Maternal obesity alters fetal neuroinflammation in a murine model of preterm birth

Katherine M. Leonard DO , Stacey S. Schmiedecke MD , Rebecca L. Talley BS , Jennifer R. Damicis BS , Robert B. Walton MD , Irina Burd MD, PhD , Peter G. Napolitano MD , Nicholas Ieronimakis PhD
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Abstract

BACKGROUND

Preterm birth from intrauterine infection is a leading cause of neonatal neurologic morbidity. Likewise, maternal obesity is associated with intra-amniotic infection and inflammation. Whether maternal obesity is a risk factor for fetal brain injury that occurs with premature birth remains unknown. This study hypothesized that maternal obesity intensifies fetal neuroinflammation in the setting of premature delivery.

OBJECTIVE

This study aimed to examine the influence of maternal obesity on perinatal neuroinflammatory responses that arise with preterm birth using a murine model.

STUDY DESIGN

Dams with obesity were generated via a high-fat diet that was maintained throughout pregnancy. In parallel, dams without obesity (normal) received a control diet. All dams were paired with males on normal diet. Pregnant dams were randomized to receive an intrauterine administration of bacterial endotoxin (lipopolysaccharide) or the vehicle (phosphate-buffered saline) on embryo day 15.5 of what is typically a 19- to 21-day gestation. Fetal brains were harvested 6 hours after intrauterine administrations, and the expressions of key inflammatory cytokines (Il1b, Il6, and Tnf) and panels of metabolic, immune, and inflammatory genes were analyzed.

RESULTS

With the phosphate-buffered saline, there was no difference in gene expression related to maternal obesity. There were substantial differences in Il6 and immune/inflammatory expression profiles in fetal brains from dams with obesity vs normal dams that received lipopolysaccharide. Few differences were observed among the metabolic genes examined under these conditions. The gene expression pattern associated with maternal obesity correlated with pathways related to white matter injury.

CONCLUSION

The expression of neuroinflammatory markers instigated by bacterial endotoxin via intrauterine lipopolysaccharide was greater in embryo brains obtained from dams with obesity. Expression profiles suggest that in combination with intrauterine inflammation, maternal obesity may increase the risk of fetal white matter injury. Further investigation is warranted to understand the relationship between maternal health and neurologic outcomes associated with prematurity.

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在早产小鼠模型中,母体肥胖会改变胎儿的神经炎症。
背景宫内感染导致的早产是新生儿神经系统发病的主要原因。同样,产妇肥胖也与羊膜腔内感染和炎症有关。孕产妇肥胖是否是早产导致胎儿脑损伤的风险因素仍是未知数。本研究假设,在早产的情况下,母体肥胖会加剧胎儿的神经炎症。研究设计肥胖的母体是通过在整个孕期维持高脂肪饮食而产生的。与此同时,未患肥胖症的母鼠(正常)接受对照饮食。所有母鼠都与正常饮食的雄鼠配对。怀孕母鼠被随机分配到接受细菌内毒素(脂多糖)或载体(磷酸盐缓冲盐水)的子宫内给药,给药时间为胚胎发育的第15.5天,通常为妊娠期的19-21天。宫内给药 6 小时后采集胎儿大脑,分析关键炎症细胞因子(Il1b、Il6 和 Tnf)以及代谢、免疫和炎症基因的表达。肥胖母体与接受脂多糖的正常母体相比,胎儿大脑中的Il6和免疫/炎症基因表达谱存在很大差异。在这些条件下,几乎没有观察到代谢基因之间的差异。结论 通过宫内脂多糖细菌内毒素引起的神经炎症标记物在肥胖母体胚胎大脑中的表达量更大。表达谱表明,母体肥胖与宫内炎症相结合,可能会增加胎儿白质损伤的风险。要了解孕产妇健康与早产相关神经系统结果之间的关系,还需要进一步的研究。
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来源期刊
AJOG global reports
AJOG global reports Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Perinatology, Pediatrics and Child Health, Urology
CiteScore
1.20
自引率
0.00%
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0
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