Department of Neonatology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Oxid Med Cell Longev. 2022 May 31;2022:5769784. doi: 10.1155/2022/5769784. eCollection 2022.
Preterm birth disrupts cerebellar development, which may be mediated by systemic oxidative stress that damages neuronal developmental stages. Impaired cerebellar neurogenesis affects several downstream targets important for cognition, emotion, and speech. In this study, we demonstrate that oxidative stress induced with high oxygen (80%) for three or five postnatal days (P3/P5) could significantly damage neurogenesis and proliferative capacity of granular cell precursor and Purkinje cells in rat pups. Reversal of cellular neuronal damage after recovery to room air (P15) was augmented by treatment with caffeine. However, downstream transcripts important for migration and differentiation of postmitotic granular cells were irreversibly reduced by hyperoxia, without rescue by caffeine. Protective effects of caffeine in the cerebellum were limited to neuronal survival but failed to restore important transcript signatures.
早产会破坏小脑的发育,这可能是由系统性氧化应激引起的,氧化应激会损害神经元的发育阶段。小脑神经发生受损会影响到几个下游的重要靶点,这些靶点对认知、情感和言语至关重要。在这项研究中,我们证明了用高氧(80%)处理三天或五天的新生鼠(P3/P5)可显著破坏颗粒细胞前体细胞和浦肯野细胞的神经发生和增殖能力。在恢复到常氧(P15)后,用咖啡因处理可增强细胞神经元损伤的逆转。然而,过度的氧气会不可逆地降低对颗粒细胞有丝分裂后迁移和分化很重要的下游转录物,而咖啡因则无法挽救。咖啡因在小脑内的保护作用仅限于神经元存活,但未能恢复重要的转录特征。