> 1234508

Bioassay of aldosterone antagonists in normal human subjects: a relationship between the level of plasma uric acid before treatment and apparent drug responses.

L E Ramsay, P Hessian, M J Tidd.   

Abstract

The activity of single doses of SC-23992, a new aldosterone antagonist, and spironolactone in reversing the effects of fludrocortisone on urinary electrolyte composition in normal subjects was compared with that of placebo in a double-blind crossover study. 2 SC-23992 (50 mg) and spironolactone (125 mg) each significantly increased sodium excretion and the sodium : potassium (Na/K) ratio, and decreased potassium excretion, when compared with placebo. The response to the two active drugs did not differ significantly. 3 The urine Na/K ratio, and log10 Na/K, in response to spironolactone correlated negatively with the level of plasma uric acid measured 12 h before treatment. Similar trends were present after SC-23992 and placebo treatments. 4 It is suggested that the correlations between plasma uric acid and apparent drug response reflect a correlation between plasma uric acid and the aldosterone secretion rate in normal subjects. The sensitivity of this method of bioassay may be improved by suppressing endogenous aldosterone prior to medication.

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Year:  1975        PMID: 1234508      PMCID: PMC1402582          DOI: 10.1111/j.1365-2125.1975.tb01587.x

Source DB:  PubMed          Journal:  Br J Clin Pharmacol        ISSN: 0306-5251            Impact factor:   4.335


  16 in total

1.  [TUBULAR EFFECTS AND RENAL ELIMINATION OF SPIROLACTONES].

Authors:  G HOLLMANN; G SENFT; C WERNER
Journal:  Naunyn Schmiedebergs Arch Exp Pathol Pharmakol       Date:  1964-06-11

2.  Human assay of electrolyte-active steroids and their antagonists.

Authors:  E J ROSS
Journal:  Clin Sci       Date:  1962-10       Impact factor: 6.124

3.  Studies on the renal excretion of salicylate in the dog.

Authors:  I M WEINER; J A WASHINGTON; G H MUDGE
Journal:  Bull Johns Hopkins Hosp       Date:  1959-11

4.  Blocking the renal electrolyte effects of mineralocorticoids with an orally active steroidal spirolactone.

Authors:  C M KAGAWA
Journal:  Endocrinology       Date:  1960-07       Impact factor: 4.736

5.  Infusion of aldosterone, 9-alpha-fluorohydrocortisone and antidiuretic hormone into the renal artery of normal and adrenalectomized, unanesthetized dogs: effect on electrolyte and water excretion.

Authors:  A C BARGER; R D BERLIN; J F TULENKO
Journal:  Endocrinology       Date:  1958-06       Impact factor: 4.736

6.  The mode of action and clinical use of spirolactones.

Authors:  A Manitius; T Suchecki
Journal:  Mater Med Pol       Date:  1972 Apr-Jun

7.  On the clinical evaluation of diuretics with particular reference to a new phthalimidine diuretic, clorexolone.

Authors:  A F Lant; W I Baba; G M Wilson
Journal:  Clin Pharmacol Ther       Date:  1966 Mar-Apr       Impact factor: 6.875

8.  Urate excretion.

Authors:  M D Milne
Journal:  Proc R Soc Med       Date:  1966-04

9.  Bioassay of adrenal cortical steroids on the basis of electrolyte excretion by rats: effects of 11-desoxy and 11-oxy-steroids.

Authors:  B B JOHNSON
Journal:  Endocrinology       Date:  1954-02       Impact factor: 4.736

10.  Stimulation and suppression of aldosterone in plasma of normal man and in primary aldosteronism.

Authors:  R Horton
Journal:  J Clin Invest       Date:  1969-07       Impact factor: 14.808

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  10 in total

1.  A relationship between plasma uric acid concentration and the apparent response to frusemide in normal subjects.

Authors:  L E Ramsay; M J Tidd; R M Auty; D Levine; R A Branch
Journal:  Br J Clin Pharmacol       Date:  1975-08       Impact factor: 4.335

2.  Plasma uric acid and spironolactone response in healthy subjects.

Authors:  L E Ramsay; J R Shelton; I R Harrison
Journal:  Br J Clin Pharmacol       Date:  1977-04       Impact factor: 4.335

3.  Canrenone--the principal active metabolite of spironolactone?

Authors:  L E Ramsay; J R Shelton; D Wilkinson; M J Tidd
Journal:  Br J Clin Pharmacol       Date:  1976-08       Impact factor: 4.335

4.  Comparison of prorenoate potassium and spironolactone after repeated doses and steady state plasma levels of active metabolites.

Authors:  G T McInnes; J R Shelton; I R Harrison; R M Perkins; R F Palmer
Journal:  Br J Clin Pharmacol       Date:  1982-02       Impact factor: 4.335

5.  The influence of sodium and potassium supplements on the diuretic responses to frusemide administration in normal subjects.

Authors:  R A Branch; E Cole; C E Horth; L Jackson; L E Ramsay; J Shelton
Journal:  Br J Pharmacol       Date:  1978-10       Impact factor: 8.739

6.  Quantitative comparison of aldosterone antagonists in normal human subjects: prediction of therapeutic potency.

Authors:  G T McInnes; I R Harrison; J R Shelton; R M Perkins
Journal:  Br J Clin Pharmacol       Date:  1981-11       Impact factor: 4.335

7.  Assessment of the antimineralocorticoid effect of RU 28318 in healthy men with induced exogenous and endogenous hypermineralocorticism.

Authors:  A Ulmann; C Bertagna; A Le Go; J M Husson; A Tache; P Sassano; J Menard; P Corvol
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

8.  Relative potency and structure activity relationships of aldosterone antagonists in healthy man: correlation with animal experience.

Authors:  G T McInnes; J R Shelton; L E Ramsay; I R Harrison; M J Asbury; J M Clarke; R M Perkins; G R Venning
Journal:  Br J Clin Pharmacol       Date:  1982-03       Impact factor: 4.335

9.  The pharmacodynamics of single doses of prorenoate potasssium and spironolactone in fludrocortisone treated normal subjects.

Authors:  L E Ramsay; J R Shelton; M J Tidd
Journal:  Br J Clin Pharmacol       Date:  1976-06       Impact factor: 4.335

10.  Antagonism of endogenous mineralocorticoids in normal subjects by prorenoate potassium and spironolactone.

Authors:  D Levine; L Ramsay; R Auty; R Branch; M Tidd
Journal:  Eur J Clin Pharmacol       Date:  1976-03-22       Impact factor: 2.953

  10 in total

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