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乙苯对HEI-OC1细胞增殖及氧化应激水平的影响
引用本文:刘可平,苏艺伟,张晋蔚,王致,马雨莹,刘移民,肖勇梅.乙苯对HEI-OC1细胞增殖及氧化应激水平的影响[J].中华劳动卫生职业病杂志,2021(1):44-47.
作者姓名:刘可平  苏艺伟  张晋蔚  王致  马雨莹  刘移民  肖勇梅
作者单位:广州医科大学附属市十二人民医院;广州市职业病防治院;中山大学公共卫生学院劳动卫生与环境卫生学系
基金项目:国家自然科学基金(81973006、81573123);广州市医学重点学科建设项目(穗卫科教[2016]27号);广州市高水平临床重点专科建设项目(穗卫[2019]1555号);广州市"121人才梯队工程"后备人才项目(穗人社发[2011]167号);广州市卫生健康科技项目(20191A010037)。
摘    要:目的研究乙苯染毒后耳蜗毛细胞株(HEI-OC1)细胞增殖及氧化指标的变化。方法于2019年7至12月,设置乙苯浓度分别为0、30、60、90、300、600、900 μmol/L和3、6、9、10 mmol/L,共11个浓度组,用CCK-8法测定乙苯染毒24 h后HEI-OC1细胞增殖活性;以0、1、2、4、8、16、32、64 mmol/L乙苯处理细胞24 h,计算乙苯的半数抑制浓度。用0、6、9和12 mmol/L乙苯染毒HEI-OC1细胞24 h后,测定细胞内丙二醛(MDA)含量、超氧化物歧化酶(SOD)和谷胱甘肽过氧化物酶(GSH-Px)活力。结果与0 mmol/L浓度组比较,6、9、12 mmol/L浓度HEI-OC1细胞存活率明显降低(P<0.01)。乙苯对HEI-OC1细胞的半数抑制浓度为12.86 mmol/L(R2=99.05)。不同浓度组(0、6、9、12 mmol/L)乙苯处理HEI-OC1细胞24 h,MDA含量、SOD和GSH-Px活力差异均有统计学意义(F=65.11、6.48、22.85,P<0.05);与0 mmol/L浓度组比较,9、12 mmol/L浓度组HEI-OC1细胞MDA含量明显升高,12 mmol/L浓度组SOD活力明显降低,6、12 mmol/L浓度组GSH-Px活力明显降低,差异均有统计学意义(P<0.05)。结论乙苯可以抑制HEI-OC1细胞增殖,引起细胞氧化损伤。

关 键 词:细胞增殖  氧化性应激  乙苯  耳蜗  毛细胞  听觉  存活率

The effects of ethylbenzene on HEI-OC1 cells proliferation and oxidative stress level
Liu Keping,Su Yiwei,Zhang Jinwei,Wang Zhi,Ma Yuying,Liu Yimin,Xiao yongmei.The effects of ethylbenzene on HEI-OC1 cells proliferation and oxidative stress level[J].Chinese Journal of Industrial Hygiene and Occupational Diseases,2021(1):44-47.
Authors:Liu Keping  Su Yiwei  Zhang Jinwei  Wang Zhi  Ma Yuying  Liu Yimin  Xiao yongmei
Institution:(Guangzhou Twelfth People's Hospital Affiliated to Guangzhou Medical University,Guangzhou 510620,China;Guangzhou Occupational Disease Prevention and Treatment Hospital,Guangzhou 510620,China;Department of Labor and Environmental Hygiene,School of Public Health,Sun Yat-sen University,Guangzhou 510080,China)
Abstract:Objective To study the changes of proliferation and oxidation indexes of Cochlear hair cell line(HEI-OC1 cells)exposed to ethylbenzene.Methods From July to December 2019,11 groups with ethylbenzene concentrations of 0,30,60,90,300,600,900μmol/L and 3,6,9,10 mmol/L,were used to determine the proliferation activity of HEI-OC1 cells exposed to ethylbenzene for 24 hours,and the cells were treated with 0,1,2,4,8,16,32,64 mmol/L ethylbenzene for 24 hours,then the 50%inhibitory concentration of ethylbenzene was calculated.After HEI-OC1 cells were exposed to 0,6,9 and 12 mmol/L ethylbenzene for 24 hours,the malondialdehyde(MDA)content,superoxide dismutase(SOD)and glutathione peroxidase(GSH-Px)activities were measured.Results Compared with 0 mmol/L concentration group,the survival rate of HEI-OC1 cells at 6,9,12 mmol/L concentration was significantly decreased(P<0.01).The 50%inhibitory concentration of ethylbenzene on HEI-OC1 cells was 12.86 mmol/L(R2=99.05).There were significant differences in SOD and GSH-Px activity in HEI-OC1 cells treated with ethylbenzene at different concentrations(0,6,9,12 mmol/L)for 24 hours(F=65.11,6.48,22.85,P<0.05).Compared with 0 mmol/L concentration group,the MDA content of HEI-OC1 cells was significantly increased in 9 and 12 mmol/L concentration groups,the SOD activity was significantly decreased in 12 mmol/L concentration group,and the GSH-Px activity was significantly decreased in 6 and 12 mmol/L concentration groups.Conclusion Ethylbenzene can inhibit the proliferation of HEI-OC1 cells and cause oxidative damage.
Keywords:Cell proliferation  Oxidative stress  Ethylbenzene  Cochlea  Hair cells  auditory  Survival rate
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