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[重组人促红细胞生成素对衰老大鼠不同脑区脑源性神经营养因子表达的影响]

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

作者信息

Wang Hu-Qing, Gao Zhen, Chen Meng-Yi, Wu Hai-Qin, Zhang Gui-Lian, Zhan Shu-Qin, Bu Ning, Liu Jing-Jie, Zhai Yue-Fen

机构信息

Department of Neurology, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an 710004, China. E-mail:

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2016 Apr 20;37(4):551-554. doi: 10.3969/j.issn.1673-4254.2017.04.23.

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.

摘要

目的

探讨重组人促红细胞生成素(rhEPO)对衰老大鼠不同脑区脑源性神经营养因子(BDNF)表达的影响。

方法

将40只雄性SD大鼠随机均分为阴性对照组、D-半乳糖组、EPO治疗组和阳性对照组。通过连续皮下注射5% D-半乳糖建立亚急性衰老大鼠模型。采用免疫组织化学染色分析不同处理的衰老大鼠不同脑区BDNF表达的变化。

结果

不同组大鼠BDNF表达存在明显的脑区特异性差异。与阴性对照组相比,D-半乳糖组海马CA1区、CA3区、齿状回(DG)和额叶皮质中BDNF阳性细胞数量均明显减少(P<0.05),而EPO组和阳性对照组均增加(P<0.05),后两组间无显著差异。同一组大鼠中,不同脑区BDNF阳性细胞数量差异显著(P<0.05),BDNF表达水平在额叶皮质最高,其次为海马CA3区和齿状回,在海马CA1区最低。

结论

rhEPO治疗可增强大鼠神经细胞中BDNF的表达,提示rhEPO可能通过调节BDNF途径保护神经系统免受衰老影响。

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Erythropoietin: still on the neuroprotection road.促红细胞生成素:仍在神经保护的道路上。
Ther Adv Neurol Disord. 2012 May;5(3):161-73. doi: 10.1177/1756285611434926.
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Role of the brain-derived neurotrophic factor at glutamatergic synapses.脑源性神经营养因子在谷氨酸能突触中的作用。
Br J Pharmacol. 2008 Mar;153 Suppl 1(Suppl 1):S310-24. doi: 10.1038/sj.bjp.0707509. Epub 2007 Dec 3.

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