Journal
BRAIN BEHAVIOR AND IMMUNITY
Volume 38, Issue -, Pages 142-150Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2014.01.014
Keywords
Intrauterine inflammation; Preterm birth; Mouse model; Lipopolysaccharide; Brain damage; MRI; Behavior
Categories
Funding
- Aramco Services Company Fellowship Fund
- NICHD [K08HD073315]
- NINDS [NS28208]
- NIH [RO1 EB003543]
- Brain Science Institute, Johns Hopkins
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Preterm infants, especially those that are exposed to prenatal intrauterine infection or inflammation, are at a major risk for adverse neurological outcomes, including cognitive, motor and behavioral disabilities. We have previously shown in a mouse model that there is an acute fetal brain insult associated with intrauterine inflammation. The objectives of this study were: (1) to elucidate long-term (into adolescence and adulthood) neurological outcomes by assessing neurobehavioral development, MRI, immunohistochemistry and flow cytometry of cells of immune origin and (2) to determine whether there are any sex-specific differences in brain development associated with intrauterine inflammation. Our results have shown that prenatal exposure appeared to lead to changes in MRI and behavior patterns throughout the neonatal period and during adulthood. Furthermore, we observed chronic brain inflammation in the offspring, with persistence of microglial activation and increased numbers of macrophages in the brain, ultimately resulting in neuronal loss. Moreover, our study highlights the sex-specific differences in long-term sequelae. This study, while extending the growing literature of adverse neurologic outcomes following exposure to inflammation during early development, presents novel findings in the context of intrauterine inflammation. (C) 2014 Elsevier Inc. All rights reserved.
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