Cited by 210Stress Responses and CortisolTreatment of Major DepressionTryptophan and brain disorders

Neuronal damage and protection in the pathophysiology and treatment of psychiatric illness: stress and depression

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Duman, Ronald S.·2009·Dialogues in Clinical Neuroscience

Abstract

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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Crossref · 10.31887/dcns.2009.11.3/rsduman

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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.”

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References 189 · Cited by 210

Research works printed but not linked: 1

  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.
Venue
Dialogues in Clinical Neuroscience
Published
2009-09-30
Volume
11
Issue
3
Pages
239-255
ISSN
  • 1294-8322 (ISSN-L)
  • 1958-5969
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
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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