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小脑顶核电刺激对小鼠脑撞击伤后皮质神经再生的促进作用
引用本文:宋雪珠,刘雁,李又福,刘福达,黎春镛,罗高权,武肖娜.小脑顶核电刺激对小鼠脑撞击伤后皮质神经再生的促进作用[J].中国微侵袭神经外科杂志,2012,17(8):370-372.
作者姓名:宋雪珠  刘雁  李又福  刘福达  黎春镛  罗高权  武肖娜
作者单位:1. 528305,佛山市顺德区桂州医院神经内科
2. 510010,广州军区广州总医院神经内科
基金项目:全军十一五面上项目(编号:106126),广州市科技计划项目(编号:122732961131543)
摘    要:目的探讨小脑顶核电刺激(fastigial nucleus stimulation,FNS)对小鼠脑撞击伤(brain impact injury,BII)后皮质神经再生的促进作用。方法将54只昆明小鼠分为假手术组(n=7)、BII组(n=21)、FNS组(n=7)及FNS+BII组(n=19)。假手术组仅行皮肤切开和颅骨分离,但不撞击脑组织。BII组复制小鼠自由落体脑撞击伤,FNS组单纯行FNS。FNS+BII组在FNS后24 h复制小鼠自由落体脑撞击伤。比较BII组和FNS+BII组伤后的临床运动障碍评分。采用实时荧光定量PCR技术,观察各组小鼠脑撞击伤病灶边缘区生长相关蛋白43(GAP-43)mRNA表达的改变。结果 FNS+BII组临床运动障碍评分在颅脑损伤后3、7、14 d较BII组无明显降低(均P>0.05)。实时荧光定量PCR结果显示:FNS+BII组GAP-43 mRNA表达水平在伤后7 d为(2.69±0.86)pg/μg RNA;BII组为(1.55±0.72)pg/μg RNA,明显低于FNS+BII组(P<0.05)。结论 FNS能显著增加撞击伤后GAP-43 mRNA的表达,促进神经纤维再生,但未见神经运动功能的明显改善。

关 键 词:脑撞击伤  小脑顶核电刺激  生长相关蛋白43  神经再生

Promoting effect of cerebellar fastigiai nucleus stimulation on the cortex neural regeneration after impact brain injury in mice
Song Xuezhu , Liu Yan , Li Youfu , Liu Fuda , Li Chunyong , Luo Gaoquan , Wu Xiaona.Promoting effect of cerebellar fastigiai nucleus stimulation on the cortex neural regeneration after impact brain injury in mice[J].Chinese Journal of Minimally Invasive Neurosurgery,2012,17(8):370-372.
Authors:Song Xuezhu  Liu Yan  Li Youfu  Liu Fuda  Li Chunyong  Luo Gaoquan  Wu Xiaona
Institution:1. Department of Neurology, Guizhou Hospital of Shunde district of Foshan, Foshan, Guangdong 528305, China; 2. Department of Neurology, Guangzhou General Hospital of Guangzhou Military Command, Guangzhou, Guangdong 510010, China
Abstract:Objeeive To explore the promotion effect of cerebellar fastigial nucleus stimulation (FNS) on the cortex neural regeneration after brain impact injury (BII) in mice. Methods Fifty-four mice were divided into sham-operated group (n = 7), BII group (n = 21), FNS group (n = 7) and FNS+BII group (n = 19). Skin incision and skull detaching were performed in sham-operated group without BI/Weigh-drop brain impact injury was replicated in BII group. FNS was performed in FNS group. FNS was performed and 24 h later brain impact injury was induced using weigh-drop method in FNS+BII group. The clinical movement disorder score was evaluated in BII group and FNS+BII group after BII. The expression of growth associated protein 43 (GAP-43) mRNA in the marginal zone of BII lesion was detected by real-time PCR in all the groups. Results There was no significant decrease of clinical movement disorder score in FNS+BII group than that in BII group 3, 7, 14 days after BII (all P 〉 0.05). GAP-43 mRNA expression was 2.69±0.86 pg/μg RNA 7 days after BII in FNS+BII group, which was significantly higher than 1.55±0.72 pg/μg RNA in BII group (P 〈 0.05). Conclusions FNS can significantly increase the expression of GAP-43 mRNA and promote the regeneration of neural fiber in BII mice without the improvement of neurologic movement function.
Keywords:brain impact injury  fastigial nucleus stimulation  growth associated protein-43  nerve regeneration
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