林勇,刘仲华,马蕊.茶叶中表没食子儿茶素没食子酸酯抑制中波紫外线诱导HaCaT细胞氧化损伤研究[J].食品安全质量检测学报,2015,6(4):1224-1228
茶叶中表没食子儿茶素没食子酸酯抑制中波紫外线诱导HaCaT细胞氧化损伤研究
Inhibition effects of epigallocatechin gallate in tea on oxidative damage of HaCaT cells induced by ultraviolet radiation B
投稿时间:2015-03-24  修订日期:2015-04-22
DOI:
中文关键词:  表没食子儿茶素没食子酸酯  中波紫外线  HaCaT细胞  氧化损伤
英文关键词:epigallocatechin gallate  ultraviolet radiation B  HaCaT cell  oxidative damage
基金项目:教育部高校博士点专项基金项目(20114320120004)、湖南省科技计划项目(2014FJ3131)
作者单位
林勇 国家植物功能成分利用工程技术研究中心; 湖南农业大学茶学教育部重点实验室 
刘仲华 国家植物功能成分利用工程技术研究中心; 湖南农业大学茶学教育部重点实验室 
马蕊 湖南农业大学茶学教育部重点实验室; 广西职业技术学院 
AuthorInstitution
LIN Yong National Research Center of Engineering & Technology for Utilization of Botanical Functional Ingredients; Key Lab of Tea Science of Education Ministry, Hunan Agricultural University 
LIU Zhong-Hua National Research Center of Engineering & Technology for Utilization of Botanical Functional Ingredients; Key Lab of Tea Science of Education Ministry, Hunan Agricultural University 
MA Rui Key Lab of Tea Science of Education Ministry, Hunan Agricultural University; Guangxi Vocational & Technical College 
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中文摘要:
      目的 研究茶叶中表没食子儿茶素没食子酸酯(EGCG)对中波紫外线(UVB)诱导的人表皮角质形成细胞(HaCaT)光损伤的保护作用。方法 用不同浓度的EGCG对HaCaT细胞进行预处理6 h, 采用60 mJ/cm2的剂量照射细胞, 用MTT法检测细胞生存率, 吸取细胞上清液检测超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH–Px)、乳酸脱氢酶(LDH)的活性和丙二醛(MDA)含量变化, 用荧光法检测细胞内ROS含量。结果 UVB辐射对HaCaT细胞造成严重损伤, 与对照组相比, 细胞活性下降21.63%; 与UVB辐射模型组相比, EGCG尤其高剂量可提高UVB照射后HaCaT细胞的存活率5.89%, 显著提高SOD、GSH–Px活性(P<0.01), 降低LDH活性 (P<0.01), 减少自由基ROS和MDA含量(P<0.01)。结论 EGCG可以减少UVB诱导HaCaT细胞的损伤和凋亡, 具有光保护作用, 其机制与增强细胞抗氧化能力和加速清除氧自由基有关。
英文摘要:
      Objective To study the photo-protective effect of epigallocatechin gallate in tea on HaCaT cells damaged from ultraviolet radiation B. Methods Sub–confluent HaCaT cells were incubated for 6 h with different doses of EGCG, and then irradiated with 60 mJ/cm2 doses of UVB. The cell viability was tested by MTT method. The activity of superoxide dismutase (SOD), glutathione peroxidase (GSH-Px), lactate dehydro-genase (LDH), and the level of malondialdehyde (MDA) of supernatant were detected with colorimetric me-thods. The content of ROS was measured with the fluorescence method. Results Compared with control group, the UVB irradiation could seriously damage HaCaT cell and gave rise to 21.63% cell viability decline. EGCG, especially this with the high dose, could enhance cell viability by 5.89%, increase SOD and GSH-Px activity in supernatant under UVB irradiation, and decrease LDH activity and the contents of MDA and ROS in dose–dependent manner (P<0.01). Conclusion EGCG can relieve UVB-induced oxidative damage and apoptosis of HaCaT cells, which may be the reasons that they enhance the oxidase activity and clear the oxy-radicals in cells.
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