4.2 Article

Hidden talents: Poly (I:C)-induced maternal immune activation improves mouse visual discrimination performance and reversal learning in a sex-dependent manner

Journal

GENES BRAIN AND BEHAVIOR
Volume 20, Issue 7, Pages -

Publisher

WILEY
DOI: 10.1111/gbb.12755

Keywords

acetylcholine; cognitive flexibility; companion loss; compensatory mechanisms; fetal programming; hippocampus; parvalbumin; perineuronal nets; prefrontal cortex; prenatal immune activation; sex differences; social isolation; two-hit

Funding

  1. MCPHS Summer Undergraduate Research Fellowship
  2. MCPHS Center for Undergraduate Research
  3. National Institute of Mental Health [R15MH114035]

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The study found that maternal immune activation had positive effects on visual abilities in male mice and on reversal learning abilities in female mice, but exposure to a "two-hit" stress model led to decreased behavioral learning abilities and changes in gene expression.
While there is a strong focus on the negative consequences of maternal immune activation (MIA) on developing brains, very little attention is directed towards potential advantages of early life challenges. In this study, we utilized a polyinosine-polycytidylic acid (poly(I:C)) MIA model to test visual paired discrimination (PD) and reversal learning (RL) in mice using touchscreen technology. Significant sex differences emerged in that MIA reduced the latency for males to make a correct choice in the PD task while females reached criterion sooner, made fewer errors, and utilized fewer correction trials in RL compared to saline controls. These surprising improvements were accompanied by the sex-specific upregulation of several genes critical to cognitive functioning, indicative of compensatory plasticity in response to MIA. In contrast, when exposed to a 'two-hit' stress model (MIA + loss of the social component of environmental enrichment [EE]), mice did not display anhedonia but required an increased number of PD and RL correction trials. These animals also had significant reductions of CamK2a mRNA in the prefrontal cortex. Appropriate functioning of synaptic plasticity, via mediators such as this protein kinase and others, are critical for behavioral flexibility. Although EE has been implicated in, delaying the appearance of symptoms associated with certain brain disorders, these findings are in line with evidence that it also makes individuals more vulnerable to its loss. Overall, with the right 'dose', early life stress exposure can confer at least some functional advantages, which are lost when the number or magnitude of these exposures become too great.

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