» Articles » PMID: 37690044

Social Isolation Leads to Mild Social Recognition Impairment and Losses in Brain Cellularity

Overview
Specialty Neurology
Date 2023 Sep 10
PMID 37690044
Authors
Affiliations
Soon will be listed here.
Abstract

Chronic social stress is a significant risk factor for several neuropsychiatric disorders, mainly major depressive disorder (MDD). In this way, patients with clinical depression may display many symptoms, including disrupted social behavior and anxiety. However, like many other psychiatric diseases, MDD has a very complex etiology and pathophysiology. Because social isolation is one of the multiple depression-inducing factors in humans, this study aims to understand better the link between social stress and MDD using an animal model based on social isolation after weaning, which is known to produce social stress in mice. We focused on cellular composition and white matter integrity to establish possible links with the abnormal social behavior that rodents isolated after weaning displayed in the three-chamber social approach and recognition tests. We used the isotropic fractionator method to assess brain cellularity, which allows us to robustly estimate the number of oligodendrocytes and neurons in dissected brain regions. In addition, diffusion tensor imaging (DTI) was employed to analyze white matter microstructure. Results have shown that post-weaning social isolation impairs social recognition and reduces the number of neurons and oligodendrocytes in important brain regions involved in social behavior, such as the anterior neocortex and the olfactory bulb. Despite the limitations of animal models of psychological traits, evidence suggests that behavioral impairments observed in patients might have similar biological underpinnings.

Citing Articles

Social and nonsocial environmental loss have differential effects on ventral hippocampus-dependent behavior and inhibitory synaptic markers in adult male mice.

Gore I, Brown C, Waters R, Gould E Learn Mem. 2024; 31(12).

PMID: 39681456 PMC: 11662144. DOI: 10.1101/lm.053968.124.

References
1.
Banasr M, Duman R . Glial loss in the prefrontal cortex is sufficient to induce depressive-like behaviors. Biol Psychiatry. 2008; 64(10):863-70. PMC: 2709733. DOI: 10.1016/j.biopsych.2008.06.008. View

2.
Banasr M, Dwyer J, Duman R . Cell atrophy and loss in depression: reversal by antidepressant treatment. Curr Opin Cell Biol. 2011; 23(6):730-7. PMC: 3259683. DOI: 10.1016/j.ceb.2011.09.002. View

3.
Begni V, Sanson A, Pfeiffer N, Brandwein C, Inta D, Talbot S . Social isolation in rats: Effects on animal welfare and molecular markers for neuroplasticity. PLoS One. 2020; 15(10):e0240439. PMC: 7591026. DOI: 10.1371/journal.pone.0240439. View

4.
Belzung C, Griebel G . Measuring normal and pathological anxiety-like behaviour in mice: a review. Behav Brain Res. 2001; 125(1-2):141-9. DOI: 10.1016/s0166-4328(01)00291-1. View

5.
Bielsky I, Young L . Oxytocin, vasopressin, and social recognition in mammals. Peptides. 2004; 25(9):1565-74. DOI: 10.1016/j.peptides.2004.05.019. View