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Influence of acetylator status on the haemodynamic effects and pharmacokinetics of cadralazine in healthy subjects.
Author(s) -
Brunel P,
Lecaillon JB,
Guyene TT,
Imhof P,
Menard J
Publication year - 1990
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/j.1365-2125.1990.tb03672.x
Subject(s) - metabolite , pharmacokinetics , pharmacology , plasma renin activity , cmax , active metabolite , hemodynamics , plasma concentration , oral administration , chemistry , vasodilation , drug , blood pressure , renin–angiotensin system , medicine
1. Cadralazine is a new antihypertensive agent which causes peripheral vasodilation, probably mediated by a hydrazinopyridazine metabolite. 2. The possible influence of acetylator status on the pharmacokinetics and haemodynamics of the drug was studied in six fast and six slow acetylators over a period of 24 h after administration of a single 10 mg oral dose. 3. There were no differences between the two groups in AUC and Cmax values of cadralazine and apparent metabolite, the latter defined as the sum of the free and conjugated hydrazinopyridazine. Peak plasma concentrations of these compounds were reached after 1 h. Thereafter, the concentration of the metabolite declined more slowly than that of cadralazine. 4. No effects on blood pressure were noted. Changes in heart rate and plasma renin were delayed by 3‐5 h with respect to the time‐course of drug and metabolite in plasma; maximum responses occurred at 4‐6 h after drug administration. The extent of the increase in plasma renin activity was slightly greater in slow than in fast acetylators, but the difference was not significant statistically.