南方医科大学学报 ›› 2017, Vol. 37 ›› Issue (04): 551-.

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重组人促红细胞生成素对衰老大鼠脑组织不同部位BDNF表达的影响

王虎清,高震,陈梦燚,吴海琴,张桂莲,展淑琴,卜宁,刘璟洁,翟跃芬   

  • 出版日期:2017-04-20 发布日期:2017-04-20

Effects of recombinant human erythropoietin on brain-derived neurotrophic factor expression in different brain regions of aging rats

  • Online:2017-04-20 Published:2017-04-20

摘要: 目的探讨重组人促红细胞生成素(rhEPO)对衰老大鼠脑组织内不同部位脑源性神经营养因子(BDNF)表达的影响。方 法40只2月龄雄性SD大鼠,随机分为4组:阴性对照组(N),D-半乳糖组(D),EPO干预组(E),阳性对照组(P),每组10只。应 用免疫组化染色对比观察外源性rhEPO干预后D-半乳糖衰老大鼠脑组织不同部位BDNF表达的变化。结果不同组大鼠比较 发现相同部位BDNF表达存在显著差异:D组大鼠海马CA1、CA3、DG及额叶皮质区BDNF阳性细胞计数较N组相同部位明显 减少(P<0.05),而应用rhEPO干预后的E组和P组大鼠海马CA1、CA3、DG及大脑皮质运动区BDNF阳性细胞计数较D组及N 组相同部位显著增加(P<0.05);但E组和P组比较无差异。同组大鼠不同部位BDNF阳性细胞比较发现:同组大鼠不同部位 BDNF阳性细胞个数存在显著不同(P<0.05),其中额叶皮质区阳性细胞数最多,其次是海马CA3区,海马DG区,海马CA1区。 结论rhEPO对增强大鼠神经细胞BDNF的表达具有普遍性,提示rhEPO可能能够通过增强内源性BDNF对神经系统衰老发挥 保护作用。

Abstract: Objective To explore the effect of recombinant human erythropoietin (rhEPO) on expression of brain-derived neurotrophic factor (BDNF) in different brain regions of aging rats. Methods Forty male SD rats were randomized equally into negative control group, D-galactose group, EPO treatment group, and positive control group. Rat models of subacute aging were established by continuous subcutaneous injection of 5% D-galactose. Immunohistochemical staining was used to analyze the variation of BDNF expressions in different brain regions of the aging rats with different treatments. Results Significant brain region-specific differences in BDNF expression were found among the rats in different groups. Compared with those in the negative control group, the numbers of BDNF-positive cells in the hippocampal CA1 region, CA3 region, dentate gyrus (DG) and frontal cortex were all decreased obviously in D-galactose group (P<0.05) but increased in both EPO group and the positive control group (P<0.05) without significant differences between the latter two groups. In the rats in the same group, the number of BDNF-positive cells varied markedly in different brain regions (P<0.05), and the expression level of BDNF was the highest in the frontal cortex followed by the hippocampal CA3 region and the dentate gyrus, and was the lowest in the hippocampal CA1 region. Conclusion Treatment with rhEPO enhances the expression of BDNF in rat neural cells, suggesting that rhEPO may protect the nervous system from aging by regulating the BDNF pathway.