Evaluation and comparison of the interaction between alcohol and moclobemide or clomipramine in healthy subjects
- PMID: 2296627
- DOI: 10.1007/BF02245787
Evaluation and comparison of the interaction between alcohol and moclobemide or clomipramine in healthy subjects
Abstract
The interaction of clomipramine and moclobemide with alcohol was compared in a double blind parallel groups study in 24 healthy volunteers. Moclobemide was given at the highest recommended therapeutic dose (200 mg t.i.d.) and clomipramine in a subtherapeutic dose (25 mg b.i.d.) because of its poor tolerance in healthy subjects. Psychometric evaluations were performed during a placebo run-in phase; after a 5-day treatment period; assessments were made before, and again 1 h and 4 h after alcohol ingestion. Alcohol doses were pre-determined for each subject in order to produce a blood alcohol concentration of 0.6 g/l 1 h after alcohol intake and this individual alcohol dose was given on test days. The day before alcohol intake tests for autonomic functions were made to assess the anticholinergic effects of the drugs. Alcohol significantly increased body sway, decreased critical flicker fusion frequency, prolonged choice reaction time, impaired copying skills, impaired memory and increased the subjective feelings of satisfaction and tension. Drugs increased the effect of alcohol on body sway and this was essentially due to clomipramine. Clomipramine both without and with alcohol increased body sway, prolonged choice reaction time more than did moclobemide. Clomipramine seemed to diminish alcohol-induced memory impairment in one of the memory tests used. Subjects taking clomipramine had significantly more adverse effects after alcohol ingestion than did subjects of the moclobemide group. In contrast to moclobemide, clomipramine produced a moderate but significant drop in standing systolic blood pressure and a clear inhibition of salivary excretion.(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
Comparison of the monoamine oxidase inhibiting properties of two reversible and selective monoamine oxidase-A inhibitors moclobemide and toloxatone, and assessment of their effect on psychometric performance in healthy subjects.Br J Clin Pharmacol. 1990 Dec;30(6):805-16. doi: 10.1111/j.1365-2125.1990.tb05445.x. Br J Clin Pharmacol. 1990. PMID: 1705137 Free PMC article. Clinical Trial.
-
The effects of moclobemide on psychomotor performance and cognitive function.Int Clin Psychopharmacol. 1993 Spring;8(1):43-7. doi: 10.1097/00004850-199300810-00007. Int Clin Psychopharmacol. 1993. PMID: 8473720 Clinical Trial.
-
The effects of moclobemide on autonomic and cognitive functions in healthy volunteers.Pharmacopsychiatry. 2004 Mar;37(2):81-7. doi: 10.1055/s-2004-815530. Pharmacopsychiatry. 2004. PMID: 15048616 Clinical Trial.
-
A risk-benefit assessment of moclobemide in the treatment of depressive disorders.Drug Saf. 1995 Jan;12(1):46-54. doi: 10.2165/00002018-199512010-00004. Drug Saf. 1995. PMID: 7741983 Review.
-
The effects of moclobemide on cognition.J Neural Transm Suppl. 1989;28:91-102. J Neural Transm Suppl. 1989. PMID: 2677245 Review.
Cited by
-
Evaluation of the central effects of alcohol and caffeine interaction.Br J Clin Pharmacol. 1995 Oct;40(4):393-400. doi: 10.1111/j.1365-2125.1995.tb04562.x. Br J Clin Pharmacol. 1995. PMID: 8554942 Free PMC article. Clinical Trial.
-
Comparison of the monoamine oxidase inhibiting properties of two reversible and selective monoamine oxidase-A inhibitors moclobemide and toloxatone, and assessment of their effect on psychometric performance in healthy subjects.Br J Clin Pharmacol. 1990 Dec;30(6):805-16. doi: 10.1111/j.1365-2125.1990.tb05445.x. Br J Clin Pharmacol. 1990. PMID: 1705137 Free PMC article. Clinical Trial.
-
Behavioural toxicity of antidepressants with particular reference to moclobemide.Psychopharmacology (Berl). 1992;106 Suppl:S49-55. doi: 10.1007/BF02246236. Psychopharmacology (Berl). 1992. PMID: 1546141 Review.
-
Effects of moclobemide and mianserin on highway driving, psychometric performance and subjective parameters, relative to placebo.Psychopharmacology (Berl). 1992;106 Suppl:S62-7. doi: 10.1007/BF02246238. Psychopharmacology (Berl). 1992. PMID: 1546144 Clinical Trial.
-
Low blood alcohol concentrations and driving impairment. A review of experimental studies and international legislation.Int J Legal Med. 1994;106(4):169-77. doi: 10.1007/BF01371332. Int J Legal Med. 1994. PMID: 8038109 Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources