Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol

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Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol. / Bendtsen, F; Henriksen, Jens Henrik Sahl.

In: Journal of Human Hypertension, Vol. 3 Suppl 1, 1989, p. 139-45.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Bendtsen, F & Henriksen, JHS 1989, 'Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol', Journal of Human Hypertension, vol. 3 Suppl 1, pp. 139-45.

APA

Bendtsen, F., & Henriksen, J. H. S. (1989). Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol. Journal of Human Hypertension, 3 Suppl 1, 139-45.

Vancouver

Bendtsen F, Henriksen JHS. Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol. Journal of Human Hypertension. 1989;3 Suppl 1:139-45.

Author

Bendtsen, F ; Henriksen, Jens Henrik Sahl. / Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol. In: Journal of Human Hypertension. 1989 ; Vol. 3 Suppl 1. pp. 139-45.

Bibtex

@article{6c8ec7e0328511df8ed1000ea68e967b,
title = "Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol",
abstract = "In an open, crossover study, the pharmacokinetic and pharmacodynamic profiles of lisinopril and enalapril, administered alone and in combination with propranolol, were evaluated in 12 volunteers. The maximum serum concentration (Cmax) of lisinopril and time to reach maximum concentration (Tmax) were 64 +/- 16 ng/ml and 7.5 +/- 1.5 h, respectively. The area under the serum curve (AUC) was 916 +/- 239 h. ng/ml. The Cmax of enalaprilat (89 +/- 34 ng/ml) was greater than that of lisinopril whilst Tmax was shorter (4.3 +/- 1.7 h) and AUC smaller (718 +/- 17 h.ng/ml) (P less than 0.01). Renal clearance of drug 48 h post-dosing showed that enalaprilat (164 +/- 38 ml/min) was cleared from plasma significantly more rapidly than lisinopril (82 +/- 16 ml/min) (P less than 0.001). Mean supine blood pressure decreased significantly with all treatments, as did heart rate. No significant changes were observed in either the serum concentrations or the urinary outputs of these ACE inhibitors following combination with propranolol, apart from a greater variability of Cmax after addition of propranolol to enalapril compared with lisinopril in combination.",
author = "F Bendtsen and Henriksen, {Jens Henrik Sahl}",
note = "Keywords: Adult; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Drug Interactions; Drug Therapy, Combination; Enalapril; Female; Heart Rate; Humans; Lisinopril; Male; Propranolol",
year = "1989",
language = "English",
volume = "3 Suppl 1",
pages = "139--45",
journal = "Journal of Human Hypertension",
issn = "0950-9240",
publisher = "nature publishing group",

}

RIS

TY - JOUR

T1 - Comparative pharmacokinetics and pharmacodynamics of lisinopril and enalapril, alone and in combination with propranolol

AU - Bendtsen, F

AU - Henriksen, Jens Henrik Sahl

N1 - Keywords: Adult; Angiotensin-Converting Enzyme Inhibitors; Blood Pressure; Drug Interactions; Drug Therapy, Combination; Enalapril; Female; Heart Rate; Humans; Lisinopril; Male; Propranolol

PY - 1989

Y1 - 1989

N2 - In an open, crossover study, the pharmacokinetic and pharmacodynamic profiles of lisinopril and enalapril, administered alone and in combination with propranolol, were evaluated in 12 volunteers. The maximum serum concentration (Cmax) of lisinopril and time to reach maximum concentration (Tmax) were 64 +/- 16 ng/ml and 7.5 +/- 1.5 h, respectively. The area under the serum curve (AUC) was 916 +/- 239 h. ng/ml. The Cmax of enalaprilat (89 +/- 34 ng/ml) was greater than that of lisinopril whilst Tmax was shorter (4.3 +/- 1.7 h) and AUC smaller (718 +/- 17 h.ng/ml) (P less than 0.01). Renal clearance of drug 48 h post-dosing showed that enalaprilat (164 +/- 38 ml/min) was cleared from plasma significantly more rapidly than lisinopril (82 +/- 16 ml/min) (P less than 0.001). Mean supine blood pressure decreased significantly with all treatments, as did heart rate. No significant changes were observed in either the serum concentrations or the urinary outputs of these ACE inhibitors following combination with propranolol, apart from a greater variability of Cmax after addition of propranolol to enalapril compared with lisinopril in combination.

AB - In an open, crossover study, the pharmacokinetic and pharmacodynamic profiles of lisinopril and enalapril, administered alone and in combination with propranolol, were evaluated in 12 volunteers. The maximum serum concentration (Cmax) of lisinopril and time to reach maximum concentration (Tmax) were 64 +/- 16 ng/ml and 7.5 +/- 1.5 h, respectively. The area under the serum curve (AUC) was 916 +/- 239 h. ng/ml. The Cmax of enalaprilat (89 +/- 34 ng/ml) was greater than that of lisinopril whilst Tmax was shorter (4.3 +/- 1.7 h) and AUC smaller (718 +/- 17 h.ng/ml) (P less than 0.01). Renal clearance of drug 48 h post-dosing showed that enalaprilat (164 +/- 38 ml/min) was cleared from plasma significantly more rapidly than lisinopril (82 +/- 16 ml/min) (P less than 0.001). Mean supine blood pressure decreased significantly with all treatments, as did heart rate. No significant changes were observed in either the serum concentrations or the urinary outputs of these ACE inhibitors following combination with propranolol, apart from a greater variability of Cmax after addition of propranolol to enalapril compared with lisinopril in combination.

M3 - Journal article

C2 - 2550636

VL - 3 Suppl 1

SP - 139

EP - 145

JO - Journal of Human Hypertension

JF - Journal of Human Hypertension

SN - 0950-9240

ER -

ID: 18692649