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In Vivo Neurochemical Characterization of Developing Guinea Pigs and the Effect of Chronic Fetal Hypoxia

机译:发育中的豚鼠的体内神经化学特征和慢性胎儿缺氧的影响

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The guinea pig is a frequently used animal model for human pregnancy complications, such as oxygen deprivation or hypoxia, which result in altered brain development. To investigate the impact of in utero chronic hypoxia on brain development, pregnant guinea pigs underwent either normoxic or hypoxic conditions at about 70 % of 65-day term gestation. After delivery, neurochemical profiles consisting of 19 metabolites and macromolecules were obtained from the neonatal cortex, hippocampus, and striatum from birth to 12 weeks postpartum using in vivo H-1 MR spectroscopy at 9.4 T. The effects of chronic fetal hypoxia on the neurochemical profiles were particularly significant at birth. However, the overall developmental trends of neurochemical concentration changes were similar between normoxic and hypoxic animals. Alterations of neurochemicals including N-acetylaspartate (NAA), phosphorylethanolamine, creatine, phosphocreatine, and myo-inositol indicate neuronal loss, delayed myelination, and altered brain energetics due to chronic fetal hypoxia. These observed neurochemical alterations in the developing brain may provide insights into hypoxia-induced brain pathology, neurodevelopmental compromise, and potential neuroprotective measures.
机译:豚鼠是人类怀孕并发症(例如缺氧或缺氧)的常用动物模型,这些并发症会导致大脑发育改变。为了研究子宫内慢性缺氧对大脑发育的影响,怀孕的豚鼠在65天足月妊娠时约有70%经历了常氧或低氧状态。分娩后,使用出生时至产后12周的新生儿皮质,海马和纹状体,在9.4 T处进行体内H-1 MR光谱分析,获得了由19种代谢物和大分子组成的神经化学特征。在出生时尤为重要。然而,常氧和低氧动物的神经化学浓度变化的总体发展趋势相似。包括N-乙酰天门冬氨酸(NAA),磷酰乙醇胺,肌酸,磷酸肌酸和肌醇在内的神经化学物质的变化表明,由于慢性胎儿缺氧,神经元丢失,髓鞘延迟和脑能量改变。这些在发育中的大脑中观察到的神经化学变化可能为缺氧诱导的大脑病理,神经发育受损和潜在的神经保护措施提供了见识。

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