期刊文献+

大鼠胶质细胞参与D-半乳糖诱导脑衰老过程研究 被引量:3

Glial cells in the D-galactose-induced brain aging in rats
下载PDF
导出
摘要 目的:观察大鼠胶质细胞是否参与了D-半乳糖诱导的脑衰老的过程。方法:采用D-半乳糖制备动物大鼠衰老模型,生化分光光度法检测大鼠脑海马氧化应激水平,免疫组化方法观察大鼠海马星形胶质细胞和小胶质细胞的表达和形态变化。结果:大鼠模型组较对照组海马氧化应激水平增高,星形胶质细胞和小胶质细胞表达增多,染色增强。免疫荧光染色结果显示,模型组胶质细胞和诱导型一氧化氮合酶有共存关系,模型组海马一氧化氮水平升高。结论:大鼠胶质细胞可能参与了D-半乳糖诱导脑衰老的过程。 Objective: To investigate the D-gal-induced brain aging process in rat glial cells.Methods: Aging rat animal model was prepared by D-galactose,and oxidative stress levels were tested by biochemical spectrophotometry in rat hippocampus.Expression and morphological changes of hippocampal astrocytes and microglia in rat were observed by immunohistochemistry.Results: In the hippocampus,the levels of oxidative stress were increased in rat model group than that the control group,the expressions of astrocytes and microglial cells had increased and staining enhancement.Immunofluorescence staining showed that glial cells in the model group were co-localization with inducible nitric oxide synthase,and the hippocampal nitric oxide levels were increased in the model group.Conclusion: Rat glial cells may be involved in D-gal-induced brain aging process.
作者 雷鸣 朱祖健
出处 《神经解剖学杂志》 CAS CSCD 北大核心 2011年第6期675-680,共6页 Chinese Journal of Neuroanatomy
基金 江苏省教育厅2010年大学生实践创新训练计划(806) 江苏建康职业学院科技发展基金(JK201004)
关键词 D-半乳糖 胶质细胞 脑衰老 大鼠 D-galactose glial cells brain aging rat
  • 相关文献

参考文献16

  • 1Ho SC, Liu JH, Wu RY. Establishment of the mimetic aging effect in mice caused by D-galactose [ J]. Biogerontology, 2003, d:15 - 18.
  • 2Chen B, Zhong Y, Peng W, et al. damage and decreased base excision D-galactose-induced aging rats [J]. Increased mitochondrial DNA repair in the auditory cortex of Mol Biol Rep, 2011,38:3635-3642.
  • 3Li WJ, Nie SP, Xie MY, et al. Ganoderma atrum polysaccharide at- tenuates oxidative stress induced by d-galactose in mouse brain [J]. LifeSci, 2011, 88:713 -718.
  • 4Zhong SZ, Ge QH, Qu R, et al. Paeonol attenuates neurotoxicity and ameliorates cognitive impairment induced by d-galactose in ICR mice [ J]. J Neurol Sci, 2009, 277:58-64.
  • 5Ndubaku U, de Bellard ME. Glial cells: old cells with new twists [ J ]. Acta Histochem, 2008, 110 : 182 - 195.
  • 6Van Eldik LJ, Thompson WL, Ralay Ranaivo H, et al. Glia proin- flammatory cytokine upregulation as a therapeutic target for neurode- generative diseases: function-based and target-based discovery ap- proaches [ J]. Int Rev Neurobiol, 2007, 82:277 - 296.
  • 7Barzilai A. DNA damage, neuronal and glial cell death and neurode- generation [ J]. Apoptosis, 2010, 15:1371 - 1381.
  • 8Cui X, Zuo P, Zhang Q, et al. Chronic systemic D-galactose expo- sure induces memory loss, neurodegeneration, and oxidative damage in mice: protective effects of R-alpha-lipoic acid [ J]. J Neurosci Res, 2006, 83:1584 -1590.
  • 9Lei M, Su Y, Hua X, et al. Chronic systemic injection of D-galac- rose impairs the septohippocampal cholinergic system in rats [ J ]. Neuroreport, 2008, 19 : 1611 - 1615.
  • 10Wang L, Cnlodner K.I, Feany MB. Protein misfolding and oxidative stress promote glial-mediated neurodegeneration in an Alexander disease model [J]. J Neurosci, 2011, 31:2868 -2877.

同被引文献55

引证文献3

二级引证文献15

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部