4.7 Article

Behavioral Alterations and Decreased Number of Parvalbumin-Positive Interneurons in Wistar Rats after Maternal Immune Activation by Lipopolysaccharide: Sex Matters

Journal

Publisher

MDPI
DOI: 10.3390/ijms22063274

Keywords

lipopolysaccharide; maternal immune activation; prenatal infection; chronic bacterial infection; parvalbumin-positive interneurons; macrocephaly; schizophrenia; autism; sex differences; development

Funding

  1. Czech Science Foundation (GACR) [19-03016S]
  2. Czech Health Research Council (AZV) [17-30833A]
  3. MH CZ-DRO (National Institute of Mental Health-NIMH) [IN: 00023752]
  4. project Sustainability for the National Institute of Mental Health [LO1611]
  5. Ministry of Education, Youth and Sports of the Czech Republic under the NPU I program
  6. [GA UK 172515]
  7. [RVO:67985823]

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Maternal immune activation during pregnancy can lead to social and communication impairments in adult offspring, along with changes in various behaviors, including deficits in prepulse inhibition in females and increased startle reaction in males. Brain changes are evident in both sexes, while the sex of the offspring plays a crucial role in the development of MIA-induced behavioral alterations.
Maternal immune activation (MIA) during pregnancy represents an important environmental factor in the etiology of schizophrenia and autism spectrum disorders (ASD). Our goal was to investigate the impacts of MIA on the brain and behavior of adolescent and adult offspring, as a rat model of these neurodevelopmental disorders. We injected bacterial lipopolysaccharide (LPS, 1 mg/kg) to pregnant Wistar dams from gestational day 7, every other day, up to delivery. Behavior of the offspring was examined in a comprehensive battery of tasks at postnatal days P45 and P90. Several brain parameters were analyzed at P28. The results showed that prenatal immune activation caused social and communication impairments in the adult offspring of both sexes; males were affected already in adolescence. MIA also caused prepulse inhibition deficit in females and increased the startle reaction in males. Anxiety and hypolocomotion were apparent in LPS-affected males and females. In the 28-day-old LPS offspring, we found enlargement of the brain and decreased numbers of parvalbumin-positive interneurons in the frontal cortex in both sexes. To conclude, our data indicate that sex of the offspring plays a crucial role in the development of the MIA-induced behavioral alterations, whereas changes in the brain apparent in young animals are sex-independent.

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