产前酒精暴露和绒毛膜羊膜炎导致微结构脑损伤的临床前研究

Annals of pediatric research Pub Date : 2020-01-01 Epub Date: 2020-02-17
Jessie R Maxwell, Tracylyn R Yellowhair, Suzy Davies, Danny A Rogers, Krystle L McCarson, Daniel D Savage, Lauren L Jantzie
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引用次数: 0

摘要

背景:在美国,产前酒精暴露(PAE)每年影响2%至5%的新生儿。怀孕期间饮酒的妇女患绒毛膜羊膜炎(CHORIO)的几率增加五倍。PAE和CHORIO都会引起包括主要白质束在内的多个大脑区域的微结构损伤。目的:利用先前建立的两种动物模型,我们假设PAE+CHORIO联合治疗比PAE单独治疗会导致更大的髓鞘形成和结构完整性缺陷。材料与方法:妊娠期Long-Evans大鼠自愿饮用5%乙醇或糖精,直至妊娠第19天(GD)。GD19时,1组PAE大鼠分别阻断子宫动脉30 min并在每个羊膜囊内注射脂多糖(LPS)诱导CHORIO。其余的PAE组和糖精对照组进行假手术。幼崽于GD22出生,并于出生后第24天断奶。在PD28时,处死后代,用离体弥散张量成像(DTI)检查其大脑。结果:与对照组相比,单独PAE不影响子代出生体重、死亡率或任何DTI指标。相比之下,PAE+CHORIO显著降低了后代的存活率,并且在存活的幼崽中,增加了内侧额叶皮层的径向扩散率(RD),降低了内侧和腹侧额叶皮层以及荚膜区域的分数各向异性(FA)。结论:中度PAE+CHORIO合并导致死亡率增加,并伴有弥漫性微结构脑损伤,出现在年龄为28岁的青少年后代中。未来的研究应该检查PAE在多大程度上加剧了CHORIO引起的损伤,以及这些缺陷是否会持续到成年期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Prenatal Alcohol Exposure and Chorioamnionitis Results in Microstructural Brain Injury in a Preclinical Investigation.

Prenatal Alcohol Exposure and Chorioamnionitis Results in Microstructural Brain Injury in a Preclinical Investigation.

Prenatal Alcohol Exposure and Chorioamnionitis Results in Microstructural Brain Injury in a Preclinical Investigation.

Prenatal Alcohol Exposure and Chorioamnionitis Results in Microstructural Brain Injury in a Preclinical Investigation.

Background: Prenatal Alcohol Exposure (PAE) impacts 2% to 5% of infants born in the United States yearly. Women who consume alcohol during pregnancy have a five-fold increased rate of Chorioamnionitis (CHORIO). Both PAE and CHORIO cause microstructural injury to multiple brain regions including major white matter tracts.

Objective: Utilizing two previously established animal models, we hypothesized that the combination of PAE+CHORIO would result in greater deficits in myelination and structural integrity than PAE alone.

Material and methods: Pregnant Long-Evans rats voluntarily drank 5% ethanol or saccharin until Gestational Day 19 (GD). On GD19, CHORIO was induced in one group of PAE dams by a 30 min uterine artery occlusion and injection of Lipopolysaccharide (LPS) into each amniotic sac. The remaining PAE dams and saccharin controls underwent sham surgery. Pups were born on GD22 and weaned on Postnatal Day 24 (PD). On PD28, offspring were sacrificed, and their brains examined using ex-vivo Diffusion Tensor Imaging (DTI).

Results: Compared to control, PAE alone did not affect offspring birth weights, mortality or any DTI measures. In contrast, PAE+CHORIO significantly reduced offspring survival and, in surviving pups, increased Radial Diffusivity (RD) in medial frontal cortex and decreased Fractional Anisotropy (FA) in medial and ventral frontal cortex and within capsular regions.

Conclusion: The combination of moderate PAE+CHORIO results in an increased mortality, concomitant with diffuse microstructural brain injury noted in young adolescent offspring at PD28. Future studies should examine the extent to which PAE exacerbates the damage caused by CHORIO alone and whether these deficits persist into adulthood.

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