首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Motor deficits are triggered by reperfusion-reoxygenation injury as diagnosed by MRI and by a mechanism involving oxidants
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Motor deficits are triggered by reperfusion-reoxygenation injury as diagnosed by MRI and by a mechanism involving oxidants

机译:运动障碍是由MRI诊断的再灌注-再充氧损伤和涉及氧化剂的机制引起的

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The early antecedents of cerebral palsy (CP) are unknown but are suspected to be due to hypoxia-ischemia (H-I). In our rabbit model of CP, the MRI biomarker, apparent diffusion coefficient (ADC) on diffusion-weighted imaging, predicted which fetuses will develop postnatal hypertonia. Surviving H-I fetuses experience reperfusion-reoxygenation but a subpopulation manifested a continued decline of ADC during early reperfusion-reoxygenation, which possibly represented greater brain injury (RepReOx). We hypothesized that oxidative stress in reperfusion-reoxygenation is a critical trigger for postnatal hypertonia. We investigated whether RepReOx predicted postnatal neurobehavior, indicated oxidative stress, and whether targeting antioxidants at RepReOx ameliorated motor deficits, which included testing of a new superoxide dismutase mimic (MnTnHex-2-PyP). Rabbit dams, 79% gestation (E25), were subjected to 40 min uterine ischemia. Fetal brain ADC was followed during H-I, immediate reperfusion-reoxygenation, and 4-72 h after H-I. Endpoints were postnatal neurological outcome at E32, ADC at end of H-I, ADC nadir during H-I and reperfusion-reoxygenation, and area under ADC curve during the first 20 min of reperfusion-reoxygenation. Antioxidants targeting RepReOx were administered before and/or after uterine ischemia. The new MRI-ADC biomarker for RepReOx improved prediction of postnatal hypertonia. Greater superoxide production, mitochondrial injury, and oligodendroglial loss occurred in fetal brains exhibitingRepReOxthan in those without. The antioxidants, MnTnHex-2-PyP and Ascorbate and Trolox combination, significantly decreased postnatal motor deficits and extent of RepReOx. The etiological link between early injury and later motor deficits can thus be investigated by MRI, and allows us to distinguish between critical oxidative stress that causes motor deficits and noncritical oxidative stress that does not.
机译:脑瘫(CP)的早期先例尚不清楚,但怀疑是由于缺氧缺血(H-1)引起的。在我们的CP兔模型中,MRI生物标记物,弥散加权成像上的表观弥散系数(ADC)预测了哪些胎儿会出生后高渗。存活的H-1胎儿经历了再灌注-再充氧,但亚群显示早期再灌注-再充氧期间ADC持续下降,这可能代表了更大的脑损伤(RepReOx)。我们假设再灌注-再充氧中的氧化应激是产后高渗的关键触发因素。我们调查了RepReOx是否可以预测产后神经行为,是否指示氧化应激以及是否在RepReOx上靶向抗氧化剂可以改善运动功能障碍,包括测试新的超氧化物歧化酶模拟物(MnTnHex-2-PyP)。妊娠率为79%(E25)的兔子大坝经历了40分钟的子宫缺血。在H-1,立即再灌注-再充氧以及H-1后4-72小时内,跟踪胎儿脑ADC。终点是E32的产后神经学预后,H-1结束时的ADC,H-1和再灌注-再充氧期间的ADC最低点以及再灌注-再充氧的前20分钟内ADC曲线下的面积。在子宫缺血之前和/或之后给予靶向RepReOx的抗氧化剂。用于RepReOx的新型MRI-ADC生物标志物改善了产后高渗的预测。表现出RepReOx的胎儿脑部的超氧化物生成,线粒体损伤和少突胶质细胞丢失的发生率高于无此现象的胎儿脑部。抗氧化剂MnTnHex-2-PyP和抗坏血酸与Trolox的组合可显着降低出生后运动功能障碍和RepReOx的程度。因此,可以通过MRI来研究早期损伤与晚期运动功能障碍之间的病因学联系,并使我们能够区分引起运动功能障碍的临界氧化应激和没有引起运动异常的非临界氧化应激。

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