Neuronal damage and protection in the pathophysiology and treatment of psychiatric illness: stress and depression
Open accessAbstract
The discovery that stress and depression, as well as other psychiatric illnesses, are characterized by structural alterations, and that these changes result from atrophy and loss of neurons and glia in specific limbic regions and circuits, has contributed to a fundamental change in our understanding of these illnesses. These structural changes are accompanied by dysregulation of neuroprotective and neurotrophic signaling mechanisms that are required for the maturation, growth, and survival of neurons and glia. Conversely, behavioral and therapeutic interventions can reverse these structural alterations by stimulating neuroprotective and neurotrophic pathways and by blocking the damaging, excitotoxic, and inflammatory effects of stress. Lifetime exposure to cellular and environmental stressors and interactions with genetic factors contribute to individual susceptibility or resilience. This exciting area of research holds promise and potential for further elucidating the pathophysiology of psychiatric illness and for development of novel therapeutic interventions.
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There is some evidence that neuronal damage may occur in major depression, suggesting that DAMPs may also have a role in the pathophysiology of depression.
“there is some evidence that neuronal damage may occur in major depression (Duman, 2009), suggesting that DAMPs may also have a role in the pathophysiology of depression.”
From Danger Signals and Inflammasomes: Stress-Evoked Sterile Inflammation in Mood Disorders (2017) · cites this paper as Duman, 2009
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References 189 · Cited by 210
Research works printed but not linked: 1
- [184]Koo J. Duman RS. IL-1B is an essential mediator of the anti-neurogenic and anhedonic effects of sress. Soc Neurosci Abst. 2008 105 751 756 PMC2206608 18178625
- Authors
- Duman, R. S.
- Affiliations
- Yale University (US)
- Corresponding author
- Duman, Ronald S.
- ORCID
- Duman, Ronald S.
- Venue
- Dialogues in Clinical Neuroscience
- Publisher
- Informa UK Limited
- Published
- 2009-09-30
- Volume
- 11
- Issue
- 3
- Pages
- 239-255
- ISSN
- 1294-8322 (ISSN-L)
- 1958-5969
- PMC
- PMC3181922
- OpenAlex
- W1546686332
- Cited by
- 210
- References
- 189
- Citations by year
- 2026: 3 · 2025: 11 · 2024: 11 · 2023: 9 · 2022: 17 · 2021: 18 · 2020: 7 · 2019: 8 · 2018: 9 · 2017: 9 · 2016: 16 · 2015: 20 · 2014: 8 · 2013: 25 · 2012: 21
- FWCI
- 4.62
- Type
- journal article
- Language
- en
- Open access
- diamond
- doi.org
- Licence
- Locations
- Dialogues in Clinical Neuroscience (publishedVersion, cc-by-nc-nd)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- Funders
- National Institute of Mental Health (MH-45481, R37MH045481, P01MH025642, R01MH045481)
- Topics
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
- Keywords
- neuronal injury, neuroprotection, neurotrophic signaling, stress, depression, neuronal atrophy, limbic system, excitotoxicity, neuroinflammation, resilience, genetic susceptibility, neurotrophic therapy
- MeSH terms
- Animals, Depression, Disease Models, Animal, Humans, Models, Biological, Neuronal Plasticity, Neurons, Stress, Psychological, Signal Transduction, Neuroprotective Agents, Brain-Derived Neurotrophic Factor
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