Department of Physiology, University of Auckland, Auckland 1023, New Zealand.
The Ritchie Centre, Hudson Institute of Medical Research, Melbourne, Victoria 3168, Australia.
Int J Mol Sci. 2020 Nov 24;21(23):8891. doi: 10.3390/ijms21238891.
Progressive fetal infection/inflammation is strongly associated with neural injury after preterm birth. We aimed to test the hypotheses that progressively developing fetal inflammation leads to neuroinflammation and impaired white matter development and that the histopathological changes can be detected using high-field diffusion tensor magnetic resonance imaging (MRI). Chronically instrumented preterm fetal sheep at 0.7 of gestation were randomly assigned to receive intravenous saline (control; = 6) or a progressive infusion of lipopolysaccharide (LPS, 200 ng intravenous over 24 h then doubled every 24 h for 5 days to induce fetal inflammation, = 7). Sheep were killed 10 days after starting the infusions, for histology and high-field diffusion tensor MRI. Progressive LPS infusion was associated with increased circulating interleukin (IL)-6 concentrations and moderate increases in carotid artery perfusion and the frequency of electroencephalogram (EEG) activity ( < 0.05 vs. control). In the periventricular white matter, fractional anisotropy (FA) was increased, and orientation dispersion index (ODI) was reduced ( < 0.05 vs. control for both). Histologically, in the same brain region, LPS infusion increased microglial activation and astrocyte numbers and reduced the total number of oligodendrocytes with no change in myelination or numbers of immature/mature oligodendrocytes. Numbers of astrocytes in the periventricular white matter were correlated with increased FA and reduced ODI signal intensities. Astrocyte coherence was associated with increased FA. Moderate astrogliosis, but not loss of total oligodendrocytes, after progressive fetal inflammation can be detected with high-field diffusion tensor MRI.
进行性胎儿感染/炎症与早产后脑神经损伤密切相关。我们旨在检验以下假设:逐渐发展的胎儿炎症会导致神经炎症和白质发育受损,并且可以使用高场弥散张量磁共振成像(MRI)检测到组织病理学变化。在妊娠 0.7 时对慢性植入的早产胎儿羊进行随机分组,分别接受静脉注射生理盐水(对照组,n=6)或连续静脉输注脂多糖(LPS,200ng 静脉输注 24 小时,然后每 24 小时加倍,持续 5 天以诱导胎儿炎症,n=7)。在开始输注后 10 天处死绵羊,进行组织学和高场弥散张量 MRI 检查。连续 LPS 输注与循环白细胞介素(IL)-6 浓度增加、颈动脉灌注和脑电图(EEG)活动频率中度增加有关(均<0.05 与对照组相比)。在脑室周围白质中,各向异性分数(FA)增加,取向弥散指数(ODI)降低(均<0.05 与对照组相比)。组织学上,在同一脑区,LPS 输注增加了小胶质细胞激活和星形胶质细胞数量,并减少了总少突胶质细胞数量,但髓鞘形成或未成熟/成熟少突胶质细胞数量无变化。脑室周围白质中星形胶质细胞数量与 FA 增加和 ODI 信号强度降低呈正相关。星形胶质细胞的相干性与 FA 增加相关。在进行性胎儿炎症后,高场弥散张量 MRI 可检测到中度的星形胶质细胞增生,但不会导致总少突胶质细胞丢失。