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作 者:李熙东[1] 赵春玉[1] 隋汝波[1] 高永良[2] 赵宝东[3] 刘兴
机构地区:[1]锦州医学院附属第一医院神经内科,辽宁省锦州市121000 [2]锦州市中心医院,辽宁省锦州市121000 [3]锦州医学院解剖学教研室,辽宁省锦州市121000 [4]锦州市红十字血站,辽宁省锦州市121000
出 处:《中国临床康复》2005年第45期32-33,共2页Chinese Journal of Clinical Rehabilitation
摘 要:目的:观察辅酶Q10在以PC12细胞建立的多巴胺神经元凋亡细胞模型中的作用。方法:实验于2003-04/2004-04在锦州医学院科技试验中心进行。取体外培养的PC12细胞分为3组:①辅酶Q10组:加450μmol/L辅酶Q10和0.3mmol/L多巴胺。②多巴胺组:加0.3mmol/L多巴胺。③空白对照组:只加等量RPMI1640。24h后进行流式细胞仪测试DNA含量,检测细胞凋亡率。结果:多巴胺组细胞凋亡率明显高于空白对照组[(30.66±1.90)%,(0.82±0.07)%,P<0.01],辅酶Q10组细胞凋亡率[(16.05±2.16)%]明显低于多巴胺组(P<0.01)。结论:辅酶Q10能显著降低多巴胺引起的PC12细胞凋亡,提示辅酶Q10作为神经保护性药物对保护多巴胺能神经元,防治帕金森病可能有实际应用价值。AIM:To observe the effect of coenzyme Q10 (Co Q10) on the model of dopaminergic neuron apoptosis based on PC12 cell. METHODS:The experiment was done in the Experimental Center of Science and Technology at Jinzhou Medical College from April 2003 to April 2004.The PC12 cells, cultured in vitro, were divided into 3 groups:(1) Co Q10 group:450 μmol/L Co Q10 and 0.3 mmol/L Dopamine (DA) was added to culture medium; (2)DA group:0.3 mmol/L DA was added to culture medium; (3)Control group:RPM11640 of same dose was added to culture medium. After 24 hours, the content of DNA was tested with flow cytometer and the apoptosis rate was detected. RESULTS:The apoptosis rate in groups of Co QlO [(16.05±2.16)%] and Control [(0.82±0.07)%] were remarkably lower than that of DA group [(30.66±1.90)%](P 〈 0.01 ). CONCLUSION:Co Q10 can significantly reduce the PC12 apoptosis induced by DA. It is indicated that Co Q10, as a neuroprotective drug, possibly has an application value in the protection of dopaminergic neuron and the treatment of Parkinson disease.
分 类 号:R742.5[医药卫生—神经病学与精神病学]
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