The haemodynamic effects and pharmacokinetics of intravenous nicorandil in healthy volunteers |
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Authors: | D. L. Wolf J. J. Ferry A. E. Hearron M. O. Froeschke J. R. Luderer |
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Affiliation: | (1) Departments of Clinical Research, The Upjohn Research Clinics, The Upjohn Company, Kalamazoo, Michigan, USA;(2) Department of Clinical Pharmacokinetics, The Upjohn Research Clinics, The Upjohn Company, Kalamazoo, Michigan, USA;(3) Department of Biostatistics, The Upjohn Research Clinics, The Upjohn Company, Kalamazoo, Michigan, USA;(4) Clinical Pharmacology and Efficacy 7214-258-2, Upjohn Laboratories, The Upjohn Company, 49001 Kalamazoo, Michigan, USA |
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Abstract: | Summary We have studied the effects of intravenous nicorandil, a mixed arterial and venous vasodilator, in 48 healthy volunteers. Nicorandil (20, 28, 39, 54, 74, 103, 144, or 200 g·kg–1) or placebo were given over 5 min to subjects supine (16 subjects, 2 doses) or sitting (32 subjects, 1 dose) in a single-blind crossover design. Electro-cardiographic intervals, blood pressure, and heart rate were measured before and for 8 h after dosing. Blood and urine safety laboratory studies were also performed before and after dosing.All intravenous infusions of nicorandil and placebo were well tolerated and there were no clinically important safety concerns. The most frequent adverse event after nicorandil was headache (24 events by 19 subjects), although its occurrence was not strictly dose related. One subject experienced transient symptomatic hypotension (144 g·kg–1).Mean plasma nicorandil concentrations were dose-related and fell with a half-life of 0.7 to 1.2 h. Systemic clearance and volume of distribution tended to decrease as dose increased. Sitting subjects showed marginally lower (<20%) systemic clearances and larger values of Cmax and AUC.Nicorandil produced dose-related reductions in blood pressure, with consistent statistically significant differences from placebo after the 144 and 200 g·kg–1 doses. The falls in blood pressure were greater for diastolic pressure and in this supine position. At 200 g·kg–1, the mean falls in systolic/diastolic pressures (mm Hg) during the first hour were 10.9/14.7 supine and 6.1/9.1 sitting; systolic pressure returned to baseline after 8 h and diastolic pressure after 4 h. Heart rate increased transiently (mean peak increase of 17–24 bpm at the end of the 144 and 200 g·kg–1 infusions). Blood pressure and heart rate changes over time were statistically significantly correlated with plasma nicorandil concentrations. Individual areas under the blood pressure and heart rate change curves likewise correlated with plasma concentration curve areas. |
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Keywords: | Nicorandil vasodilator tolerance study blood pressure pharmacokinetics healthy volunteers |
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