Maternal choline supplementation modulates cognition and induces anti-inflammatory signaling in the prefrontal cortices of adolescent rats exposed to maternal immune activation
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引用次数: 0
Abstract
Maternal infection has long been described as a risk factor for neurodevelopmental disorders, especially autism spectrum disorders (ASD) and schizophrenia. Although many pathogens do not cross the placenta and infect the developing fetus directly, the maternal immune response to them is sufficient to alter fetal neurodevelopment, a phenomenon termed maternal immune activation (MIA). Low maternal choline is also a risk factor for neurodevelopmental disorders, and most pregnant people do not receive enough of it. In addition to its role in neurodevelopment, choline is capable of inducing anti-inflammatory signaling through a nicotinic pathway. Therefore, it was hypothesized that maternal choline supplementation would blunt the neurodevelopmental impact of MIA in offspring through long-term instigation of cholinergic anti-inflammatory signaling.
To model MIA in rats, the viral mimetic polyinosinic:polycytidylic acid (poly(I:C)) was used to elicit a maternal antiviral innate immune response in dams both with and without choline supplementation. Offspring were reared to both early and late adolescent stages (postnatal days 28 and 50, respectively), where anxiety-related behaviors and cognition were examined. After behavioral testing, animals were euthanized, and their prefrontal cortices (PFCs) were collected for analysis. MIA offspring demonstrated sex-specific patterns of altered cognition and repetitive behaviors, which were modulated by maternal choline supplementation. Choline supplementation also bolstered anti-inflammatory signaling in the PFCs of MIA animals at both early and late adolescent stages. These findings suggest that maternal choline supplementation may be sufficient to blunt some of the behavioral and neurobiological impacts of inflammatory exposures in utero, indicating that it may be a cheap, safe, and effective intervention for neurodevelopmental disorders.
长期以来,母体感染一直被描述为神经发育障碍的风险因素,尤其是自闭症谱系障碍(ASD)和精神分裂症。虽然许多病原体不会穿过胎盘直接感染发育中的胎儿,但母体对这些病原体的免疫反应足以改变胎儿的神经发育,这种现象被称为母体免疫激活(MIA)。母体胆碱不足也是神经发育障碍的一个风险因素,大多数孕妇都没有摄入足够的胆碱。除了在神经发育中的作用外,胆碱还能通过烟碱途径诱导抗炎信号传导。为了在大鼠中建立 MIA 模型,研究人员使用病毒模拟物聚肌苷酸:聚胞苷酸(poly(I:C))在补充和不补充胆碱的母体中引起母体抗病毒先天性免疫反应。将后代饲养到青春期早期和晚期(分别为出生后第 28 天和第 50 天),对其焦虑相关行为和认知能力进行检测。行为测试结束后,动物被安乐死,并收集其前额叶皮质(PFC)进行分析。MIA后代表现出了认知和重复行为改变的性别特异性模式,而母体胆碱补充剂可调节这些改变。在青春期早期和晚期阶段,补充胆碱还能增强 MIA 动物前额叶的抗炎信号转导。这些研究结果表明,补充母体胆碱可能足以减弱子宫内炎症暴露对行为和神经生物学的影响,这表明补充胆碱可能是一种廉价、安全且有效的神经发育障碍干预措施。