详细信息
鱼藤素降低小鼠神经母细胞瘤细胞Neuro-2A存活率的实验研究 被引量:1
Inhibitory Effects of Deguelin on the Viability of Neuro-2A Cells
文献类型:期刊文献
中文题名:鱼藤素降低小鼠神经母细胞瘤细胞Neuro-2A存活率的实验研究
英文题名:Inhibitory Effects of Deguelin on the Viability of Neuro-2A Cells
作者:熊中奎[1,2];王思本[1];郎娟[3]
机构:[1]绍兴第二医院放疗科;[2]绍兴文理学院医学院临床医学部;[3]绍兴市人民医院医学研究中心
年份:2014
卷号:0
期号:11
起止页码:1793
中文期刊名:中国药师
外文期刊名:China Pharmacist
收录:CSTPCD
基金:浙江省自然科学基金(编号:Y2100035);浙江省中医药科技计划(编号:2011ZA108;2012ZB162);浙江省医药卫生科技计划(编号:2014KYB286)
语种:中文
中文关键词:鱼藤素;Neuro-2A细胞;细胞存活率;caspase;3
外文关键词:Deguelin;Neruo-2A cell;Cell viability
中文摘要:目的:研究鱼藤素对小鼠神经母细胞瘤细胞Neuro-2A(N2A)存活率及凋亡的影响。方法:N2A细胞以5×10^4·ml^-1密度接种到细胞培养板中,1×10^-8mol·L^-1鱼藤素处理后6,12,24,48,72 h等5个时间点上测定细胞存活率;加入鱼藤素0,1×10^-11,1×10^-10,1×10^-9,1×10^-8,1×1^0-7,1×10^-6mol·L^-1等7个不同浓度干预48 h后测定细胞存活率。2×10^-8mol·L^-1鱼藤素干预24 h,测定细胞匀浆中caspase 3活力。结果:5×10^4·ml^-1N2A细胞以含10%胎牛血清DMEM培养基培养,第48 h达到细胞生长曲线的峰值。1×10^-8mol·L^-1鱼藤素干预24-72 h,时间依赖性显著降低N2A细胞存活率(P〈0.05);在鱼藤素干预48 h时间点上,1×10^-8-1×10^-6·mol·^L-1浓度范围内剂量依赖性可显著降低N2A细胞存活率(P〈0.05),其IC50=1.6×10^-8mol·L^-1。鱼藤素作用于N2A细胞24 h可显著提高caspase 3活力,约达到对照组的5.6倍。结论:鱼藤素可时间依赖性且剂量依赖性降低N2A细胞存活率,可能与增加caspase 3活力有关。
外文摘要:Objective:To investigate the effects of deguelin on the viability and apoptosis of Neuro-2A ( N2A) cells. Methods:The cell viability of N2A cells with the density of 5 × 10^4 ·ml^-1 on the time points of 6, 12, 24, 48 and 72 hours after 1 × 10^ -8 mol ·L^-1 deguelin treatment using CCK-8 kits was determined, and that on the time point of 48 hours after 0, 1 × 10^ -11 , 1 × 10^ -10 , 1 × 10 ^-9 , 1 × 10 ^-8 , 1 × 10^ -7 , 1 × 10 ^-6 or 5 × 10^ -4 mol·L^-1 deguelin treatment was also detected. The activity of caspase 3 was determined in N2A cells treated by 2 × 10^ -8 mol·L^-1 deguelin for 24 hours. Results:N2A cells with the density of 5 × 10^4 ·ml^-1 reached the peak level in the growth curve 48 hours after the incubation in DMEM medium with 10% fetal bovine serum. The cell viability of N2A cells was decreased after the treatment of 1 × 10 ^-8 mol·L^-1 deguelin for 24-72 hours in a time-dependant manner or after the treatment of 1 × 10^ -8 -1 × 10^ -6 mol·L^-1 deguelin for 48 hours in a dose-dependant manner (P〈0. 05) with IC50 of 1. 6 × 10 ^-8 mol ·L^-1 . The activity of caspase 3 was increased after the treatment of 2 × 10^ -8 mol·L^-1 deguelin for 24 hours, which was 5. 6-fold of that in the control group. Conclusion: Cell viability of N2A cells is inhibited by deguelin in a time- and dose-dependent manner, which may be related to the activity increase of caspase 3.
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