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鸟氨酸脱羧酶和多胺在神经系统发育中的作用:综述

Role of ornithine decarboxylase and the polyamines in nervous system development: a review.

作者信息

Slotkin T A, Bartolome J

出版信息

Brain Res Bull. 1986 Sep;17(3):307-20. doi: 10.1016/0361-9230(86)90236-4.

Abstract

Development of nervous tissue is controlled, in part, by the ornithine decarboxylase (ODC)/polyamine system. Each brain region possesses a unique ontogenetic pattern for ODC, with highest levels of the enzyme associated with periods of most rapid growth. For this reason, perturbation of the ODC profile has proven useful in examinations of teratologic mechanisms and detection of adverse environmental effects during development. More recently, the replication of neuronal cells in developing brain has been shown to require the maintenance of polyamine levels and consequently, depletion of polyamines by alpha-difluoromethylornithine (DFMO, an ODC inhibitor) arrests brain cell maturation. DFMO also interferes with neuronal migration, axonogenesis and synaptogenesis, leading to disruption of the cytoarchitectural organization of brain structures: these results imply a similarly important role for polyamines in post-replicative events. Indeed, [3H]DFMO-autoradiographic localization of ODC in developing cerebellar lamina indicates high levels of activity associated with neuropil, areas of axonal outgrowth, and post-mitotic granule cells. Axonal outgrowth during regeneration after nerve damage in the mature nervous system may display some of the same characteristics as in developing neurons, suggesting that the two processes share common polyamine-dependent mechanisms.

摘要

神经组织的发育部分受鸟氨酸脱羧酶(ODC)/多胺系统的控制。每个脑区都有独特的ODC个体发育模式,该酶的最高水平与生长最快的时期相关。因此,ODC谱的扰动已被证明在发育过程中的致畸机制研究和不良环境影响检测中很有用。最近,已表明发育中的大脑中神经元细胞的复制需要维持多胺水平,因此,α-二氟甲基鸟氨酸(DFMO,一种ODC抑制剂)使多胺耗竭会阻止脑细胞成熟。DFMO还会干扰神经元迁移、轴突形成和突触形成,导致脑结构的细胞结构组织破坏:这些结果表明多胺在复制后事件中也起着同样重要的作用。事实上,[3H]DFMO对发育中小脑板层中ODC的放射自显影定位表明,高水平的活性与神经毡、轴突生长区域和有丝分裂后的颗粒细胞相关。成熟神经系统中神经损伤后再生过程中的轴突生长可能表现出与发育中神经元相同的一些特征,这表明这两个过程共享共同的多胺依赖性机制。

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