Epigenetic mechanisms of major depression: Targeting neuronal plasticity

被引:118
|
作者
Uchida, Shusaku [1 ,2 ]
Yamagata, Hirotaka [1 ,2 ]
Seki, Tomoe [1 ,2 ]
Watanabe, Yoshifumi [1 ]
机构
[1] Yamaguchi Univ, Grad Sch Med, Dept Neurosci, Div Neuropsychiat, 1-1-1 Minami Kogushi, Ube, Yamaguchi 7558505, Japan
[2] Japan Sci & Technol Agcy, Core Res Evolut Sci & Technol, Kawaguchi, Saitama, Japan
关键词
depression; DNA methylation; histone acetylation; non-coding RNA; stress; HISTONE DEACETYLASE INHIBITORS; NATIONAL-COMORBIDITY-SURVEY; SEROTONIN TRANSPORTER GENE; BDNF PROMOTER METHYLATION; EARLY-LIFE ADVERSITY; LONG-TERM-MEMORY; SYNAPTIC PLASTICITY; PSYCHIATRIC-DISORDERS; DNA METHYLATION; PREFRONTAL CORTEX;
D O I
10.1111/pcn.12621
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Major depressive disorder is one of the most common mental illnesses as it affects more than 350 million people globally. Major depressive disorder is etiologically complex and disabling. Genetic factors play a role in the etiology of major depression. However, identical twin studies have shown high rates of discordance, indicating non-genetic mechanisms as well. For instance, stressful life events increase the risk of depression. Environmental stressors also induce stable changes in gene expression within the brain that may lead to maladaptive neuronal plasticity in regions implicated in disease pathogenesis. Epigenetic events alter the chromatin structure and thus modulate expression of genes that play a role in neuronal plasticity, behavioral response to stress, depressive behaviors, and response to antidepressants. Here, we review new information regarding current understanding of epigenetic events that may impact depression. In particular, we discuss the roles of histone acetylation, DNA methylation, and non-coding RNA. These novel mechanisms of action may lead to new therapeutic strategies for treating major depression.
引用
收藏
页码:212 / 227
页数:16
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