Abstract

The socially monogamous prairie vole (Microtus ochrogaster) offers a unique opportunity to examine the impacts of adolescent social isolation on the brain, immune system, and behavior. In the current study, male and female prairie voles were randomly assigned to be housed alone or with a same-sex cagemate after weaning (i.e., on postnatal day 21–22) for a 6-week period. Thereafter, subjects were tested for anxiety-like and depressive-like behaviors using the elevated plus maze (EPM) and Forced Swim Test (FST), respectively. Blood was collected to measure peripheral cytokine levels, and brain tissue was processed for microglial density in various brain regions, including the Nucleus Accumbens (NAcc), Medial Amygdala (MeA), Central Amygdala (CeA), Bed Nucleus of the Stria Terminalis (BNST), and Paraventricular Nucleus of the Hypothalamus (PVN). Sex differences were found in EPM and FST behaviors, where male voles had significantly lower total arm entries in the EPM as well as lower latency to immobility in the FST compared to females. A sex by treatment effect was found in peripheral IL-1β levels, where isolated males had a lower level of IL-1β compared to cohoused females. Post-weaning social isolation also altered microglial density in a brain region-specific manner. Isolated voles had higher microglial density in the NAcc, MeA, and CeA, but lower microglial density in the dorsal BNST. Cohoused male voles also had higher microglial density in the PVN compared to cohoused females. Taken together, these data suggest that post-weaning social housing environments can alter peripheral and central immune systems in prairie voles, highlighting a potential role for the immune system in shaping isolation-induced alterations to the brain and behavior.

Highlights

  • Adolescence is a critical time window of development, where one’s environment can have longlasting impacts on health outcomes

  • Isolated voles showed higher microglial densities in the Nucleus Accumbens (NAcc), Medial Amygdala (MeA), Central Amygdala (CeA), but a lower microglial density in the dorsal Bed Nucleus of the Stria Terminalis (BNST) compared to cohoused voles

  • These results suggest that chronic social isolation during a juvenile window may have distinctive effects on both peripheral and central immune function between male and female prairie voles

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Summary

Introduction

Adolescence is a critical time window of development, where one’s environment can have longlasting impacts on health outcomes. During this adolescent window, humans rely on a wide variety of social relationships to develop skills necessary for becoming successful adults. Studies in humans have found that increased social isolation and perceived loneliness are associated with elevated inflammation (Eisenberger et al, 2017; Leschak and Eisenberger, 2019). These long-term changes to physiological systems can have severe impacts on health and mortality. The specific underlying mechanisms of how isolation during adolescence can lead to detrimental behaviors and immune dysregulation remains largely unknown

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