Adolescent Stress–Induced Epigenetic Control of Dopaminergic Neurons via Glucocorticoids
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Defeat, Distress, and Glucocorticoids: Understanding how individuals control emotions and cope with stressful events is a major clinical concern and of importance for the treatment of psychiatric illnesses (see the Perspective by McEwen ). Barik et al. (p. 332 ) discovered that aggressive defeat stress in mice caused glucocortioid release and increased activity in the dopamine system. Deleting the glucocorticoid receptors in dopaminoceptive neurons completely prevented the social avoidance that usually follows aggressive defeat. How the combination of genetic factors and environmental stressors during adolescence determines adult behavior and how their disturbance results in neuropsychiatric disorders is poorly understood. Niwa et al. (p. 335 ) found that isolation stress during adolescence, which does not cause any long-lasting changes in wild-type mice, induced significant neurochemical and behavioral alterations in mutant mice expressing a dominant-negative variant of the disrupted in schizophrenia 1 gene under the control of the prion protein promoter. These deficits could be reversed by a glucocorticoid receptor antagonist.
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In a mouse model carrying a genetic risk factor for neuropsychiatric disorders, adolescent isolation stress induces DNA hypermethylation of TH gene in mesocortical dopaminergic neurons, causing reduced TH expression and cortical dopamine release, leading to SZ-associated behavioral abnormalities.
“In a mouse model carrying a genetic risk factor for neuropsychiatric disorders, adolescent isolation stress induces DNA hypermethylation of the tyrosine hydroxylase (TH) gene in mesocortical dopaminergic neurons, causing the reduced TH expression and cortical dopamine release, leading to SZ-associated behavioral abnormalities 187.”
From Mechanisms of synaptic transmission dysregulation in the prefrontal cortex: pathophysiological implications (2022) · cites this paper as [187]
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References 41 · Cited by 318
- Authors
- Niwa, M., Jaaro-Peled, H., Tankou, S., Seshadri, S., Hikida, T., Matsumoto, Y., Cascella, N. G., Kano, S.-I., Ozaki, N., Nabeshima, T., & Sawa, A.
- Affiliations
- Johns Hopkins University (US)
- Nagoya University (JP)
- Meijo University (JP)
- Corresponding author
- Nabeshima, Toshitaka
- Sawa, Akira
- ORCID
- Venue
- Science
- Published
- 2013-01-18
- Volume
- 339
- Issue
- 6117
- Pages
- 335-339
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC3617477
- OpenAlex
- W2060969944
- Cited by
- 318
- References
- 41
- Citations by year
- 2026: 9 · 2025: 8 · 2024: 12 · 2023: 18 · 2022: 13 · 2021: 22 · 2020: 16 · 2019: 20 · 2018: 24 · 2017: 23 · 2016: 37 · 2015: 36 · 2014: 50 · 2013: 29
- FWCI
- 22.98
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Institut National de la Santé et de la Recherche Médicale
- Japan Society for the Promotion of Science (23120011, 23680034)
- National Institute of Mental Health (R21MH085226, MH084018, MH085226, RC1MH088753, MH 092443, K99MH094408, MH‑088753, P20MH084018, R01MH069853, MH-094268, P50MH094268, MH069853, R01MH092443)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Social Sciences › Psychology › Social Psychology › Neuroendocrine regulation and behavior
- Keywords
- adolescent stress, glucocorticoids, glucocorticoid receptor, dopaminergic neurons, epigenetic regulation, isolation stress, social avoidance, DISC1, dopaminergic system, neuropsychiatric disorders, glucocorticoid receptor antagonist
- MeSH terms
- Adolescent, Adolescent Behavior, Affective Disorders, Psychotic, Animals, Disease Models, Animal, Glucocorticoids, Humans, Mice, Inbred C57BL, Mice, Transgenic, Nerve Tissue Proteins, Stress, Psychological, Adolescent Development, Epigenesis, Genetic, Mice, Dopaminergic Neurons
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