Summary
An open study was carried out to examine the effect of moclobemide, a new antidepressant reversible inhibitor of MAO-A, on the pressor response induced by oral tyramine added to meals of different lipid and protein composition, and to correlate the blood pressure increase in the tyramine test with that obtained during an exercise test.
Eight healthy volunteers of both sexes participated in the study. A tyramine sensitivity and an exercise test were performed beforehand. Subjects were included if, under fasting condition, their systolic blood pressure (SBP) increased by more than 30 mmHg after administration of 400 or 600 mg tyramine. Exercise tests were performed to determine the grade of effort that corresponded to a rise in SBP of 30 mmHg.
Subjects received moclobemide 600 mg/d. Starting on Day 7, each subject consumed a standardized meal (52 g lipids, 43 g proteins, 86 g carbohydrates) just before taking moclobemide. Tyramine was added to these meals in daily increasing doses of 50, 100, 150 ... mg until an increase in SBP > 30 mmHg was obtained. On moclobemide treatment, an average dose of 250 mg tyramine (range 150-400 mg) increased SBP by 36.6 mmHg. The time to reach peak SBP was longer (175 min) than in the fasting condition before the trial (40.6 min).
The administration of the same dose of tyramine both during a protein-rich (75 g proteins, 85 g lipids, 90 g carbohydrates) and lipid-rich (110 g lipids, 55 g proteins, 100 g carbohydrates) meal significantly reduced the average increase in SBP to 21 mmHg, but did not significantly modify the time of appearance of the peak SBP
In the exercise test, an increase in SBP of 30 mmHg was produced by the low load of about 100 W. During moclobemide treatment, oral doses of tyramine considerably larger than the amounts present in normal meals did not increase SBP by more than the effort exerted during every day life. Concomitant administration of a large quantity of lipids significantly reduced the pressor response.
Similar content being viewed by others
References
Berlin I, Zimmer R, Cournot A, Payan C, Pedarriosse AM, Puech AJ (1989) Determination and comparison of the pressor effect of tyramine during long term moclobemide and tranylcypromine treatment in healthy volunteers. Clin Pharmacol Ther 46:344–351
Blackwell B, Marley E (1966) Hypertensive interactions between MAGI and foodstuffs. In: Brill H, Cole JO, Deniker P, Hippius H, Bradley PB (eds) Proceedings of the Vth International Congress of Neuro-Psycho-Pharmacology, Excerpta Medica, Amsterdam, pp 558–587
Burn JH, Rand MJ (1958) The action of sympathomimetic amines in animals treated with reserpine. J Physiol (London) 144: 314–336
Dajas F, Lista A, Barbeito L (1984) High urinary norepinephrine excretion in major depressive disorders: effects of a new type of MAO inhibitor (moclobemide, Ro 11-1163) Acta Psychiatr Scand 275:1–6
Da Prada M, Zurcher G, Wuthrich I, Haefety WE (1988) On tyramine, food, beverages and the reversible MAO inhibitor moclobemide. J Neural Transm [Suppl] 26:31–56
Goridis C, Neff NH (1971) Monoamine oxidase in sympathetic nerves: a transmitter specific enzyme type. Br J Pharmacol 43:814–818
Grind M, Siwers B, Graffner C, Alvan G, Gustafsson LL, Halleday J, Lingren JE, Ogenstad S, Selander H (1986) Pressor response of oral tyramine in healthy men given amiflamine and placebo. Clin Pharmacol Ther 40:155–160
Guentert TW, Tucker G, Korn A, Pfefen JP, Haefelfinger P, Schoerlin MP (1990) Pharmacokinetics of moclobemide after single and multiple oral dosing with 150 milligrams 3 times daily for 15 days. Acta Psychiatr Scand 82 [Suppl 360]:91–93
Houslay MD, Tipton KF, Youdim MBH (1971) Multiple forms of monoamine oxidase, fact and artefact. Life Sci 19:467–478
Korn A, Eichler HE, Fischbach R, Gasic S (1986) Moclobemide, a new reversible MAO-inhibitor-interaction with tyramine and tricyclic antidepressants in healthy volunteers and depressive patients. Psychopharmacology 88:153–157
Korn A, Da Prada M, Raffesberg W, Gasic S, Eichler HG (1988) Effect of moclobemide, a new reversible monoamine oxidase inhibitor, on absorption and pressor effect of tyramine. J Cardiovasc Pharmacol 11:17–23
Larsen JK, Holm P, Mikkelsen PL (1984) Moclobemide and clomipramine in the treatment of depression. Acta Psychiatr Scand 70:254–260
Lecrubier Y, Guelfi JD (1990) Efficacy of reversible inhibitors of monoamine oxidase A in various forms of depression. Acta Psychiatr Scand 82 [Suppl 360]:18–23
Marley E, Blackwell B (1970) Interactions of monoamine oxidase inhibitors, amines and foodstuffs. Adv Pharmacol Chemother 8:185–239
Martini A, Bonollo L, Nicolis FB, Sega R, Palermo A (1981) Effects of caroxazone, a reversible monoamine oxidase inhibitor, on the pressor response to oral tyramine in man. Br J Clin Pharmacol 11:611–615
Norman TR, Ames D, Burrows GD, Davies B (1985) A controlled study of a specific MAO A reversible inhibitor (Ro 11-1163) and Amitriptyline in depressive illness. J Affect Disorders 8:29–35
Schoerlin MP, Mayersohn M, Hoevels B, Eggers H, Dellenbach M, Pfefen JP (1988) Effect of food intake on relative bioavailability of moclobemide (Ro 11-1163). J Neural Transm Suppl 26:115–121
Schulz R, Bieck PR (1987) Oral tyramine pressor test and the safety of MAO inhibitor drugs. Psychopharmacology 91:515–516
Simpson GM, White K (1984) Tyramine studies and the safety of MAGI drugs. J Clin Psychiatry 45:59–61
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Audebert, C., Blint, O., Monjanel-Mouterde, S. et al. Influence of food on the tyramine pressor effect during chronic moclobemide treatment of healthy volunteers. Eur J Clin Pharmacol 43, 507–512 (1992). https://doi.org/10.1007/BF02285092
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF02285092