天然产物研究与开发 ›› 2024, Vol. 36 ›› Issue (9): 1464-1471.doi: 10.16333/j.1001-6880.2024.9.002

• 研究论文 • 上一篇    下一篇

益生菌发酵黄芪对LPS诱导的人正常结肠上皮细胞NCM-460氧化损伤保护作用的机制研究

王   萍1,王长福2,韩士林1,匡海学1,王秋红1,2*   

  1. 1黑龙江中医药大学 教育部北药基础与应用研究重点实验室,哈尔滨 150001;2广东药科大学 广东省中药饮片规范化炮制工程技术研究中心,广州510006
  • 出版日期:2024-09-25 发布日期:2024-09-25
  • 基金资助:
    国家重点研发计划中医药现代化研究重点专项(2018YFC1707100);2022年全国名老中医药专家传承工作室建设项目(国中医药人教函〔2022〕75号);黑龙江省教育厅“头雁”团队支持项目(黑龙江省头雁行动领导小组文件〔2019〕5号)

Mechanism of the protective effect of probiotic fermented Astragali Radix on lipopolysaccharide-induced oxidative damage in normal human colon epithelial cell NCM-460

WANG Ping1,WANG Chang-fu2,HAN Shi-lin1,KUANG Hai-xue1,WANG Qiu-hong1,2*   

  1. 1Key Laboratory of Basic and Application Research of Beiyao Ministry of Education,Heilongjiang University of Chinese Medicine,Harbin 150040,China;2Guangdong Engineering Technology Research Center of Traditional Chinese Medicine of Chinese Materia Medica,Guangdong Pharmaceutical University,Guangzhou 510006,China
  • Online:2024-09-25 Published:2024-09-25

摘要:

探究益生菌发酵黄芪(fermented Astragali Radix,F-As)与黄芪(Astragali Radix,As)对脂多糖(lipopolysaccharide,LPS)诱导的肠道细胞NCM-460氧化损伤的保护作用及其分子机制。利用MTT法确定了LPS、As和F-As的工作浓度;分别检测并比较了LPS组、As + LPS组和F-As + LPS组,细胞中氧化应激相关指标、抗氧化相关基因在转录水平和蛋白水平表达的变化。与Con组相比,LPS组的活性氧(reactive oxygen species,ROS)和丙二醛(malondialdehyde,MDA)增加(P<0.01),而细胞的存活率、谷胱甘肽(glutathione,GSH)、超氧化物歧化酶(superoxide dismutase,SOD)、总抗氧化能力(total antioxidant capacity,T-AOC)以及细胞中的抗氧化基因在转录水平和蛋白水平均显著降低(P<0.01);而As + LPS组和F-As + LPS组,细胞中的ROS和MDA水平降低(P<0.01),细胞的存活率GSH、SOD、T-AOC以及抗氧化基因在转录和蛋白水平得到恢复(P<0.01),且与As + LPS组相比,F-As + LPS组恢复得更显著(P<0.05)。研究结果提示,As和F-As均可以通过激活抗氧化基因的表达,清除细胞内过多的ROS和MDA,从而对LPS诱导的细胞氧化损伤起到保护作用,且F-As优于As。

关键词: 黄芪, 益生菌发酵, 脂多糖, NCM-460细胞, 氧化损伤

Abstract:

This study aims to explore the protective effects and molecular mechanisms of probiotic fermented Astragali Radix (F-As) and non-fermented Astragali Radix (As) on the oxidative damage in lipopolysaccharide (LPS)-induced normal human colon epithelial cell NCM-460.The working concentrations of LPS,As and F-As were determined by MTT assay.The changes of oxidative stress-related indexes and antioxidant-related genes at transcription level and protein level in LPS group,As + LPS group and F-As + LPS group were detected and compared respectively.Compared with the control group,reactive oxygen species (ROS) and malondialdehyde (MDA) were significantly increased (P<0.01) after treatment of LPS,while cell viability,glutathione (GSH),superoxide dismutase (SOD),total antioxidant capacity (T-AOC) and antioxidant-related genes were decreased (P<0.01).Compared with the LPS group,As + LPS group and F-As + LPS group,the content of ROS and MDA were obviously decreased (P<0.01),whereas the content of GSH,SOD,T-AOC and antioxidant-related genes were increased (P<0.01),compared with the LPS group.However,compared with As group,F-As showed a more significant effect on enhancing these bio-indicators as mentioned above (P<0.05).The results suggest that both As and F-As can remove excessive ROS and MDA in cells by activating the expression of antioxidant genes,thus playing a protective role in LPS-induced oxidative damage of cells,and F-As is superior to As.

Key words: Astragali Radix, probiotic ferment, lipopolysaccharide, NCM-460 cells, oxidative damage

中图分类号:  R93