Amitriptyline and ethanol: pharmacokinetic and pharmacodynamic interaction

Amitriptyline has clinically important interactions with ethanol. Five healthy volunteers received 25 mg of amitriptyline orally, preceded by one hour and followed for eight hours by oral ethanol (or juice), dosed to achieve and maintain blood ethanol concentrations of 800 mg/l. In the presence of e...

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Bibliographic Details
Published in:European journal of clinical pharmacology 1983-01, Vol.25 (3), p.325-331
Main Authors: DORIAN, P, SELLERS, E. M, REED, K. L, WARSH, J. J, HAMILTON, C, KAPLAN, H. L, FAN, T
Format: Article
Language:English
Subjects:
Adult
Amitriptyline - metabolism
Amitriptyline - pharmacology
Biological and medical sciences
Drug Interactions
Ethanol - pharmacology
Female
Humans
Kinetics
Male
Medical sciences
Mental Recall - drug effects
Neuropharmacology
Pharmacology. Drug treatments
Posture
Psychoanaleptics: cns stimulant, antidepressant agent, nootropic agent, mood stabilizer..., (alzheimer disease)
Psychology. Psychoanalysis. Psychiatry
Psychopharmacology
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Summary:Amitriptyline has clinically important interactions with ethanol. Five healthy volunteers received 25 mg of amitriptyline orally, preceded by one hour and followed for eight hours by oral ethanol (or juice), dosed to achieve and maintain blood ethanol concentrations of 800 mg/l. In the presence of ethanol, amitriptyline free plasma concentrations were increased by a logarithmic mean of 204%, 186% and 127% at 1.5, 2, and 2.5 h, respectively, and amitriptyline free AUC0-8h was increased by 48% +/- 13% (means +/- SEM) (t = 5.21, p less than 0.01). Nortriptyline total AUC0-8h was increased by 26.6% +/- 12% (means +/- SEM) (t = 2.21, p less than 0.09). At the time of peak amitriptyline plasma concentrations, mean postural sway was increased over baseline by 92% with, and 2% without ethanol; likewise, mean short term memory (word recall) was decreased over baseline by 71% with, and 37% without ethanol. Ethanol increases free amitriptyline plasma concentrations most dramatically during the period of drug absorption; this is due to a decrease in amitriptyline hepatic clearance, resulting in decreased first-pass extraction. Together with the pharmacodynamic interaction, the kinetic changes provide a rationale for the toxicity of this combination and its deleterious effects on psychomotor skills.
ISSN:0031-6970
1432-1041
DOI:10.1007/BF01037943