The use of monoamine oxidase inhibitors (MA01s) in the treatment of de
pression has been bedeviled by reports of potentially dangerous or eve
n fatal interactions with dietary amines and other drugs together with
reports of more conventional toxicity to organs such as the liver. As
a result, these otherwise very important and useful drugs have not be
en employed clinically as much as their effectiveness as antidepressan
ts would indicate. Many of these unwanted actions were due partially o
r entirely to the fact that the older MAOIs all inhibited MAO irrevers
ibly. The introduction of reversible inhibitors of monoamine oxidase-A
(RIMAs) has greatly reduced both the number and severity of these int
eractions and, in particular, the risk of hypertensive crises followin
g the ingestion of tyramine (the ''cheese effect''). Potential interac
tions may remain with inhibitors of the uptake of 5-hydroxytryptamine,
including pethidine and rapid release formulations of nasal decongest
ant amines. Potential interactions between RIMAs and other drugs that
compete for the same metabolic pathways may still occur but should onl
y result in changes in duration of action.