Effect of adenovirus-mediated brain-derived neurotrophic factor on differentiation of endogenetic nerve stem cells from rats after intracerebral hemorrhage
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Effect of adenovirus-mediated brain-derived neurotrophic factor on differentiation of endogenetic nerve stem cells from rats after intracerebral hemorrhage
Journal of Army Medical UniversityVol. 32, Issue 15, Pages: 1628-1631(2010)
Yu Zhen,Chen LiFeng,Tang Ling,Hu Changlin.Effect of adenovirus-mediated brain-derived neurotrophic factor on differentiation of endogenetic nerve stem cells from rats after intracerebral hemorrhage[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(15):1628-1631.
Yu Zhen,Chen LiFeng,Tang Ling,Hu Changlin.Effect of adenovirus-mediated brain-derived neurotrophic factor on differentiation of endogenetic nerve stem cells from rats after intracerebral hemorrhage[J].J Amry Med Univ (J Third Mil Med Univ),2010,32(15):1628-1631.DOI:
Effect of adenovirus-mediated brain-derived neurotrophic factor on differentiation of endogenetic nerve stem cells from rats after intracerebral hemorrhage
于1、3、7、14、2l、28 d进行神经缺失功能评分。免疫荧光单标法观察3组血肿周围GAP-43的表达。免疫荧光双标法观察脑出血大鼠28 d时NSCs的分化。 结果 Ad-BDNF组在第7、14、21、28 天神经缺失功能评分优于NS组和Ad组 (P0.01)。GAP-43在脑出血出血同侧3 d 时表达明显增加,7 d 达高峰,以后逐渐减少。Ad-BDNF组在第3、7、14、21、28天的GAP-43表达明显增加,与NS、Ad组比较差异有统计学意义(P0.05)。28 d时Ad-BDNF组BrdU/NeuN双标阳性细胞率为(39.69±17.45)%、BrdU/GFAP双标阳性细胞率为(63.53±21.68)%,与NS组、Ad组比较明显增加(P0.05)。 结论 腺病毒介导的BDNF可促进脑出血后内源性NSCs的分化和轴突再生,有利于神经功能的恢复。
Abstract
Objective To observe the effects of adenovirus-mediated brain-derived neurotrophic factor (Ad-BDNF) on differentiation of endogenetic nerve stem cells (NSCs) after intracerebral hemorrhage (ICH). Methods A rat ICH model was established by right intrastriatal administration of autologous whole blood. One hundred and twenty-six rats were divided into normal saline (NS) group
adenovirus interference group (Ad group) and Ad-BDNF interference group
42 rats in each group. NS
Ad and Ad-BDNF were injected into the perihematomal area of rats
respectively. Expression of GAP-43 and differentiation of NSCs were observed with single immunofluorescence labeling method and double immunofluorescence labeling method
respectively in 4 weeks after establishment of ICH model. Results The score of NSC function was higher in Ad-BDNF interference group than in NS and Ad interference groups in 7
14
21 and 28 d after establishment of ICH model (P0.01) with no significant difference between NS and Ad interference group(P0.05). The expression level of GAP-43 was significantly higher in the perihematomal area of rats in 3 d after establishment of ICH model
reached its peak in 7 d after establishment of ICH model
and then gradually decreased
but no significant difference was found between NS and Ad interference groups (P0.05). The expression level of GAP-43 was significantly higher in Ad-BDNF interference group than in NS group and Ad interference group in 3
7
14
21 and 28 d after establishment of ICH model (P0.05)
but no significant difference was observed between NS and Ad interference groups (P0.05). The differentiation rates of endogenetic NSCs [BrdU/NeuN=(39.69±17.45)% and BrdU/GFAP=(63.53±21.68)%] were significantly higher in Ad-BDNF interference group than in NS and Ad interference groups in 28 d after establishment of ICH model (P0.05). Conclusion Ad-BDNF can increase the differentiation of endogenetic NSC and improve the recovery of nerve function after ICH.
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