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地塞米松对嘧啶亚硝脲诱导人脑胶质瘤细胞凋亡的影响
引用本文:廖旭兴,刘泉开,柳结,洪涛.地塞米松对嘧啶亚硝脲诱导人脑胶质瘤细胞凋亡的影响[J].中国临床神经外科杂志,2009,14(4):228-230.
作者姓名:廖旭兴  刘泉开  柳结  洪涛
作者单位:1. 广州军区武汉总医院神经外科,湖北武汉,430070
2. 南昌大学第一附属医院神经外科,江西南昌,330006
3. 江西省人民医院中心实验室,江西南昌,330006
摘    要:目的观察地塞米松(DEX)对嘧啶亚硝脲(ACNU)诱导的人脑胶质瘤细胞凋亡的影响。方法分别以ACNU、DEX、ACNU联合DEX,作用于体外培养的人脑胶质瘤细胞系SHG—4460h,通过细胞形态学及流式细胞仪分析检测细胞凋亡。结果①形态学观察:ACNU组、ACNU联合DEX组,大部分瘤细胞呈现细胞凋亡的形态学改变。而DEX组及正常对照组仅个别细胞出现上述形态改变。②荧光显微镜观察及流式细胞仪分析:ACNU组、ACNU联合DEX组有典型的凋亡峰,且其瘤细胞的凋亡率明显高于DEX组及正常对照组瘤细胞的凋亡率(P〈0.01),但ACNU组的SHG~44细胞的凋亡率与ACNU联合DEX组相差不显著(P〉0.05)。结论DEX对ACNU诱导人脑胶质瘤细胞凋亡没有明显影响。

关 键 词:人脑胶质瘤  地塞米松  嘧啶亚硝脲  凋亡  细胞培养

Effect of Dexamethasone on Apoptosis of Human Brain Glioma Cells Induced by Nimustine in Vitro
Institution:LIAO Xu-xing, LIU Quan-kai, LIU Zhe, et al.(Department of Neurosurgery, Wuhan General Hospital, Guangzhou Command, PLA , Wuhan Hubei 430070, China)
Abstract:Objectives To observe the effect of the Dexamethasone(DEX)on apoptosis of human brain gliomas cells induced by Nimustine hydrochloride (ACNU) in vitro.Methods Human malignant glioma cell lines SHG-44 cells,which were cultured,were exposed to ACNU,DEX and ACNU combined with DEX respectively for 60 hours in vitro.Then Apoptosis Rate of SHc-44 cells were determined by morphological technique and flow cytometry analysis.Results The morphological study showed that the apoptosis of most of SHG-44 cells occurred in both ACNU and ACNU combined DEX groups.and the apeptosis of only few SHG-44 cells occunrred in DEX group.The flow cytometry analysis showed that the apoptosis rates of SHG-44 cells in both the ACNU and ACNU combined with DEX groups,where the typical apoptotic peak was found,were significantly higher than those in DEX group and the normal control group(P<0.01).There was insignificant diference in the rate of the apoptosis of SHG-44 cells between both the ACNU and ACNU combined DEX groups(P>0.05).Conclusion There was insignificant effect of DEX on apoptosis of SHC-44 cells induced by ACNU.
Keywords:Human brain glioma  Dexamethasone  Nimustine hydrochloride  Apoptosis  Cell culture
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