A pharmacodynamic and pharmacokinetic assessment of a new alpha‐ adrenoceptor antagonist, doxazosin (UK33274) in normotensive subjects.
- 1 May 1982
- journal article
- clinical trial
- Published by Wiley in British Journal of Clinical Pharmacology
- Vol. 13 (5), 699-703
- https://doi.org/10.1111/j.1365-2125.1982.tb01439.x
Abstract
1 Doxazosin is a quinazoline derivative, related to prazosin, recently developed for the treatment of hypertension. 2 The intravenous administration of doxazosin (12 micrograms/kg) to six healthy normotensive subjects resulted in significant fall in erect blood pressure, with a corresponding increase in heart rate, but there were no significant changes in supine blood pressure or heart rate. 3 The changes in blood pressure and heart rate were maximal at 6 h after intravenous dosing. With prazosin the maximum effects occurred within the first hours. 4 Pressor response studies with phenylephrine confirmed that doxazosin is a relatively selective postsynaptic alpha‐ adrenoceptor antagonist. 5 The mean elimination half‐life of doxazosin was 11 h. This compared with a T1/2 of 2.5 h for prazosin.Keywords
This publication has 6 references indexed in Scilit:
- Immediate cardiovascular responses to oral prazosin—Effects of concurrent β-blockersClinical Pharmacology & Therapeutics, 1981
- Determination of the vasodilator UK33274 by high-performance liquid chromatography using fluorescence detectionJournal of Chromatography B: Biomedical Sciences and Applications, 1980
- Prazosin and its analogues UK-18,596 and UK-33,274: a comparative study on cardiovascular effects and alpha-adrenoceptor blocking activities.1980
- Prazosin, a selective antagonist of post-synaptic alpha-adrenoceptors [proceedings].1977
- Prazosin: the first-dose phenomenon.BMJ, 1976