Article ID Journal Published Year Pages File Type
2011351 Pharmacological Reports 2013 7 Pages PDF
Abstract

BackgroundThe involvement of glutamate system (particularly the NMDAand AMPAreceptors) in the mechanism of antidepressant activity was demonstrated in preclinical and clinical studies.MethodsIn the present study, we investigated the effect of NMDAand AMPAreceptors’ ligands (agonists and antagonists) on the antidepressant-like activity of escitalopram, milnacipran, imipramine and reboxetine in the forced swim test in mice.ResultsAntidepressant activity (reduction in immobility time) of escitalopram and milnacipran but not of imipramine and reboxetine was antagonized by N-methyl-D-aspartate acid. CGP37849 (antagonist of the NMDAreceptor) enhanced the antidepressant activity of all examined antidepressants. On the other hand, CX614 (a potentiator/positive allosteric modulator of the AMPAreceptor) enhanced the antidepressant activity of imipramine and reboxetine but not of escitalopram and milnacipran in this test. NBQX (the AMPA receptor antagonist) did not influence the antidepressant activity of all tested agents.ConclusionsThe data indicate the complex interactions following the activation or blockade of theNMDAandAMPAreceptors with antidepressant drugs. The general phenomenon is the enhancing effect of the NMDAreceptor antagonism on the antidepressant activity. Moreover, is can be concluded that the activity of antidepressants with a serotonergic mechanism of action can be inhibited by NMDA activation, while antidepressants with a noradrenergic mechanism of action are dependent on AMPA receptor transmission.

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