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蜂胶乙醇提取物对小鼠主动脉内皮细胞损伤的保护作用
引用本文:杨博,朱宇轩,缪晓青,徐晓兰,杨文超.蜂胶乙醇提取物对小鼠主动脉内皮细胞损伤的保护作用[J].食品工业科技,2021,42(15):332-336.
作者姓名:杨博  朱宇轩  缪晓青  徐晓兰  杨文超
作者单位:1.福建农林大学食品科学学院,福建福州 3500002.福建农林大学动物科学学院(蜂学学院),福建福州 3500003.蜂产品加工与应用教育部工程中心,福建福州 350000
基金项目:现代农业蜂产业技术体系岗位科学家(CARS-45-KXJ20)
摘    要:目的:探究蜂胶乙醇提取物(ethanol extracts of propolis,EEP)对脂多糖(lipopolysaccharide,LPS)诱导的小鼠主动脉内皮细胞(mouse aortic endothelial cell,MAEC)炎症因子损伤的保护作用。方法:将细胞分为对照组,LPS模型组,蜂胶低(2.5 μg/mL)、中(5 μg/mL)、高(10 μg/mL)剂量组。采用CCK-8检测MAEC的细胞增殖率,ELISA酶联免疫吸附实验测定MAEC炎症细胞中TNF-α、IL-6的含量,Western Blot法测定MAEC炎症细胞中ICAM-1、VCAM-1、MCP-1的表达水平。结果:与对照组相比,LPS组MAEC的细胞增殖率极其显著降低(P<0.001),ICAM-1、VCAM-1、MCP-1、TNF-α以及IL-6的水平极其显著升高(P<0.001)。经不同浓度EEP处理后,MAEC的细胞增殖率显著上升(P<0.05或P<0.01),TNF-α、IL-6的含量以及ICAM-1、VCAM-1、MCP-1表达水平降低,各蜂胶组与LPS组相比均有显著性差异(P<0.01或P<0.001)。结论:EEP能够抑制LPS诱导的MAEC中炎症因子的表达,对血管内皮细胞具有保护作用。

关 键 词:蜂胶    小鼠主动脉内皮细胞    脂多糖    抗炎    炎症因子
收稿时间:2020-10-12

Protective Effects of Propolis Ethanol Extract on Mouse Aortic Endothelial Cells Injury
YANG Bo,ZHU Yuxuan,MIAO Xiaoqing,XU Xiaolan,YANG Wenchao.Protective Effects of Propolis Ethanol Extract on Mouse Aortic Endothelial Cells Injury[J].Science and Technology of Food Industry,2021,42(15):332-336.
Authors:YANG Bo  ZHU Yuxuan  MIAO Xiaoqing  XU Xiaolan  YANG Wenchao
Affiliation:1.College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350000, China2.College of Animal Science (College of Bee Science), Fujian Agriculture and Forestry University, Fuzhou 350000, China3.Bee Product Processing and Application Research Center of the Ministry of Education, Fuzhou 350000, China
Abstract:Objective: The aim of this study was to investigate the protective effects of ethanol extracts of propolis (EEP) on mouse aortic endothelial cells (MAEC) from injury induced by lipopolysaccharide (LPS). Methods: Cell proliferation rate was determined by CCK-8. Then MAEC were divided into the blank group, LPS model group, low-dose (2.5 μg/mL), middle-dose (5 μg/mL), and high-dose (10 μg/mL) groups of EEP. The TNF-α and IL-6 levels were evaluated by ELISA. The expression levels of ICAM-1, VCAM-1 and MCP-1 were measured by Western Blot. Results: Compared with the control group, the cell proliferation rate of MAEC in the LPS group was extremely significant reduced (P<0.001), and the levels of ICAM-1, VCAM-1, MCP-1, TNF-α and IL-6 were extremely significant increased (P<0.001). The cell proliferation rate of EEP groups increased significantly (P<0.05 or P<0.01), and the content of TNF-α, IL-6 and the expression levels of ICAM-1, VCAM-1, and MCP-1 decreased compared with these of LPS group. There were significant differences between each propolis group and LPS group (P<0.01 or P<0.001). Conclusion: EEP could effectively inhibit LPS-induced the expression of inflammatory factors in MAEC, and it has the effect of protecting endothelial cells.
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