Literature DB >> 22691453

Environmental and pharmacological modulations of cellular plasticity: role in the pathophysiology and treatment of depression.

Kristie T Ota1, Ronald S Duman.   

Abstract

Atrophy of neurons and gross structural alterations of limbic brain regions, including the prefrontal cortex (PFC) and hippocampus, have been reported in brain imaging and postmortem studies of depressed patients. Preclinical findings have suggested that prolonged negative stress can induce changes comparable to those seen in major depressive disorder (MDD), through dendritic retraction and decreased spine density in PFC and hippocampal CA3 pyramidal neurons. Interestingly, recent studies have suggested that environmental and pharmacological manipulations, including antidepressant medication, exercise, and diet, can block or even reverse many of the molecular changes induced by stress, providing a clear link between these factors and susceptibility to MDD. In this review, we will discuss the environmental and pharmacological factors, as well as the contribution of genetic polymorphisms, involved in the regulation of neuronal morphology and plasticity in MDD and preclinical stress models. In particular, we will highlight the pro-depressive changes incurred by stress and the reversal of these changes by antidepressants, exercise, and diet. 2012 Elsevier Inc. All rights reserved

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Year:  2012        PMID: 22691453      PMCID: PMC3458126          DOI: 10.1016/j.nbd.2012.05.022

Source DB:  PubMed          Journal:  Neurobiol Dis        ISSN: 0969-9961            Impact factor:   5.996


  209 in total

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2.  A role for MAP kinase signaling in behavioral models of depression and antidepressant treatment.

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6.  Gene-environment interaction analysis of serotonin system markers with adolescent depression.

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Review 9.  A neural signaling triumvirate that influences ageing and age-related disease: insulin/IGF-1, BDNF and serotonin.

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  36 in total

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6.  The guanine nucleotide exchange factor (GEF) Asef2 promotes dendritic spine formation via Rac activation and spinophilin-dependent targeting.

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Review 7.  Pathogenetic and therapeutic applications of microRNAs in major depressive disorder.

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Review 8.  Targeting opioid dysregulation in depression for the development of novel therapeutics.

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