Department of Pediatrics, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan.
Department of Neural Regenerative Medicine, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo, 060-8556, Japan.
Pediatr Res. 2023 Dec;94(6):1921-1928. doi: 10.1038/s41390-023-02717-9. Epub 2023 Jul 8.
Perinatal brain injury is multifactorial and primarily associated with brain prematurity, inflammation, and hypoxia-ischemia. Although recent advances in perinatal medicine have improved the survival rates of preterm infants, neurodevelopmental disorders remain a significant complication. We tested whether the intravenous infusion of mesenchymal stem cells (MSCs) had therapeutic efficacy against perinatal brain injury in rats.
Pregnant rats at embryonic day (E) 18 received lipopolysaccharide and the pups were born at E21. On postnatal day (PND) 7, the left common carotid artery of each pup was ligated, and they were exposed to 8% oxygen for 2 h. They were randomized on PND10, and MSCs or vehicle were intravenously infused. We performed behavioral assessments, measured brain volume using MRI, and performed histological analyses on PND49.
Infused MSCs showed functional improvements in our model. In vivo MRI revealed that MSC infusion increased non-ischemic brain volume compared to the vehicle group. Histological analyses showed that cortical thickness, the number of NeuN and GAD67 cells, and synaptophysin density in the non-ischemic hemisphere in the MSC group were greater than the vehicle group, but less than the control group.
Infused MSCs improve sensorimotor and cognitive functions in perinatal brain injury and enhance neuronal growth.
Intravenous infusion of MSCs improved neurological function in rats with perinatal brain injury, including motor, sensorimotor, cognitive, spatial, and learning memory. Infused MSCs increased residual (non-ischemic) tissue volume, number of neuronal cells, GABAergic cells, and cortical synapses in the contralesional (right) hemisphere. Intravenous administration of MSC might be suitable for the treatment of perinatal brain injury.
围产期脑损伤是多因素的,主要与脑早产、炎症和缺氧缺血有关。尽管围产期医学的最新进展提高了早产儿的存活率,但神经发育障碍仍然是一个严重的并发症。我们测试了间充质干细胞(MSCs)静脉输注对大鼠围产期脑损伤是否具有治疗效果。
妊娠第 18 天(E)的大鼠接受脂多糖注射,第 21 天分娩。在出生后第 7 天(PND),每只幼鼠的左颈总动脉结扎,然后暴露于 8%氧气中 2 小时。在 PND10 时进行随机分组,MSCs 或载体静脉输注。我们进行行为评估,使用 MRI 测量脑容量,并在 PND49 进行组织学分析。
输注的 MSCs 在我们的模型中显示出功能改善。体内 MRI 显示,与载体组相比,MSC 输注增加了非缺血性脑容量。组织学分析显示,MSC 组非缺血半球的皮质厚度、NeuN 和 GAD67 细胞数量以及突触素密度均大于载体组,但小于对照组。
输注的 MSCs 可改善围产期脑损伤大鼠的感觉运动和认知功能,并促进神经元生长。
MSC 静脉输注改善了围产期脑损伤大鼠的神经功能,包括运动、感觉运动、认知、空间和学习记忆。输注的 MSCs 增加了对侧(右侧)半球残留(非缺血)组织体积、神经元细胞、GABA 能细胞和皮质突触的数量。MSC 的静脉给药可能适合治疗围产期脑损伤。