Epigenetic signaling in psychiatric disorders: stress and depression
Open accessAbstract
Psychiatric disorders are complex multifactorial disorders involving chronic alterations in neural circuit structure and function. While genetic factors play a role in the etiology of disorders such as depression, addiction, and schizophrenia, relatively high rates of discordance among identical twins clearly point to the importance of additional factors. Environmental factors, such as stress, play a major role in the psychiatric disorders by inducing stable changes in gene expression, neural circuit function, and ultimately behavior. Insults at the developmental stage and in adulthood appear to induce distinct maladaptations. Increasing evidence indicates that these sustained abnormalities are maintained by epigenetic modifications in specific brain regions. Indeed, transcriptional dysregulation and associated aberrant epigenetic regulation is a unifying theme in psychiatric disorders. Aspects of depression can be modeled in animals by inducing disease-like states through environmental manipulations, and these studies can provide a more general understanding of epigenetic mechanisms in psychiatric disorders. Understanding how environmental factors recruit the epigenetic machinery in animal models is providing new insights into disease mechanisms in humans.
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There are functional interactions between DNA methylation and metabolic/stress pathways.
“indicating functional interactions between DNA methylation and metabolic/stress pathways (Bagot et al., 2014; Sun et al., 2013)”
From Histone modifications and depression: epigenetic mechanisms, therapeutic targets, and translational outlook (2026) · cites this paper as Bagot et al., 2014
The ‘Prenatal stress’ subsection of ‘DNA methylation’ (page unavailable) describes stress-associated methylation of Hsd11b2, a gene involved in glucocorticoid conversion, and says this may affect enzyme activity and offspring stress responses. That supports a possible functional link to a stress-related metabolic process, but not an established interaction with metabolic pathways more broadly. (LLM, conf=0.78)
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References 105 · Cited by 171
- Authors
- Bagot, R. C., Labonté, B., Peña, C. J., & Nestler, E. J.
- Affiliations
- Icahn School of Medicine at Mount Sinai (US)
- Fishberg Department of Neuroscience and Friedman Brain Institute, Icahn School of Medicine at Mount Sinai, New York, New York, USA
- Corresponding author
- Nestler, Eric J.
- Venue
- Dialogues in Clinical Neuroscience
- Publisher
- Informa UK Limited
- Published
- 2014-09-30
- Volume
- 16
- Issue
- 3
- Pages
- 281-295
- ISSN
- 1294-8322 (ISSN-L)
- 1958-5969
- PMC
- PMC4214172
- OpenAlex
- W2129161558
- Cited by
- 171
- References
- 105
- Citations by year
- 2026: 9 · 2025: 7 · 2024: 8 · 2023: 17 · 2022: 10 · 2021: 19 · 2020: 15 · 2019: 21 · 2018: 16 · 2017: 17 · 2016: 20 · 2015: 12
- FWCI
- 6.69
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- Locations
- Dialogues in Clinical Neuroscience (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (P50MH096890, R01MH051399)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- epigenetic signaling, depression, stress, mental illness, environmental factors, gene expression, neural circuit function, transcriptional dysregulation, animal models of depression
- MeSH terms
- Depression, Humans, Stress, Psychological, Signal Transduction, Gene Expression, Epigenesis, Genetic
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