食品科学 ›› 2024, Vol. 45 ›› Issue (16): 105-112.doi: 10.7506/spkx1002-6630-20230812-085

• 营养卫生 • 上一篇    下一篇

猕猴桃皮多酚对脂多糖应激Caco-2细胞抗氧化能力的影响

徐瑞屿,薛沙,牛鸿艳,黄群,周艳   

  1. (贵州医科大学公共卫生与健康学院,环境污染与疾病监控教育部重点实验室,贵州省生态食品创制工程研究中心,贵州 贵阳 561113)
  • 出版日期:2024-08-25 发布日期:2024-08-06
  • 基金资助:
    国家自然科学基金地区科学基金项目(32060537)

Effects of Kiwifruit Peel Polyphenols on Antioxidant Capacity of Lipopolysaccharide-Stressed Caco-2 Cells

XU Ruiyu, XUE Sha, NIU Hongyan, HUANG Qun, ZHOU Yan   

  1. (Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Engineering Research Center of Ecological Food Innovation, School of Public Health, Guizhou Medical University, Guiyang 561113, China)
  • Online:2024-08-25 Published:2024-08-06

摘要: 目的:探讨猕猴桃皮多酚(kiwifruit peel polyphenols,KPP)对脂多糖(lipopolysaccharide,LPS)应激Caco-2细胞抗氧化能力的影响。方法:采用CCK-8法测定不同处理组Caco-2的细胞活力,荧光分光光度计测定活性氧和线粒体膜电位,分光光度计测定超氧化物歧化酶(superoxide dismutase,SOD)活力和谷胱甘肽(glutathione,GSH)、丙二醛(malonaldehyde,MDA)含量,实时荧光定量聚合酶链式反应测定核红细胞2相关因子2(nuclear factor erythroid 2-related factor 2,Nrf2)、Kelch样ECH相关蛋白1(Kelch-like ECH-associated protein 1,Keap1)、NAD(P)H:醌氧化还原酶1(NAD(P)H:quinone oxidoreductase 1,NQO1)、超氧化物歧化酶1(superoxide dismutase 1,SOD1)、SOD2基因的表达;蛋白印迹测定Nrf2、Keap1及NQO1蛋白表达水平。结果:与LPS组相比,经50 µg/mL KPP干预后细胞活力显著升高(P<0.05);活性氧水平和MDA含量分别显著下降至1.82±0.28、5.08 nmol/mg(P<0.05),线粒体膜电位显著升高至1.84±0.10(P<0.05),SOD活力和GSH含量分别显著升高至52.57 U/mg和69.46 µmol/g(P<0.05);同时KPP干预能显著提高Nrf2、NQO1基因和蛋白表达(P<0.05),显著降低Keap1基因和蛋白表达(P<0.05)。结论:KPP能够通过Keap1/Nrf2/NQO1信号通路提高Caco-2的抗氧化水平,缓解LPS应激造成的细胞损伤。

关键词: 猕猴桃皮多酚;脂多糖;Caco-2细胞;抗氧化活性;Nrf2通路

Abstract: Purpose: To explore the effects of kiwifruit peel polyphenols (KPP) on the antioxidant capacity of lipopolysaccharide (LPS)-stressed Caco-2 cells. Methods: The viability of Caco-2 cells in different treatment groups was determined by the cell counting kit-8 (CCK-8) assay, reactive oxygen species (ROS) and mitochondrial membrane potential by fluorescence spectrophotometry, the activity of superoxide dismutase (SOD), and the contents of glutathione (GSH) and malonaldehyde (MDA) by spectrophotometry, the gene expression of nuclear factor erythroid 2-related factor 2 (Nrf2), Kelch-like ECH-associated protein 1 (Keap1), NAD(P)H:quinone oxidoreductase 1 (NQO1), superoxide dismutase 1 (SOD1) and SOD2 by real-time quantitative polymerase chain reaction, and the protein expression levels of Nrf2, Keap1, and NQO1 by Western blot. Results: Compared with the LPS group, cell viability was elevated after 50 µg/mL KPP intervention (P < 0.05); the levels of ROS and MDA were decreased to 1.82 ± 0.28 and 5.08 nmol/mg (P < 0.05), respectively; mitochondrial membrane potential, SOD activity and GSH content were increased to 1.84 ± 0.10, 52.57 U/mg and 69.46 µmol/g (P < 0.05), respectively. Meanwhile, KPP intervention increased the gene and protein expression of Nrf2 and NQO1 (P < 0.05) and decreased Keap1 gene and protein expression (P < 0.05). Conclusion: KPP can enhance the antioxidant capacity of Caco-2 cells through the Keap1/Nrf2/NQO1 signaling pathway, thereby alleviating the cellular damage caused by LPS stress.

Key words: kiwifruit peel polyphenols; lipopolysaccharide; Caco-2 cells; antioxidant capacity; Nrf2 pathway

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