Behavioral effects of phenelzine in an experimental model for screening
anxiolytic and anti-panic drugs: correlation with changes in monoamine-oxidase
activity and monoamine levels
by
Griebel G, Curet O, Perrault G, Sanger DJ
Synthelabo Recherche, Bagneux, France.
ggriebel@compuserve.com
Neuropharmacology 1998 Jul; 37(7):927-35
ABSTRACT
This study investigated the effects of acute and chronic (one daily i.p.
injection for 14 days) treatments with the non-selective irreversible
monoamine-oxidase (MAO) inhibitor phenelzine (10 and 30 mg/kg) on defensive
behaviors of Swiss mice in the mouse defense test battery (MDTB) which has been
designed for screening anxiolytic and anti-panic drugs. In the MDTB, subjects
were confronted with a natural threat (a rat) and situations associated with
this threat. MAO-A and MAO-B activities and levels of brain monoamines
(serotonin (5-HT), dopamine (DA) and norepinephrine (NE)) and their deaminated
metabolites were subsequently measured. Behavioral results showed that acute
administration of phenelzine did not specifically modify defensive behaviors. By
contrast, after chronic treatment, phenelzine produced a significant reduction
in avoidance distance when the rat was approaching, an effect which is
consistent with an anti-panic-like action. In addition, phenelzine displayed
weak anxiolytic-like effects as it increased risk assessment responses when mice
were constrained in one part of the apparatus facing the rat which remained at a
constant distance. No other specific drug effect was observed. These behavioral
changes were associated with a dramatic increase in 5-HT levels, in particular
after chronic treatment, while levels of DA and NE increased only slightly.
Importantly, no significant differences in DA and NE levels between acute and
chronic regimens were observed. Levels of deaminated metabolites of monoamines
were markedly decreased. Measurements of MAO activity revealed substantial
reductions in both type A and B forms with a full inhibition of both forms being
observed only after chronic treatment with phenelzine. These results suggest
that the effects of phenelzine may be due mainly to its effects on the 5-HT
system and presumably related to the full inhibition of MAO-A and/or MAO-B.
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