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bioRxiv · 10.1101/689927

Transient uterine hypercontractility causes oxidative stress in the fetal brain, sex-dependent mitochondrial abnormalities, and altered social behavior of adolescent male rat offspring

Palanisamy, A.·Giri, T.·Jiang, J.·Bice, A.·Quirk, J.·Maloney, S.·Bauer, A.·Garbow, J.·Wozniak, D.
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Abstract

The impact of transient ischemic-hypoxemic insults on the developing fetal brain is poorly understood despite evidence suggesting an association with neurodevelopmental disorders such as schizophrenia and autism. To address this, we designed an aberrant uterine hypercontractility paradigm with oxytocin to better assess the consequences of acute, but transient, placental ischemia-hypoxemia in term pregnant rats. Using MRI imaging, we confirmed that oxytocin-induced aberrant uterine hypercontractility significantly compromised uteroplacental perfusion. This was supported by the observation of oxidative stress and increased lactate concentration in the fetal brain. Genes related to oxidative stress pathways were significantly upregulated in male, but not female, offspring 1 h after oxytocin-induced placental ischemia-hypoxemia. Persistent upregulation of select mitochondrial electron transport chain complex proteins in the anterior cingulate cortex of adolescent male offspring suggested that this sex-specific effect was enduring. Functionally, offspring exposed to oxytocin-induced uterine hypercontractility showed male-specific abnormalities in social behavior with associated region-specific changes in gene expression and functional cortical connectivity. Our findings, therefore, indicate that even transient but severe placental ischemia-hypoxemia could be detrimental to the developing brain and point to a possible mitochondrial link between intrauterine asphyxia and neurodevelopmental disorders.

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Palanisamy, A., Giri, T., Jiang, J., Bice, A., Quirk, J., Maloney, S., Bauer, A., Garbow, J., Wozniak, D.. 2019-07-02. Transient uterine hypercontractility causes oxidative stress in the fetal brain, sex-dependent mitochondrial abnormalities, and altered social behavior of adolescent male rat offspring. https://doi.org/10.1101/689927

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