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Eur J Pharmacol ; 752: 49-54, 2015 Apr 05.
Article in English | MEDLINE | ID: mdl-25661848

ABSTRACT

A great deal of evidence suggests that virtually all antidepressant treatments induce a dopaminergic behavioral supersensitivity. We have suggested that this effect may play a key role not only in the antidepressant effect of these treatments, but also in their ability to induce a switch from depression to mania. In 2003-4 we found that the sensitization of dopamine receptors induced by imipramine is followed, after imipramine withdrawal, by a desensitization of these receptors associated with a depressive-like behavior assessed in the forced swimming test. The dopamine receptor sensitization can be prevented by MK-801, an NMDA receptor antagonist, but not by currently used mood stabilizers (lithium, carbamazepine, valproate). These observations led us to suggest - and later confirm - with preliminary clinical observations that memantine may have an acute antimanic and a long-lasting mood-stabilizing effect in treatment-resistant bipolar disorder patients. Here we present data showing that memantine prevents not only the dopamine receptor sensitization induced by imipramine, as observed with MK-801, but also the ensuing desensitization and the associated depressive-like behaviorq observed after antidepressant withdrawal.


Subject(s)
Antidepressive Agents/adverse effects , Behavior, Animal/drug effects , Bipolar Disorder/chemically induced , Bipolar Disorder/prevention & control , Imipramine/adverse effects , Memantine/pharmacology , Animals , Antidepressive Agents/therapeutic use , Bipolar Disorder/metabolism , Depression/drug therapy , Depression/metabolism , Imipramine/therapeutic use , Male , Rats , Rats, Sprague-Dawley , Receptors, Dopamine/metabolism , Swimming , Time Factors
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