Literature DB >> 7042738

Bromocriptine does not inhibit the aldosterone response to sodium depletion.

R M Carey, G R Van Loon.   

Abstract

This study was designed to investigate the influence of the dopamine agonist, bromocriptine, on the renin-angiotensin-aldosterone system during dietary sodium restriction. Five normal white male volunteer subjects were studied in metabolic balance at constant 150 meq sodium, 60 meq potassium intake, and then daily for 7 days on an isocaloric constant diet of 10 meq sodium and 60 meq potassium/day. The subjects were studied once during administration of bromocriptine and again in the presence of bromocriptine placebo. After a stepwise daily decrease in urinary sodium excretion, sodium balance was achieved on the sixth day of low sodium intake. Renal sodium conservation in response to dietary sodium restriction was associated with parallel increases in PRA, plasma aldosterone concentration, and urinary aldosterone excretion. These changes were not significantly different during placebo and bromocriptine administration. Bromocriptine was active at the pituitary dopamine receptor, as serum PRL concentrations were suppressed to undetectable levels. The results indicate that bromocriptine does not alter the response of the renin-angiotensin-aldosterone system to sodium restriction.

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Year:  1982        PMID: 7042738     DOI: 10.1210/jcem-55-1-162

Source DB:  PubMed          Journal:  J Clin Endocrinol Metab        ISSN: 0021-972X            Impact factor:   5.958


  2 in total

1.  Role of dopamine in the regulation of aldosterone and 18-hydroxycorticosterone secretion in man.

Authors:  J R Sowers; F W Beck
Journal:  J Endocrinol Invest       Date:  1984-10       Impact factor: 4.256

2.  Effects of the dopaminergic agonist cianergoline on blood pressure, the renin-angiotensin-aldosterone axis and the sympathetic nervous system in patients with essential hypertension.

Authors:  G Bise; C Foletti; C Beretta-Piccoli; P Weidmann; W H Ziegler; R Mordasini; C Bachmann
Journal:  Eur J Clin Pharmacol       Date:  1985       Impact factor: 2.953

  2 in total

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