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新生小鼠的轻度间歇性低氧血症会导致永久性神经功能缺陷和白质髓鞘形成不足。

Mild intermittent hypoxemia in neonatal mice causes permanent neurofunctional deficit and white matter hypomyelination.

作者信息

Juliano Courtney, Sosunov Sergey, Niatsetskaya Zoya, Isler Joseph A, Utkina-Sosunova Irina, Jang Isaac, Ratner Veniamin, Ten Vadim

机构信息

Department of Pediatrics, Division of Neonatology, Columbia University, New York, USA.

Department of Pediatrics, Division of Neonatology, Columbia University, New York, USA.

出版信息

Exp Neurol. 2015 Feb;264:33-42. doi: 10.1016/j.expneurol.2014.11.010. Epub 2014 Dec 2.

Abstract

Very low birth weight (VLBW) premature infants experience numerous, often self-limited non-bradycardic episodes of intermittent hypoxemia (IH). We hypothesized that these episodes of IH affect postnatal white matter (WM) development causing hypomyelination and neurological handicap in the absence of cellular degeneration. Based on clinical data from ten VLBW neonates; a severity, daily duration and frequency of non-bradycardic IH episodes were reproduced in neonatal mice. Changes in heart rate and cerebral blood flow during IH were recorded. A short-term and long-term neurofunctional performance, cerebral content of myelin basic protein (MBP), 2'3' cyclic-nucleotide 3-phosphodiesterase (CNPase), electron microscopy of axonal myelination and the extent of cellular degeneration were examined. Neonatal mice exposed to IH exhibited no signs of cellular degeneration, yet demonstrated significantly poorer olfactory discrimination, wire holding, beam and bridge crossing, and walking-initiation tests performance compared to controls. In adulthood, IH-mice demonstrated no alteration in navigational memory. However, sensorimotor performance on rota-rod, wire-holding and beam tests was significantly worse compared to naive littermates. Both short- and long-term neurofunctional deficits were coupled with decreased MBP, CNPase content and poorer axonal myelination compared to controls. In neonatal mice mild, non-ischemic IH stress, mimicking that in VLBW preterm infants, replicates a key phenotype of non-cystic WM injury: permanent hypomyelination and sensorimotor deficits. Because this phenotype has developed in the absence of cellular degeneration, our data suggest that cellular mechanisms of WM injury induced by mild IH differ from that of cystic periventricular leukomalacia where the loss of myelin-producing cells and axons is the major mechanism of injury.

摘要

极低出生体重(VLBW)早产儿会经历无数次通常为自限性的非心动过缓性间歇性低氧血症(IH)发作。我们推测,这些IH发作会影响出生后白质(WM)的发育,在无细胞变性的情况下导致髓鞘形成不足和神经功能障碍。基于10例VLBW新生儿的临床数据,在新生小鼠中重现了非心动过缓性IH发作的严重程度、每日持续时间和发作频率。记录了IH期间心率和脑血流量的变化。检测了短期和长期神经功能表现、髓鞘碱性蛋白(MBP)、2',3'-环核苷酸3'-磷酸二酯酶(CNPase)的脑含量、轴突髓鞘形成的电子显微镜检查以及细胞变性程度。暴露于IH的新生小鼠没有细胞变性的迹象,但与对照组相比,在嗅觉辨别、抓线、横梁和过桥以及行走启动测试中的表现明显较差。成年后,IH小鼠在导航记忆方面没有改变。然而,与同窝幼崽相比,在转棒、抓线和横梁测试中的感觉运动表现明显更差。与对照组相比,短期和长期神经功能缺陷均与MBP、CNPase含量降低以及轴突髓鞘形成较差有关。在新生小鼠中,模拟VLBW早产儿的轻度、非缺血性IH应激,重现了非囊性WM损伤的一个关键表型:永久性髓鞘形成不足和感觉运动缺陷。由于这种表型是在无细胞变性的情况下发展而来的,我们的数据表明,轻度IH诱导的WM损伤的细胞机制与囊性脑室周围白质软化不同,后者髓鞘生成细胞和轴突的丧失是主要损伤机制。

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