摘要
目的探讨姜黄索对β淀粉样蛋白(Aβ)25~35诱导的PC12细胞损伤的保护作用。方法采用不同浓度的Aβ25~35处理分化后的PC12细胞,同时应用姜黄素进行干预,采用四甲基偶氮唑盐法检测细胞活力及代谢状态,采用磷脂酰丝氨酸外翻法检测细胞凋亡,采用流式细胞仪检测细胞凋亡率。结果Aβ25~35处理24h后,PC12细胞活力显著下降,且呈剂量依赖性。姜黄素(5~20μmol/L)对Aβ25~35诱导的细胞凋亡具有明显的抑制作用。与仅以20μmol/L Aβ25~35处理相比,5μmol/L姜黄素+20μmol/L Aβ25~35处理后的细胞凋亡百分比明显降低(P<0.01)。结论Aβ25~35能够诱导PC12细胞凋亡,姜黄素对其诱导的PC12细胞凋亡具有保护作用。
Objective To investigate the protective effect of Curcumin on apoptosis of PC12 cells induced by β amyloid(Aβ) 25-35. Methods Differentiated PC12 cells were treated with different concentrations of Aβ25-35 and Curcumin for 24 h. Cell viability was measured by MTT assay and cell apoptosis was detected by Annexin-V staining and flow cytometry. Results The cell viability was significantly decreased 24 h after treatment with Aβ25-35 ( P 〈 0.01 ); the decrease was in a dose-dependent manner. Curcumin (5-20 μmol/L) showed obvious inhibitory effect on the apoptosis induced by Aβ25-35. Compared with Aβ25-35 (20 μmol/L) group, cell apoptosis in Curcmin (5 μmol/L) plus Aβ25-35 (20 μmol/L) group was significantly lower ( P 〈 0. 01 ). Conclusion Aβ25-35 can induce neuronal apoptosis and Cucumin can antagonize the cell apoptosis induced by Aβ25-35. (Shanghai Med J, 2007, 30:843-846)
出处
《上海医学》
CAS
CSCD
北大核心
2007年第11期843-846,共4页
Shanghai Medical Journal
基金
国家重点基础研究发展计划(973计划)资助项目(2006CB500700)
上海市医学领军人才计划资助项目(LJ06003)