新生大鼠缺氧缺血脑白质损伤模型学习记忆能力的变化

林凌 张更 林巧梅 林清

解剖学报 ›› 2016, Vol. 47 ›› Issue (6) : 738-743.

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解剖学报 ›› 2016, Vol. 47 ›› Issue (6) : 738-743. DOI: 10.16098/j.issn.0529-1356.2016.06.003
神经生物学

新生大鼠缺氧缺血脑白质损伤模型学习记忆能力的变化

  • 林凌 张更 林巧梅 林清*
作者信息 +

Change of learning and memory ability in neonatal rats with hypoxic-ischemic white matter injury

  • LIN Ling ZHANG Geng LIN Qiao-mei LIN Qing*
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文章历史 +

摘要

目的 通过缺氧、缺血法建立新生大鼠脑白质损伤(WMI)模型,评价大鼠各个生长时期的学习记忆能力及髓鞘碱性蛋白(MBP)表达变化。 方法 新生4日龄SD大鼠100只随机分为对照组和缺氧、缺血WMI组,应用HE染色法观察脑组织病理学改变。于术后4周、8周与12周分别观察大鼠神经行为学和学习记忆能力改变,并应用免疫荧光染色法和Western blotting法观察MBP在大鼠脑内的定位定量表达变化。 结果 HE染色显示,WMI组大鼠出现缺氧、缺血脑白质损伤病理改变。WMI组大鼠神经行为学及学习记忆能力较对照组减弱,差异具有统计学意义(P<0.01)。WMI组各时间点的MBP表达量较对照组降低,差异具有统计学意义(P<0.01)。 结论 新生4日龄SD大鼠发生缺氧、缺血脑白质损伤后,各个生长时期的学习记忆能力均减弱,MBP蛋白表达均减少,推测学习记忆能力减弱可能与MBP蛋白表达减少有关。

Abstract

 Objective To explore changes of the learning and memory ability as well as the myelin basic protein (MBP) expression during various growth periods in neonatal rats with hypoxic-ischemic white matter injury (WMI). Methods New born 4-day-old SD rats were randomly divided into a control group and a hypoxicischemic WMI group. The histology of rat brain tissues was observed by HE staining at 4w after operation. The neurobehavior and the ability of learning and memory were investigated at 4weeks, 8weeks and 12weeks after operation. The distribution and expression of MBP protein were tested by immunofluorescent histochemical staining method and western blotting. Results The hypoxic-ischemic white matter injury was showed by HE staining in WMI group. The weaker ability of neurobehavior and learning and memory were displayed in WMI group compared with the control group (P<0.01). The expression of MBP was significantly decreased in the WMI group compared with the control group(P<0.01). Conclusion The ability of learning and memory was weakened and the expression of MBP protein was decreased in new born 4-day-old SD rats with hypoxic-ischemic white matter injury. The weaker ability of learning and memory may be resulted from the decreased expression of MBP protein.

关键词

脑白质损伤 / 学习 / 记忆 / 髓鞘碱性蛋白 / 免疫荧光 / 免疫印迹法 / 大鼠

Key words

White matter injury / Learning / Memory / Myelin basic protein / Immunofluorescence / Western blotting / Rat

引用本文

导出引用
林凌 张更 林巧梅 林清. 新生大鼠缺氧缺血脑白质损伤模型学习记忆能力的变化[J]. 解剖学报. 2016, 47(6): 738-743 https://doi.org/10.16098/j.issn.0529-1356.2016.06.003
LIN Ling ZHANG Geng LIN Qiao-mei LIN Qing. Change of learning and memory ability in neonatal rats with hypoxic-ischemic white matter injury[J]. Acta Anatomica Sinica. 2016, 47(6): 738-743 https://doi.org/10.16098/j.issn.0529-1356.2016.06.003

参考文献

[1]Hou XL, Fen Q, Tang ZZh,et al. The opinion of expert group on diagnosis, prevention and management in premature infants with white matter injury[J]. Chinese Journal of Neonatology, 2015, 30(3): 175-177.(in Chinese)
侯新琳,冯琪,汤泽中,等.早产儿脑白质损伤诊断、防治与综合管理的专家组意见[J].中国新生儿科杂志,2015, 30(3): 175-177. 
[2]Deng W. Neurobiology of injury to the developing brain[J]. Nat Rev Neurol, 2010, 6(6): 328-336.
[3]Munck P, Haataja L, Maunu J, et al. Cognitive outcome at years of age in finnish infants with very low birth weight born between 2001 and 2006[J]. Acta Paediatr, 2010, 99(3): 359-366.
[4]Petersson KH, Pinar H, Stopa EG, et al. White matter injury after cerebral ischemia in ovine fetuses[J]. Pediatr Res, 2002, 51(6): 768-776.
[5]Liu XB, Shen Y, Plane JM, et al. Vulnerability of premyelinating oligodendrocytes to white-matter damage in neonatal brain injury[J]. Neurosci Bull, 2013, 29 (2): 229-238.
[6]Volpe JJ. Systemic inflammation, oligodendroglial maturation, and the encephalopathy of prematurity[J]. Ann Neurol, 2011, 70(4): 525-529.
[7]Hagen MW, Riddle A, McClendon E, et al. Role of recurrent hypoxia-ischemia in preterm white matter injury severity[J]. PLoS One, 2014, 9(11): el12800.
[8]Back SA, Riddle A, McClure MM. Maturation-dependent vulnerability of perinatal white matter in premature birth[J]. Stroke, 2007, 38(2 Suppl): 724-730.
[9]Back SA, Han BH, Luo NL, et al. Selective vulnerability of late oligodendrocyte progenitors to hypoxia-ischemia[J]. Neurosci, 2002, 22(2): 455-463.
[10]Ikeda T, Mishima K, Yoshikawa T, et al. Selective and long-term learning impairment following neonatal hypoxic-ischemic brain insult in rats[J]. Behav Brain Res, 2001, 118(1): 17-25.
[11]Mishima K, Ikeda T, Aoo N, et al. Hypoxia-ischemic insult in neonatal rats induced slowly progressive brain damage related to memory impairment[J]. Neuroscience Letters, 2005, 376(3): 194-199.
[12]Fields RD.Change in the brain’s white matter[J]. Science, 2010, 330(6005): 768-769.
[13]Back SA, Miller SP. Brain injury in premature neonates: a primary cerebral dysmaturation disorder [J]? Ann Neurol, 2014, 75(4): 469-486.
[14]Buser JR, Maire J, Riddle A, et al. Arrested preoligodendrocyte maturation contributes to myelination failure in premature infants[J]. Ann Neurol, 2012, 71(1): 93-109.
[15]Riddle A, Dean J, Buser JR, et al. Histopathological correlates of magnetic resonance imaging-defined chronic perinatal white matter injury[J]. Ann Neurol, 2011, 70(3): 493-507.

[16]Yamazaki Y, Fujiwara H, Kaneko K, et al. Short and long-term functional plasticity of white Matter induced by oligodendrocyte depolarization in the hippocampus[J]. Glia, 2014, 62(8): 1299-1312.

基金

去铁敏对脑室周围白质软化的治疗作用及机制;脑铁代谢失衡在缺氧缺血脑室周围白质软化中的作用及机制


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