Literature DB >> 25139739

Effects of negative stressors on DNA methylation in the brain: implications for mood and anxiety disorders.

Benjamin Hing1, Caleb Gardner, James B Potash.   

Abstract

Stress is a major contributor to anxiety and mood disorders. The recent discovery of epigenetic changes in the brain resulting from stress has enhanced our understanding of the mechanism by which stress is able to promote these disorders. Although epigenetics encompasses chemical modifications that occur at both DNA and histones, much attention has been focused on stress-induced DNA methylation changes on behavior. Here, we review the effect of stress-induced DNA methylation changes on physiological mechanisms that govern behavior and cognition, dysregulation of which can be harmful to mental health. A literature review was performed in the areas of DNA methylation, stress, and their impact on the brain and psychiatric illness. Key findings center on genes involved in the hypothalamic-pituitary-adrenal axis, neurotransmission and neuroplasticity. Using animal models of different stress paradigms and clinical studies, we detail how DNA methylation changes to these genes can alter physiological mechanisms that influence behavior. Appropriate levels of gene expression in the brain play an important role in mental health. This dynamic control can be disrupted by stress-induced changes to DNA methylation patterns. Advancement in other areas of epigenetics, such as histone modifications and the discovery of the novel DNA epigenetic mark, 5-hydroxymethylcytosine, could provide additional avenues to consider when determining the epigenetic effects of stress on the brain.
© 2014 Wiley Periodicals, Inc.

Entities:  

Keywords:  DNA methylation; HPA axis; genome-wide DNA methylation; neuroplasticity; neurotransmission

Mesh:

Year:  2014        PMID: 25139739      PMCID: PMC5096645          DOI: 10.1002/ajmg.b.32265

Source DB:  PubMed          Journal:  Am J Med Genet B Neuropsychiatr Genet        ISSN: 1552-4841            Impact factor:   3.568


  142 in total

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2.  Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a.

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3.  Childhood family violence and adult recurrent depression.

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4.  Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene.

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7.  Life events and the course of bipolar disorder.

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Journal:  Am J Psychiatry       Date:  1990-09       Impact factor: 18.112

8.  Neuronal cell-type specific DNA methylation patterns of the Cacna1c gene.

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10.  The different roles of glucocorticoids in the hippocampus and hypothalamus in chronic stress-induced HPA axis hyperactivity.

Authors:  Li-Juan Zhu; Meng-Ying Liu; Huan Li; Xiao Liu; Chen Chen; Zhou Han; Hai-Yin Wu; Xing Jing; Hai-Hui Zhou; Hoonkyo Suh; Dong-Ya Zhu; Qi-Gang Zhou
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  9 in total

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2.  Epigenetics, Media Coverage, and Parent Responsibilities in the Post-Genomic Era.

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Journal:  Curr Genet Med Rep       Date:  2016-06-14

3.  Impact of DNMT1 and DNMT3a forebrain knockout on depressive- and anxiety like behavior in mice.

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Review 4.  Epigenetics of Stress, Addiction, and Resilience: Therapeutic Implications.

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Journal:  Mol Neurobiol       Date:  2014-12-11       Impact factor: 5.590

Review 5.  Understanding Epigenetics in the Neurodegeneration of Alzheimer's Disease: SAMP8 Mouse Model.

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Journal:  J Alzheimers Dis       Date:  2018       Impact factor: 4.472

6.  DNA methylation in adolescents with anxiety disorder: a longitudinal study.

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7.  Longitudinal DNA methylation changes at MET may alter HGF/c-MET signalling in adolescents at risk for depression.

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8.  The early-life exposome modulates the effect of polymorphic inversions on DNA methylation.

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9.  Persistent inflammatory pain is linked with anxiety-like behaviors, increased blood corticosterone, and reduced global DNA methylation in the rat amygdala.

Authors:  Richard L Spinieli; Rafael Alves Cazuza; Amanda Juliana Sales; Ruither Oliveira Gomes Carolino; Diana Martinez; Janete Anselmo-Franci; Maral Tajerian; Christie Ra Leite-Panissi
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  9 in total

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