Literature DB >> 20018197

From synapse to nucleus: novel targets for treating depression.

Herbert E Covington1, Vincent Vialou, Eric J Nestler.   

Abstract

The need for newer compounds to treat depression is an ever-growing concern due to the enormous societal and financial ramifications of this disorder. Here, we review some of the candidate systems that could potentially be involved in depression, or an inherent resistance to depression termed resilience, and the numerous protein targets for these systems. A substantial body of literature provides strong evidence that neurotrophic factors, glutamate receptors, hypothalamic feeding peptides, nuclear hormone receptors, and epigenetic mechanisms, among others, will make for interesting targets when examining depressive behavior or resilience in preclinical models, and eventually clinical trials. Although some of these targets for depression already appear promising, new waves of more selective compounds for any molecular system should promote a better understanding of this complex disease and perhaps improved treatments. Copyright 2009 Elsevier Ltd. All rights reserved.

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Year:  2009        PMID: 20018197      PMCID: PMC2821954          DOI: 10.1016/j.neuropharm.2009.12.004

Source DB:  PubMed          Journal:  Neuropharmacology        ISSN: 0028-3908            Impact factor:   5.250


  158 in total

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