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bioRxiv · 10.1101/2024.03.28.587210

Resting-state fMRI reveals altered functional connectivity associated with resilience and susceptibility to chronic social defeat stress in mouse brain

Abstract

Chronic stress is a causal antecedent condition for major depressive disorder and associates with altered patterns of neural connectivity. There are nevertheless important individual differences in susceptibility to chronic stress. How stress-induced alterations in functional connectivity amongst depression-related brain regions associates with resilience and susceptibility to chronic stress is largely unknown. We used resting-state functional magnetic resonance imaging (rs-fMRI) to examine functional connectivity between established depression-related regions in susceptible (SUS) and resilient (RES) adult mice following chronic social defeat stress (CSDS). Seed-seed FC analysis revealed that the ventral dentate gyrus (vDG) exhibited the greatest number of group differences in functional connectivity with targeted brain regions. SUS mice showed greater functional connectivity between the vDG and subcortical regions compared to both control (CON) or RES groups. Whole brain vDG seed-voxel analysis supported seed-seed findings in SUS mice and indicated significantly decreased connectivity between the vDG and anterior cingulate area compared to CON mice. Interestingly, RES mice exhibited enhanced connectivity between the vDG and anterior cingulate area compared to SUS mice. Moreover, RES mice showed greater connectivity between the infralimbic prefrontal cortex and the nucleus accumbens shell. These findings indicate unique differences in functional connectivity patterns in SUS and RES mice that could represent a neurobiological basis for vulnerability for stress-induced depression.

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BibTeXRIS

Parent, C., Lupinsky, D., Nasseef, T., Craig, K., Diorio, J., Zhang, T. Y., Meaney, M. J.. 2024-03-30. Resting-state fMRI reveals altered functional connectivity associated with resilience and susceptibility to chronic social defeat stress in mouse brain. https://doi.org/10.1101/2024.03.28.587210

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