Social isolation alters behavior, the gut-immune-brain axis, and neurochemical circuits in male and female prairie voles

• Published in: Neurobiology of stress Vol. 13; p. 100278
• Main Authors: Donovan, Meghan, Mackey, Calvin S., Platt, Grayson N., Rounds, Jacob, Brown, Amber N., Trickey, Darryl J., Liu, Yan, Jones, Kathryn M., Wang, Zuoxin
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.11.2020; Elsevier
• Subjects: Anaeroplasma; Gut microbiome-immune-brain axis; Microglia; Original; Oxytocin; Sex difference; Social isolation; Gut microbiome-immune-brain axis; Anaeroplasma; Oxytocin; Social isolation; Sex difference; Microglia
• ISSN: 2352-2895; 2352-2895
• DOI: 10.1016/j.ynstr.2020.100278

The absence of social support, or social isolation, can be stressful, leading to a suite of physical and psychological health issues. Growing evidence suggests that disruption of the gut-immune-brain axis plays a crucial role in the negative outcomes seen from social isolation stress. However, the mechanisms remain largely unknown. The socially monogamous prairie vole (Microtus ochrogaster) has been validated as a useful model for studying negative effects of social isolation on the brain and behaviors, yet how the gut microbiome and central immune system are altered in isolated prairie voles are still unknown. Here, we utilized this social rodent to examine how social isolation stress alters the gut-immune-brain axis and relevant behaviors. Adult male and female prairie voles (n = 48 per sex) experienced social isolation or were cohoused with a same-sex cagemate (control) for six weeks. Thereafter, their social and anxiety-like behaviors, neuronal circuit activation, neurochemical expression, and microgliosis in key brain regions, as well as gut microbiome alterations from the isolation treatment were examined. Social isolation increased anxiety-like behaviors and impaired social affiliation. Isolation also resulted in sex- and brain region-specific alterations in neuronal activation, neurochemical expression, and microgliosis. Further, social isolation resulted in alterations to the gut microbiome that were correlated with key brain and behavioral measures. Our data suggest that social isolation alters the gut-immune-brain axis in a sex-dependent manner and that gut microbes, central glial cells, and neurochemical systems may play a critical, integrative role in mediating negative outcomes from social isolation. •Social isolation increased anxiety-like behaviors and impaired social affiliation.•Isolation altered neuronal activation and neurochemical expression in the brain.•Isolation stress increased microgliosis in a brain region-specific manner.•Isolation stress also resulted in alterations to the gut microbiome.•Social isolation altered the gut-immune-brain axis in a sex-dependent manner.