Department of Ophthalmology, Visual and Anatomical Sciences, Wayne State University School of Medicine, Detroit, Michigan, 48201, USA.
Perinatology Research Branch, Division of Obstetrics and Maternal-Fetal Medicine, Division of Intramural Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, U.S. Department of Health and Human Services (NICHD/NIH/DHHS), Bethesda, Maryland, 20847, and Detroit, Michigan, 48201, USA; Department of Obstetrics and Gynecology, University of Michigan Health System, Ann Arbor, Michigan, 48109, USA; Department of Epidemiology and Biostatistics, College of Human Medicine, Michigan State University, East Lansing, Michigan, 48824, USA; Center for Molecular Medicine and Genetics, Wayne State University, Detroit, Michigan, 48201, USA; Detroit Medical Center, Detroit, Michigan, 48201, USA.
Neuroimage. 2019 Oct 15;200:601-606. doi: 10.1016/j.neuroimage.2019.05.069. Epub 2019 May 31.
To achieve sufficient precision of R1 (=1/T1) maps of the fetal brain in utero to perform QUEnch-assiSTed (QUEST) MRI in which a significant anti-oxidant-induced reduction in R1 indicates oxidative stress.
C57BL/6 mouse fetuses in utero were gently and non-surgically isolated and secured using a homemade 3D printed clip. Using a commercial receive-only surface coil, brain maps of R1, an index sensitive to excessive and continuous free radical production, were collected using either a conventional Cartesian or a non-Cartesian (periodically rotated overlapping parallel lines with enhanced reconstruction) progressive saturation sequence. Data were normalized to the shortest TR time to remove bias. To assess oxidative stress, brain R1 maps were acquired on the lipopolysaccharide (LPS) model of preterm birth ± rosiglitazone (ROSI, which has anti-oxidant properties); phosphate buffered saline (PBS) controls ± ROSI were similarly studied.
Sufficient quality R1 maps were generated by a combination of the 3D printed clip, surface coil detection, non-Cartesian sequence, and normalization scheme ensuring minimal fetal movement, good detection sensitivity, reduced motion artifacts, and minimal baseline variations, respectively. In the LPS group, the combined caudate-putamen and thalamus region R1 was reduced (p < 0.05) with ROSI treatment consistent with brain oxidative stress; no evidence for oxidative stress was found in the pons region. In the PBS control group, brain R1's did not change with ROSI treatment.
The sensitivity and reproducibility of the combined approaches described herein enabled first-time demonstration of regional oxidative stress measurements of the fetal brain in utero using QUEST MRI.
为了实现胎儿脑 R1(=1/T1)图谱在宫内的足够精度,以进行 QUEnch-assiSTed(QUEST)MRI,其中 R1 的显著抗氧化诱导降低表明存在氧化应激。
将 C57BL/6 小鼠胎儿在宫内轻轻且非手术地分离出来,并使用自制的 3D 打印夹固定。使用商业接收线圈,使用传统的笛卡尔或非笛卡尔(周期性旋转重叠平行线增强重建)逐步饱和序列,收集 R1(对过度和持续自由基产生敏感的指标)的脑图谱。数据归一化为最短 TR 时间以消除偏差。为了评估氧化应激,在早产的脂多糖(LPS)模型上获取脑 R1 图谱 ± 罗格列酮(ROSI,具有抗氧化特性);同样研究了磷酸盐缓冲盐水(PBS)对照 ± ROSI。
通过 3D 打印夹、表面线圈检测、非笛卡尔序列和归一化方案的组合,生成了足够质量的 R1 图谱,这些方法分别确保了最小的胎儿运动、良好的检测灵敏度、减少运动伪影和最小的基线变化。在 LPS 组中,联合尾状核和丘脑区域的 R1 降低(p < 0.05),ROSI 治疗一致,与脑氧化应激一致;在脑桥区域未发现氧化应激的证据。在 PBS 对照组中,ROSI 治疗未改变脑 R1。
本文所述的联合方法的敏感性和重现性使首次能够使用 QUEST MRI 对胎儿脑进行区域性氧化应激测量。