Literature DB >> 4054204

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

G Bise, C Foletti, C Beretta-Piccoli, P Weidmann, W H Ziegler, R Mordasini, C Bachmann.   

Abstract

Cianergoline is a new dopaminergic agonist with a predominant cardiovascular action. Its effects on blood pressure, the renin-angiotensin-aldosterone axis, the sympathetic nervous system and lipid metabolism were assessed in 20 patients with benign essential hypertension. Cianergoline given in increasing doses for 4 weeks (maximum daily dose 12 +/- 2 mg (SD)) and placebo both caused a slight decrease in arterial pressure, (from 159/104 to 152/98 mm Hg and from 154/104 to 149/103 mm, respectively; difference not significant). Supine and upright plasma renin activity, plasma aldosterone, norepinephrine, epinephrine and dopamine levels, urinary catecholamine excretion rates as well as serum prolactin, low and high density cholesterol and triglyceride concentrations were not changed after cianergoline or placebo. Total serum cholesterol and triglyceride levels decreased significantly after placebo, but were unchanged after cianergoline. 3 out of 10 patients in the cianergoline group complained of nausea. The findings indicate that the new dopaminergic agonist cianergoline exerts only a mild blood pressure lowering effect in patients with essential hypertension and does not modify the release of prolactin, lipid metabolism or the basal activity or postural responsiveness of the renin-angiotensin-aldosterone axis and of the sympathetic nervous system.

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Year:  1985        PMID: 4054204     DOI: 10.1007/BF00547364

Source DB:  PubMed          Journal:  Eur J Clin Pharmacol        ISSN: 0031-6970            Impact factor:   2.953


  36 in total

1.  Age versus urinary sodium for judging renin, aldosterone, and catecholamine levels: studies in normal subjects and patients with essential hypertension.

Authors:  P Weidmann; C Beretta-Piccoli; W H Ziegler; G Keusch; Z Glück; F C Reubi
Journal:  Kidney Int       Date:  1978-12       Impact factor: 10.612

2.  Inhibition of the plasma-aldosterone response to frusemide by bromocriptine.

Authors:  C R Edwards; P A Miall; J P Hanker; M O Thorner; E A Al-Dujaili; G M Besser
Journal:  Lancet       Date:  1975-11-08       Impact factor: 79.321

Review 3.  Pharmacology of bromocriptine in health and disease.

Authors:  A E Mehta; G Tolis
Journal:  Drugs       Date:  1979-05       Impact factor: 9.546

4.  Bromocriptine-induced modulation of plasma aldosterone response to acute stimulations.

Authors:  M Birkhäuser; A Riondel; M B Vallotton
Journal:  Acta Endocrinol (Copenh)       Date:  1979-06

5.  The effects of two analogs of dopamine on ganglionic transmission in the sympathetic nervous system.

Authors:  J M Kitzen; M R Strait; J P Long; W C De Groat
Journal:  J Pharmacol Exp Ther       Date:  1979-12       Impact factor: 4.030

6.  Bromocriptine does not inhibit the aldosterone response to sodium depletion.

Authors:  R M Carey; G R Van Loon
Journal:  J Clin Endocrinol Metab       Date:  1982-07       Impact factor: 5.958

7.  Bromocriptine: lack of effect on the angiotensin II and aldosterone responses to sodium deprivation.

Authors:  P F Semple; P A Mason
Journal:  Clin Endocrinol (Oxf)       Date:  1978-08       Impact factor: 3.478

8.  Dopaminergic modulation of pressor and hormonal responses in essential hypertension.

Authors:  J R Sowers; M S Golub; M E Berger; L A Whitfield
Journal:  Hypertension       Date:  1982 May-Jun       Impact factor: 10.190

9.  The effects of bromocriptine in patients with congestive heart failure.

Authors:  G S Francis; R Parks; J N Cohn
Journal:  Am Heart J       Date:  1983-07       Impact factor: 4.749

10.  Antihypertensive action of bromocriptine in neurogenic hypertensive dogs.

Authors:  J L Montastruc; P Montastruc
Journal:  Arch Int Pharmacodyn Ther       Date:  1981-08
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