4.7 Article

Poly (I:C)-induced maternal immune activation modifies ventral hippocampal regulation of stress reactivity: prevention by environmental enrichment

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 95, Issue -, Pages 203-215

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2021.03.018

Keywords

Inflammation; Fetal programming; Maternal behavior; Maternal care; Glucocorticoid receptor; Corticotropin releasing hormone receptor; Corticotropin releasing factor; Synaptic plasticity; Sex difference; Social approach; Social vigilance; Schizophrenia; Autism; Hippocampus; Prefrontal cortex; Suprammamillary nucleus; Oxytocin; Vasopressin; cFos; CamkIIa; Protein Kinase

Funding

  1. NIMH [R15MH114035]
  2. MCPHS Center for Undergraduate Research Mini-Grants

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The study investigated the effects of maternal immune activation (MIA) on social behavior and HPA axis functioning in mice, and found that enrichment housing could mitigate these effects by improving maternal care. The data suggest that environmental augmentation supports parental care and offspring safety/security, offsetting the effects of early health adversity by buffering HPA axis dysregulation.
Environmental enrichment (EE) has been successfully implemented in human rehabilitation settings. However, the mechanisms underlying its success are not understood. Incorporating components of EE protocols into our animal models allows for the exploration of these mechanisms and their role in mitigation. Using a mouse model of maternal immune activation (MIA), the present study explored disruptions in social behavior and associated hypothalamic pituitary adrenal (HPA) axis functioning, and whether a supportive environment could prevent these effects. We show that prenatal immune activation of toll-like receptor 3, by the viral mimetic polyinosinicpolycytidylic acid (poly(I:C)), led to disrupted maternal care in that dams built poorer quality nests, an effect corrected by EE housing. Standard housed male and female MIA mice engaged in higher rates of repetitive rearing and had lower levels of social interaction, alongside sex-specific expression of several ventral hippocampal neural stress markers. Moreover, MIA males had delayed recovery of plasma corticosterone in response to a novel social encounter. Enrichment housing, likely mediated by improved maternal care, protected against these MIA-induced effects. We also evaluated c-Fos immunoreactivity associated with the novel social experience and found MIA to decrease neural activation in the dentate gyrus. Activation in the hypothalamus was blunted in EE housed animals, suggesting that the putative circuits modulating social behaviors may be different between standard and complex housing environments. These data demonstrate that augmentation of the environment supports parental care and offspring safety/security, which can offset effects of early health adversity by buffering HPA axis dysregulation. Our findings provide further evidence for the viability of EE interventions in maternal and pediatric settings.

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