Cited by 89Stress Responses and CortisolNeuroscience and Neuropharmacology ResearchTreatment of Major Depression

Chronic social defeat stress induces sustained synaptic structural changes in the prefrontal cortex and amygdala

Colyn, L., Venzala, E., Marco, S., Perez-Otaño, I., Tordera, R.M.·2019·Behavioural Brain Research

Abstract

Previous studies show that chronic stress induces synaptic structural alterations in brain regions involved in emotional processing such as the prefrontal cortex (PFC) and the basolateral amygdala (BLA). Yet, these studies are based mainly in animal exposure to unpredictable stressors or to restraint stress. On the other hand, studies using the chronic social defeat stress (CSDS), a relevant model of depression based on social conflict, are lacking. Here we aim to study the acute (24 h after CSDS) and long-term (one month after CSDS) effects of CSDS on dendritic and synaptic structures in the PFC and BLA of C57BL/6 mice. Specifically, BLA and PFC dendritic spine densities as well as BLA arborisation were analysed. Subsequently, we investigate in these regions the synaptic response to a friendly (interaction with a same strain mouse) or a fearful (interaction with a dominant strain mouse) social stimulus. Spine densities of the apical dendrites from the PFC pyramidal neurons were decreased by CSDS in the long-term (one month after CSDS). In addition, CSDS increased BLA stellate neurons spine density in the short-term (24 h after CSDS) and dendritic arborisation in the long-term. Moreover, long-term CSDS mice exposed to a fearful stimulus experienced a marked social avoidance and showed a significant increase in the expression of the immature form of the brain derived neurotrophic factor (proBDNF) in the amygdala. Taken together these results suggest the existence of persistent neuronal adaptations in the PFC and BLA in socially defeated mice. Specifically, spine density retraction in the PFC and increased BLA dendritic arborisation could represent an adaptive structural change allowing rapid expression of synaptic markers in response to fearful experiences.

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Crossref · 10.1016/j.bbr.2019.112079

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  • Cortical neuron atrophy and dysfunction is observed in rodents following chronic corticosterone administration, chronic unpredictable mild stress, chronic restraint stress, and chronic social defeat stress.

    “Cortical neuron atrophy and dysfunction is observed in rodents following chronic corticosterone administration (121), chronic unpredictable mild stress (122, 123), chronic restraint stress (48, 49, 124, 125), and chronic social defeat stress (126–128).”

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Authors
Colyn, L., Venzala, E., Marco, S., Perez-Otaño, I., & Tordera, R. M.
Affiliations
  • Universidad de Navarra (ES)
  • Centro de Investigación Médica Aplicada (ES)
Corresponding author
Tordera, R.M.
Venue
Behavioural Brain Research
Publisher
Elsevier BV
Published
2019-11
Volume
373
Pages
112079
ISSN
0166-4328 (ISSN-L)
OpenAlex
W2957263456
Cited by
89
References
6
Citations by year
2026: 7 · 2025: 16 · 2024: 11 · 2023: 18 · 2022: 14 · 2021: 12 · 2020: 7 · 2019: 3
FWCI
5.90
Type
journal article
Language
en
Open access
closed
Locations
  • Behavioural Brain Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Ministry of Science and Innovation (SAF2011-27910)
  • PIUNA (University of Navarra)
Topics
  • Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
Keywords
chronic social defeat stress, depression, prefrontal cortex, basolateral amygdala, dendritic spine density, dendritic branching, synaptic plasticity, social avoidance, proBDNF, stellate neurons, pyramidal neurons, social conflict, emotional processing
MeSH terms
Amygdala, Animals, Behavior, Animal, Brain, Dendrites, Depression, Depressive Disorder, Male, Mice, Inbred C57BL, Synaptic Transmission, Neuronal Plasticity, Neurons, Social Behavior, Stress, Psychological, Synapses, Prefrontal Cortex, Pyramidal Cells, Dendritic Spines, Mice, Basolateral Nuclear Complex

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