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十二碳烯酸对人H4细胞毒性作用研究
引用本文:俞发荣,连秀珍,张红梅,李世平,谢明仁. 十二碳烯酸对人H4细胞毒性作用研究[J]. 中国现代应用药学, 2014, 31(2): 134-136
作者姓名:俞发荣  连秀珍  张红梅  李世平  谢明仁
作者单位:甘肃政法学院,甘肃省证据科学研究与应用重点实验室,兰州 730070;甘肃政法学院,甘肃省证据科学研究与应用重点实验室,兰州 730070;甘肃政法学院,甘肃省证据科学研究与应用重点实验室,兰州 730070;甘肃政法学院,甘肃省证据科学研究与应用重点实验室,兰州 730070;甘肃政法学院,甘肃省证据科学研究与应用重点实验室,兰州 730070
基金项目:兰州市科技计划资助项目(2010-1-128)
摘    要:目的探讨十二碳烯酸对人H4细胞的毒性作用机制。方法采用MTT法、流式细胞仪检测十二碳烯酸对人H4细胞的毒性作用。结果分别给予人H4细胞0.3,0.9,2.7mg·L^-1十二碳烯酸培养48h,十二碳烯酸对人H4细胞增殖抑制率分别为41.64%,70.97%,81.52%,半数抑制浓度(IC50)为0.40mg·L^-1,与对照组相比,差异有统计学意义(P〈0.01);凋亡率分别为10.16%,18.22%,24.06%。结论十二碳烯酸对人H4细胞具有显著的毒性作用,其机制可能与损伤线粒体结构,抑制细胞分裂等有关。

关 键 词:十二碳烯酸  人H4细胞  毒性作用
收稿时间:2013-04-16
修稿时间:2013-08-16

Cytotoxicity of 2-Dodecenoic Acid on Human H4 Cells
YU Farong,LIAN Xiuzhen,ZHANG Hongmei,LI Shiping and XIE Mingren. Cytotoxicity of 2-Dodecenoic Acid on Human H4 Cells[J]. The Chinese Journal of Modern Applied Pharmacy, 2014, 31(2): 134-136
Authors:YU Farong  LIAN Xiuzhen  ZHANG Hongmei  LI Shiping  XIE Mingren
Affiliation:Gansu Institute of Political Science and Law, Key Laboratory of Evidence of Science and Technology Research and Application, Lanzhou 730070, China;Gansu Institute of Political Science and Law, Key Laboratory of Evidence of Science and Technology Research and Application, Lanzhou 730070, China;Gansu Institute of Political Science and Law, Key Laboratory of Evidence of Science and Technology Research and Application, Lanzhou 730070, China;Gansu Institute of Political Science and Law, Key Laboratory of Evidence of Science and Technology Research and Application, Lanzhou 730070, China;Gansu Institute of Political Science and Law, Key Laboratory of Evidence of Science and Technology Research and Application, Lanzhou 730070, China
Abstract:OBJECTIVE To study 2-dodecenoic acid toxicity mechanism on human H4 cells. METHODS Toxic effects of 2-dodecenoic acid on human H4 cells were detected with methods of MTT and flow cytometry. RESULTS Given the human H4 cells 0.3, 0.9, 2.7 mg·L-1 2-dodecenoic acid for 48 h, human H4 cells proliferation inhibition rates were 41.64%, 70.97%, 81.52%, respectively, and the 50% inhibitory concentration(IC50) was 0.40 mg·L-1, compared with the control group, the difference was statistically significant(P<0.01); apoptosis rates were 10.16%, 18.22%, 24.06%, respectively. CONCLUSION 2-Dodecenoic acid on human H4 cells has significant toxic effects, its mechanism may be related to the destruction of the cell mitochondrial structure and inhibition of cell division.
Keywords:2-dodecenoic acid   human H4 cells   toxic effects
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