新生小鼠兴奋毒性脑损伤的神经行为功能研究

齐志业, 贺湘英, 李琪, 莫亚雄, 梁琨

中国当代儿科杂志 ›› 2009, Vol. 11 ›› Issue (03) : 191-193.

PDF(1002 KB)
PDF(1002 KB)
中国当代儿科杂志 ›› 2009, Vol. 11 ›› Issue (03) : 191-193.
新生儿疾病专栏

新生小鼠兴奋毒性脑损伤的神经行为功能研究

  • 齐志业,贺湘英,李琪,莫亚雄,梁琨
作者信息 +

Neurobehavioral function of neonatal mice following excitotoxic brain damage

  • QI Zhi-Ye, HE Xiang-Ying, LI Qi, MO Ya-Xiong, LIANG Kun.
Author information +
文章历史 +

摘要

目的:探讨兴奋毒性脑损伤模型小鼠神经行为功能改变情况,为围生期脑损伤的神经保护研究提供新的实验方法。方法:生后5日ICR种小鼠55只,采用完全随机的方法分为空白组、生理盐水组和鹅膏蕈氨酸(ibotenic acid,IA)组,用IA建立兴奋毒性脑损伤模型,小鼠生后第6,7,8,9,10日进行平面翻正实验、生后第8,10,12日进行游泳实验、生后第33和34日进行Y-迷宫分辨学习实验。结果:IA组小鼠生后第6~10日翻正实验时间为2.12±0.61、1.86±0.65、1.50±0.51、1.28±0.29、1.01±0.15,明显长于空白组和生理盐水组(P<0.05),生后第8~12日游泳实验评分为6.33±0.98、6.87±0.74、7.13±0.64,明显低于空白组和生理盐水组(P<0.05);IA组Y-迷宫分辨学习实验“学会”次数为19.79±2.42,明显多于空白组和生理盐水组的 16.29±2.48,16.30±2.37(P<0.05)、正确反应率86.7%,明显低于空白组和生理盐水组的96.5%,95.0%(P<0.05)。结论:新生小鼠兴奋毒性脑损伤模型发育反射和学习记忆功能都受到损伤,可以用行为学的方法对兴奋毒性脑损伤小鼠早期发育反射和远期行为进行评估。[中国当代儿科杂志,2009,11(3):191-193]

Abstract

OBJECTIVE: To assess the changes of neurobehavioral function in a neonatal mouse model of excitotoxic brain damage. METHODS: Fifty-five 5-day-old ICR neonatal mice were randomly assigned to three groups: blank (no intravenous) control (n=20), saline control (n=20) and excitotoxic brain damage model (ibotenic acid treatment, n=15). Behavioral function was evaluated by the surface righting reflex test (postnatal days 6-10), the swimming test (postnatal days 8-12) and the Y-maze discrimination learning test (postnatal days 33-34). RESULTS: Righting time in the surface righting reflex test in the ibotenic acid treatment group on postnatal days 6-10 was more prolonged than that in the two control groups (P<0.05). Swimming test scores in the ibotenic acid treatment group were significantly lower than those in the two control groups (P<0.05). In the Y-maze discrimination learning test, the mice from the ibotenic acid treatment group performed significantly worse than two control groups, presenting with increased learning times (19.79±2.42 vs 16.29±2.48 or 16.30±2.37; P<0.05) and achieving a lower correct percentage (86.7% vs 96.5% or 95.0%) (P<0.05). CONCLUSIONS:The developmental reflexes and learning and memory functions were impaired in neonatal mice following excitotoxic brain damage. Behavioral testing is useful in the evaluation of early developmental reflexes and long-term neurobehavioral outcome in neonatal mice with excitotoxic brain damage.[Chin J Contemp Pediatr, 2009, 11 (3):191-193]

关键词

鹅膏蕈氨酸 / 兴奋毒性 / 脑损伤 / 行为 / 新生小鼠

Key words

Ibotenic acid / Excitotoxic / Brain damage / Behavior / Neonatal mice

引用本文

导出引用
齐志业, 贺湘英, 李琪, 莫亚雄, 梁琨. 新生小鼠兴奋毒性脑损伤的神经行为功能研究[J]. 中国当代儿科杂志. 2009, 11(03): 191-193
QI Zhi-Ye, HE Xiang-Ying, LI Qi, MO Ya-Xiong, LIANG Kun. Neurobehavioral function of neonatal mice following excitotoxic brain damage[J]. Chinese Journal of Contemporary Pediatrics. 2009, 11(03): 191-193
中图分类号: R-33   

参考文献

[1]Inage YW, Itoh M, Takashima S. Correlation between cerebrovascular maturity and periventricular leukomalacia[J].Pediatr Neurol, 2000, 22 (3):204-208.
[2]毛健.早产儿脑白质损伤的有关问题[J].中国实用儿科杂志, 2002, 17(7):386-389.
[3]Rogido M, Husson I, Bonnier C, Lallemand MC, Mérienne C, Gregory GA,et al. Fructose-1,6-biphosphate prevents excitotoxic neuronal cell death in the neonatal mouse brain[J]. Brain Res Dev Brain Res, 2003, 140(2):287-297.
[4]Marret S, Mukendi R, Gadisseux JF, Gressens P, Evrard P. Effect of ibotenate on brain development: an excitotoxic mouse model of microgyria and posthypoxic-like lesions[J]. Neuropathol Exp Neurol, 1995, 54(3):358-370.
[5]Kihara T, Surjono TW, Sakamoto M, Matsuo T, Yasuda Y, Tanimura T.Effects of prenatal rubratoxin-B exposure on behaviors of mouse offspring[J].Toxicol Sci, 2001, 61(2):368-373.
[6]Xu XH, Zhao TQ. Effects of puerarin on D-galactose-induced memory deficits in mice [J].Acta Pharmacol Sin, 2002, 23(7):587-590.
[7]Roohey T, Raju TN, Moustogiannis AN. Animal models for the study of perinatal hypoxic-ischemic encephalopathy: a critical analysis[J]. Early Hum Dev, 1997, 47 (2):115-146.
[8]Ikeda T, Mishima K, Yoshikawa T, Iwasaki K, Fujiwara M, Xia YX, 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.
[9]周丛乐,姜毅,汤泽中,王素寰,姜凌云.早产儿脑白质损伤的发生、预后与病因探讨[J].中华围产医学杂志, 2003, 6(6):325-328.
[10]王云甫,范华燕,任传成,何国厚,叶天雄,余绍祖.局灶性脑缺血后海马各区NMDAR表达的实验研究[J].临床神经病学杂志, 2001, 14(1):27-29.
[11]Loftis JM, Janowsky A. The N-methyl-D-aspartate receptor subunit NR2B: localization, functional properties, regulation, and clinical implications[J]. Pharmacol Ther, 2003, 97(1):55-85.
[12]Vorhee CV. Behavioral and functional ontogeny: biomarkers of neurotoxicity[M].//Chang LW. Principles of Neurotoxicology. New York:Marcel Dekker, Inc, 1994, 241-250.
[13]钟乐,王霞,余小河,杨于嘉.新生大鼠缺氧缺血性脑损伤后的远期行为学测试[J].中国当代儿科杂志,2005,7(3):245-248.
[14]刘美娜,庄思齐,张红宇,覃肇源,李晓瑜.早期高压氧治疗对氧缺血性脑损伤新生大鼠的远期保护作用[J].中国当代儿科杂志,2006,8(3):216-220.


PDF(1002 KB)

Accesses

Citation

Detail

段落导航
相关文章

/