Correlation between plasma concentration of cilazapril and haemodynamic and hormonal effects in healthy man.


Autoria(s): Burnier M.; Mooser V.; Nussberger J.; Waeber B.; Brunner H.R.
Data(s)

1989

Resumo

1. The haemodynamic and humoral effects of cilazapril, a new angiotensin converting enzyme (ACE) inhibitor, were evaluated in normotensive healthy volunteers. 2. Single oral doses of 1.25, 2.5, 5 and 10 mg of cilazapril inhibited ACE by greater than or equal to 90% and induced the expected pattern of changes of the renin-angiotensin-aldosterone-system. 3. Cilazapril had a long duration of action, since some ACE inhibition was still present 72 h after drug intake. 4. Cilazapril administered intravenously at doses of 5 and 20 micrograms kg-1 for 24 h did not produce any significant effects. 5. During repeated administration of cilazapril for 8 days, no accumulation of cilazaprilat was observed and the clinical tolerance was excellent. 6. In normal volunteers, cilazapril administered orally acts as a potent inhibitor of converting enzyme.

Identificador

http://serval.unil.ch/?id=serval:BIB_42FE91162326

isbn:0306-5251

pmid:2527532

isiid:A1989AK52100009

Idioma(s)

en

Fonte

British journal of clinical pharmacology, vol. 27 Suppl 2, pp. 189S-197S

Palavras-Chave #Administration, Oral; Adult; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Cilazapril; Heart Rate; Hemodynamics; Hormones; Humans; Infusions, Intravenous; Male; Pyridazines; Time Factors
Tipo

info:eu-repo/semantics/article

article