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Repeated allergic asthma in early versus late pregnancy differentially impacts offspring brain and behavior
Jamie S Church1, Juan M Tamayo2, Paul Ashwood2
1Program in Neuroscience and Behavior, Department of Psychology and Education, Mount Holyoke College, 50 College Street, South Hadley, MA 01075, USA.
Insights
Prenatal exposure to allergic asthma during early pregnancy in mice led to anxiety-like behaviors in male offspring. The timing of maternal inflammation significantly impacts offspring development and sex-specific outcomes.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Prenatal stress and inflammation significantly affect offspring development.
- Asthma, a common pregnancy complication, is a major source of prenatal stress and inflammation.
Purpose of the Study:
- To investigate the developmental effects of allergic asthma-induced inflammation during pregnancy on offspring behavior and brain inflammation.
- To determine if the timing of prenatal inflammatory exposure influences these outcomes.
Main Methods:
- Pregnant mice were exposed to ovalbumin (OVA) or a control (PBS) via aerosol during early (gestational days 2-9) or late (gestational days 10-17) pregnancy.
- Maternal serum was analyzed for stress hormones and immune markers.
- Offspring behavior (locomotor, social, anxiety-like, marble burying) was assessed, and brain cytokine levels were measured.
Main Results:
- Early OVA exposure in males resulted in increased anxiety-like behaviors and altered hypothalamic cytokine levels (decreased G-CSF, IL-4, IL-7, IFNγ, TNFα).
- Late gestation exposure increased maternal corticosterone but did not cause sex-specific behavioral deficits in offspring.
- Female offspring did not exhibit behavioral changes, but early OVA exposure reduced specific hypothalamic cytokines in females.
Conclusions:
- The timing of maternal allergic asthma during pregnancy is critical for sex-specific neurodevelopmental outcomes in offspring.
- Maternal immune and stress responses interact to shape fetal programming, with early gestation exposure having lasting behavioral impacts on males.
Background:
Stress during pregnancy and maternal inflammation are two common prenatal factors that impact offspring development. Asthma is the leading chronic condition complicating pregnancy and a common source of prenatal stress and inflammation.
Objective:
The goal of this study was to characterize the developmental impact of repeated allergic asthma inflammation during pregnancy on offspring behavioral outcomes and brain inflammation.
Methods:
Pregnant female C57BL/6 mice were sensitized with ovalbumin (OVA) or PBS vehicle control and then randomly assigned to receive daily aerosol exposures to the same OVA or PBS treatment during early, gestational days (GD) 2-GD9, or late pregnancy, GD10-GD17. Maternal sera were collected after the first and last aerosol induction regimen and measured for concentrations of corticosterone, anti-OVA IgE, and cytokine profiles. Juvenile male and female offspring were assessed for locomotor and social behaviors and later as adults assessed for anxiety-like, and marble burying behaviors using a series of behavioral tasks. Offspring brains were evaluated for region-specific differences in cytokine concentrations.
Results:
In early gestation, both PBS and OVA-exposed dams had similar serum corticosterone concentration at the start (GD2) and end (GD9) of daily aerosol inductions. Only OVA-exposed dams showed elevations in cytokines that imply a diverse and robust T helper cell-mediated immune response. Male offspring of early OVA-exposed dams showed decreases in open-arm exploration in the elevated plus maze and increased marble burying without concomitant changes in locomotor activity or social interactions. These behavioral deficits in early OVA-exposed male offspring were associated with lower concentrations of G-CSF, IL-4, IL-7, IFNγ, and TNFα in the hypothalamus. In late gestation, both PBS and OVA-exposed dams had increased corticosterone levels at the end of daily aerosol inductions (GD17) compared to at the start of inductions (GD10). Male offspring from both PBS and OVA-exposed dams in late gestation showed similar decreases in open arm exploration on the elevated plus maze compared to OVA male offspring exposed in early gestation. No behavioral differences were present in female offspring across all treatment groups. However, females of dams exposed to OVA during early gestation displayed similar reductions as males in hypothalamic G-CSF, IL-7, IL-4, and IFNγ.
Discussion:
The inflammatory responses from maternal allergic asthma in early gestation and resulting increases in anxiety-like behavior in males support a link between the timing of prenatal insults and sex-specific developmental outcomes. Moreover, the heightened stress responses in late gestation and concomitant dampened inflammatory response to allergic asthma suggest that interactions between the maternal immune and stress-response systems shape early life fetal programming.
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