食品科学 ›› 2025, Vol. 46 ›› Issue (23): 215-224.doi: 10.7506/spkx1002-6630-20250624-164

• 营养卫生 • 上一篇    

甜叶菊提取物异绿原酸对过氧化氢诱导的肠上皮细胞损伤的保护作用

程文丽,郝庆红,袁宇婷,赵鹏宇,钱周泽,郭云霞,田益玲   

  1. (1.河北农业大学食品科技学院,河北 保定 071001;2.河北农业大学生命科学学院,河北 保定 071001;3.晨光生物科技集团股份有限公司,河北 邯郸 057250)
  • 发布日期:2025-12-26
  • 基金资助:
    河北省农业联合基金重点项目(C2023204144);“十四五”国家重点研发计划重点专项(2023ZD0405102); 现代农业产业技术体系建设专项(CARS-40-21);河北省农业科技推广项目(冀农科22054)

Protective Effect of Isochlorogenic Acid Extracted from Stevia rebaudiana against Hydrogen Peroxide-Induced Intestinal Epithelial Cell Injury

CHENG Wenli, HAO Qinghong, YUAN Yuting, ZHAO Pengyu, QIAN Zhouze, GUO Yunxia, TIAN Yiling   

  1. (1. College of Food Science and Technology, Hebei Agricultural University, Baoding 071001, China; 2. College of Life Sciences, Hebei Agricultural University, Baoding 071001, China; 3. Chenguang Biotech Group Co. Ltd., Handan 057250, China)
  • Published:2025-12-26

摘要: 目的:研究甜叶菊提取物异绿原酸(isochlorogenic acid,ICGA)对氧化应激损伤肠道的缓解效果。方法:采用福林酚比色法检测甜叶菊提取物中总多酚的含量;高效液相色谱法分析甜叶菊提取物中ICGA含量;细胞毒性实验(cell counting kit-8,CCK-8)和试剂盒检测丙二醛(malondialdehyde,MDA)、总抗氧化能力(total antioxidant capacity,T-AOC)、过氧化氢酶(catalase,CAT)、超氧化物歧化酶(superoxide dismutase,SOD)和谷胱甘肽过氧化物酶(glutathione peroxidase,GSH-Px)活性,筛选H2O2作用浓度和时间,并以此构建肠上皮细胞氧化应激损伤模型;通过CCK-8筛选甜叶菊提取物ICGA的安全范围和缓解猪小肠上皮细胞(intestinal porcine epithelial cell J2,IPEC-J2)细胞氧化应激损伤的适宜浓度;以抗氧化指标(MDA、T-AOC、CAT、SOD和GSH-Px)、紧密连接蛋白基因(Claudin-1、ZO-1、Occludin)、抗凋亡基因Bcl-2和促凋亡基因Caspase-3的mRNA相对表达量,明确甜叶菊提取物ICGA对肠道上皮细胞氧化应激损伤的保护作用。结果:甜叶菊提取物中总多酚的质量分数达67.68%,且3 种ICGA同分异构体总质量分数达64.23%;经200 μmol/L H2O2处理1 h建立肠道细胞氧化应激损伤模型,此时细胞存活率和抗氧化活性显著下降(P<0.05);与模型组相比,甜叶菊提取物ICGA预处理组(50 μmol/L和100 μmol/L)中细胞存活率分别从77.49%增加到90.23%和95.99%,且CAT、SOD活力和T-AOC显著增加,而MDA含量显著下降(P<0.05)。甜叶菊提取物ICGA预处理均显著提升了细胞中Claudin-1和Occludin的mRNA相对表达量(P<0.05),细胞中Caspase-3的mRNA相对表达量显著降低(P<0.05);且100 μmol/L的甜叶菊提取物ICGA组效果更好。综上,甜叶菊提取物ICGA可能通过提高抗氧化酶的活性、降低脂质过氧化物累积、改善肠道通透性以提高肠道屏障功能缓解肠道氧化应激。

关键词: 甜叶菊提取物;异绿原酸;肠道健康;过氧化氢;氧化应激

Abstract: Objective: To investigate the alleviating effect of isochlorogenic acid (ICGA) from Stevia rebaudiana on oxidative stress-induced intestinal damage. Methods: The total polyphenol content in the S. rebaudiana extract was determined using the Folin-Ciocalteu colorimetric method, and the ICGA content was analyzed via high performance liquid chromatography (HPLC). The cell counting kit-8 (CCK-8) assay and biochemical kits were employed to measure the levels of malondialdehyde (MDA), total antioxidant capacity (T-AOC), catalase (CAT), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px). The optimal H2O2 concentration and treatment time were determined to establish an intestinal epithelial cell of oxidative stress injury. The safe concentration range of ICGA and its optimal protective concentration against H2O2-induced oxidative damage in intestinal porcine epithelial cells-jejunum 2 (IPEC-J2) were selected using the CCK-8 assay. The protective effects of S. rebaudiana ICGA on intestinal epithelial cells under oxidative stress were evaluated by assessing antioxidant indicators (MDA, T-AOC, CAT, SOD, and GSH-Px) and the relative mRNA expression levels of tight junction protein genes (Claudin-1, ZO-1, and Occludin), the anti-apoptotic gene Bcl-2, and the pro-apoptotic gene Caspase-3. Results: The total polyphenol content in the S. rebaudiana extract was 67.68%, and the total content of three ICGA isomers was 64.23%. An intestinal oxidative stress injury model with significantly decreased cell viability and antioxidant activity (P < 0.05) was established by treating the cells with 200 μmol/L H2O2 for 1 hour. Compared with the model group, the cell viability in the 50 and 100 μmol/L ICGA pretreatment groups increased from 77.49% to 90.23% and 95.99%, respectively. Additionally, the activities of CAT, SOD, and T-AOC were significantly enhanced, and the MDA content was markedly reduced (P < 0.05). ICGA pretreatment significantly up-regulated the relative mRNA expression of Claudin-1 and Occludin (P < 0.05), and significantly down-regulated the expression of Caspase-3 (P < 0.05), this effect being more pronounced at 100 μmol/L than at 50 μmol/L. In conclusion, S. rebaudiana ICGA may alleviate intestinal oxidative stress by enhancing antioxidant enzyme activity, reducing lipid peroxide accumulation, and improving intestinal permeability to enhance barrier function.

Key words: Stevia rebaudiana extract; isochlorogenic acid; gut health; hydrogen peroxide; oxidative stress

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