Evaluation of VU0409106 in preclinical models of Major Depressive Disorder

Vanderbilt University, Nashville TN

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Abstract

Major depressive disorder (MDD) is a debilitating psychiatric illness that affects approximately 16% of the population worldwide and is associated with symptoms of depressed mood and anhedonia. Currently available antidepressant therapies, which work through enhancement of synaptic biogenic amine levels, provide limited symptomatic remission and are associated with delayed onset of action and dose-limiting side-effects in MDD patients. Recent clinical findings with antagonists of the N-methyl-D-aspartate subtype of glutamate receptor (NMDAR) have reported robust and rapid efficacy in patients with MDD, particularly in treatment resistant populations. However, these direct-acting NMDAR antagonists are also associated with adverse side-effects that limit their clinical utility. Alternatively, the metabotropic glutamate receptor subtype 5 (mGluRs) is a close downstream signaling partner of the NMDAR; and antagonism of mGluRs results in inhibition of NMDAR signaling suggesting that mGluRs antagonists may provide an exciting new approach for the treatment of MDD. Recently, our group has been successful in the development of a highly selective series of mGluRs negative allosteric modulators (NAM), represented by VU0409106, that are now optimized as novel in vivo tools for further validation of the potential for mGluRs NAMs in MDD. In project 1 of this NCDDG, we will evaluate VU0409106 in several well established preclinical models of antidepressant-like activity and establish the degree of target engagement of central mGluRs necessary to observe efficacy using the selective mGluRs radiolig and [ [3]H]m-PEPy. We will also evaluate the effects of VU0409106 in several preclinical models of anhedonia, which may be more relevant for evaluating novel mechanisms for antidepressant effects. Finally, we will assess the potential for VU0409106 to produce adverse effects associated with excessive NMDAR antagonism to establish the therapeutic index for the mechanism of this ligand.