4.5 Article

Mice Born to Mothers with Gravida Traumatic Brain Injury Have Distorted Brain Circuitry and Altered Immune Responses

期刊

JOURNAL OF NEUROTRAUMA
卷 38, 期 20, 页码 2862-2880

出版社

MARY ANN LIEBERT, INC
DOI: 10.1089/neu.2021.0048

关键词

circuit connectivity; fetal development; gestational injury; immune response; intimate partner violence; maternal brain injury

资金

  1. Phoenix Children's Hospital
  2. Arizona Alzheimer's Consortium
  3. NIH [T32-AG044402]
  4. Fraternal Order of Eagles

向作者/读者索取更多资源

The study suggests that offspring born to pregnant dams who experienced traumatic brain injury (TBI) exhibited significant effects on health, physiology, and behavior, particularly in male offspring. Specific outcomes included lower weight, weakened brain connectivity, and increased anxiety-like behaviors in the male TBI offspring compared to controls. Further research is needed to fully understand the impact of maternal gTBI on offspring development.
Intimate partner violence (IPV) increases risk of traumatic brain injury (TBI). Physical assaults increase in frequency and intensity during pregnancy. The consequences of TBI during pregnancy (gravida TBI; gTBI) on offspring development is unknown, for which stress and inflammation during pregnancy worsen fetal developmental outcomes. We hypothesized that gTBI would lead to increased anxiety- and depression-related behavior, altered inflammatory responses and gut pathology, and distorted brain circuitry in mixed-sex offspring compared to mice born to control mothers. Pregnant dams received either diffuse TBI or sham injury (control) 12 days post-coitum. We found that male gTBI offspring were principal drivers of the gTBI effects on health, physiology, and behavior. For example, male, but not female, gTBI offspring weighed significantly less at weaning compared to male control offspring. At post-natal day (PND) 28, gTBI offspring had significantly weaker intralaminar connectivity onto layer 5 pre-frontal pyramidal neurons compared to control offspring. Neurological performance on anxiety-like behaviors was decreased, with only marginal differences in depressive-like behaviors, for gTBI offspring compared to control offspring. At PND42 and PND58, circulating neutrophil and monocyte populations were significantly smaller in gTBI male offspring than control male offspring. In response to a subsequent inflammatory challenge at PND75, gTBI offspring had significantly smaller circulating neutrophil populations than control offspring. Anxiety-like behaviors persisted during the immune challenge in gTBI offspring. However, spleen immune response and gut histology showed no significant differences between groups. The results compel further studies to determine the full extent of gTBI on fetal and maternal outcomes.

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