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作 者:张凤军[1] 王丽红[1] 刘真[1] 邢子英[1] 王怀经[1] 李振中[1]
机构地区:[1]山东大学医学院解剖学教研室,济南250012
出 处:《山东大学学报(医学版)》2009年第4期38-41,45,共5页Journal of Shandong University:Health Sciences
基 金:山东省自然科学基金重点项目(Z2006D05;Z2006C06)
摘 要:目的探测胰岛素样生长因子-1(IGF-1)对背根神经节(DRG)神经元谷氨酸(Glu)损伤的保护作用。方法Wistar胎鼠DRG神经元分散培养48h后,用Glu(200μmol/L)造成神经元损伤,并同时给予IGF-1(10nmol/L),观察添加IGF-1和未添加IGF-1孵育的Glu损伤的神经元的活细胞生长状况,并用流式细胞仪检测神经元的凋亡率,用共聚焦激光扫描显微镜(CLSM)检测细胞内钙离子荧光强度。结果用IGF-1孵育的神经元生长状况良好,凋亡率、细胞内钙离子荧光强度均低于无IGF-1孵育的标本。结论IGF-1可通过减低钙离子内流,抑制细胞凋亡,从而对Glu损伤的DRG神经元产生保护作用。Objective To determine the neuro-protective effects of insulin-like growth factor 1 (IGF-1) on cultured dorsal root ganglion (DRG) neurons injured by glutamate (Glu). Methods DRG neurons of Wistar rat embryos were cultured for 48 h in vitro and then exposed to Glu (200 μmol/L) with or without IGF-1 ( 10 nmol/L). The living cells were observed with an inverted contrast microscope. The cultures were processed for detecting the apoptosis rate using flow cytometry and for detecting the fluo- rescent intensity of intracellular Ca^2+ using confocal laser scanning microscopy (CLSM). Results Survival status of the DRG cells with IGF-1 incubation was better than that without IGF-1 incubated cultures. The apoptosis rate and fluorescent intensity of Ca^2+ were lower in cultures with IGF-1 than those without. Conclusion IGF-1 may reduce intracellular Ca^2+ concentration, in- hibits neuronal apeptosis, and protects the DRG neurons from neurotoxicity induced by Glu.
关 键 词:胰岛素样生长因子-1 神经节 神经元 谷氨酸 大鼠 WISTAR
分 类 号:R322.85[医药卫生—人体解剖和组织胚胎学] R-332[医药卫生—基础医学]
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