| Literature DB >> 27781556 |
Ioline D Henter1, Rafael T de Sousa1, Philip W Gold1, Andre R Brunoni2, Carlos A Zarate1, Rodrigo Machado-Vieira1.
Abstract
INTRODUCTION: Real-world effectiveness trials suggest that antidepressant efficacy is limited in many patients with mood disorders, underscoring the urgent need for novel therapeutics to treat these disorders. Areas covered: Here, we review the clinical evidence supporting the use of novel modulators for the treatment of mood disorders, including specific glutamate modulators such as: 1) high-trapping glutamatergic modulators; 2) subunit (NR2B)-specific N-methyl-D-aspartate (NMDA) receptor antagonists; 3) NMDA receptor glycine-site partial agonists; and 4) metabotropic glutamate receptor (mGluR) modulators. We also discuss other promising, non-glutamatergic targets for potential rapid antidepressant effects in mood disorders, including the cholinergic system, the glucocorticoid system, and the inflammation pathway, as well as several additional targets of interest. Clinical evidence is emphasized, and non-pharmacological somatic treatments are not reviewed. In general, this paper only explores agents available in the United States. Expert commentary: Of these novel targets, the most promising - and the ones for whom the most evidence exists - appear to be the ionotropic glutamate receptors. However, moving forward will require us to fully embrace the goal of personalized medicine and will require health professionals to pre-emptively identify potential responders.Entities:
Keywords: AMPA receptor; N-methyl-D-aspartate (NMDA); bipolar disorder; depression; glutamate; major depressive disorder (MDD); mood; treatment
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Year: 2017 PMID: 27781556 PMCID: PMC5552063 DOI: 10.1080/17512433.2017.1253472
Source DB: PubMed Journal: Expert Rev Clin Pharmacol ISSN: 1751-2433 Impact factor: 5.045