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作 者:叶艳[1] 罗蔚锋[1] 朱婷鸽[1] 杨亚萍[1] 周旭平[1] 刘春风[1] 包仕尧[1]
出 处:《中国临床神经科学》2010年第2期135-139,共5页Chinese Journal of Clinical Neurosciences
基 金:苏州市科技计划(社会发展及医药)项目;江苏省高校自然研究计划项目(编号:08KJB320012)
摘 要:目的:评价尿酸减轻6-羟基多巴胺(6-OHDA)对PC12细胞的毒性作用。方法:应用PC12细胞制作帕金森细胞模型,分为对照组、尿酸组、6-OHDA组、尿酸+6-OHDA组。采用MTT测定各组PC12细胞活性,免疫荧光法观察各组PC12细胞caspase-3激活情况,流式细胞术检测各组PC12细胞凋亡率。尿酸100~400μmol·L^(-1)不影响PC12细胞生存率,尿酸100~400μmol·L^(-1)可显著提高6-OHDA 50μmol·L^(-1)作用6、12和24 h造成的PC12细胞生存率的下降(P<0.01);尿酸能减少6-OHDA导致的PC12细胞caspase-3激活,降低6-OHDA导致的凋亡率(P<0.05)。结论:尿酸具有减轻6-OHDA对PC12细胞的毒性作用。Aim: To investigate the protective effect of uric acid(UA) on the injury of PC12 cells induced by 6-hydroxydopamine(6-OHDA). Methods: PC12 cells injured by 6-OHDA were used as the Parkinson' s disease cell models, which were divided into four groups: control group, UA group, 6-OHDA group and UA+6-OHDA group. The cell viability were assesseded by MTT method. The apoptosis of cells were assessed by observing the caspase-3 protein level by using immunocytochemistry, and calculating apoptosis rate using flow cytometry(FCM) technique. Results: 50 μmol·L-1 of 6-OHDA decreased the viability of PC12 cells at 6, 12, 24 h. 100-400μmol·L-1 of UA had no significant effect on the viability of PC12 cells. 100-400μmol·L-1 of UA reversed the decease of PC 12 cells induced by 6-OHDA. The caspase-3 protein level and apoptosis rate of PC12 cell were increased after 6-OHDA(50 ~tmol-L 1) treatment for 24 h, which were decreased by UA(200 μmol·L-1) treatment (P〈0.05). Conclusion: 6-OHDA can decrease the viability of PC 12 cells and increase the apoptosis of PC12 cells. UA can protect PC12 cells from injury induced by 6-OHDA.
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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