吉林大学学报(医学版) ›› 2026, Vol. 52 ›› Issue (5): 1302-1308.doi: 10.13481/j.1671-587X.20260512

• 基础研究 • 上一篇    

人参皂苷Rg3对高糖诱导人肾小管上皮细胞HK2损伤的改善作用及其机制

曲萌1,张亭轩1,姜玉莹1,鞠欣达2,杨丽娟1,吴典泽2,董志恒2()   

  1. 1.北华大学基础医学院生物化学与分子生物学教研室,吉林 吉林 132013
    2.北华大学基础医学院 病理学教研室,吉林 吉林 132013
  • 收稿日期:2025-11-06 接受日期:2025-12-31 出版日期:2026-09-28 发布日期:2026-10-15
  • 通讯作者: 董志恒 E-mail:2754855687@qq.com
  • 作者简介:曲 萌(1971-),女,吉林省吉林市人,副教授,医学博士,主要从事糖尿病慢性并发症方面的研究。
  • 基金资助:
    吉林省科技厅科技发展计划项目(YDZJ202301ZYTS106);吉林省科技厅科技发展计划项目(YDZJ202501ZYTS243);吉林省卫健委卫生健康科技能力提升项目(2022JC026);吉林省教育厅大学生创新训练项目(S202410201116)

Improvement effect of ginsenoside Rg3 on high glucose-induced injury in human renal tubular epithelial cells HK2 and its mechanism

Meng QU1,Tingxuan ZHANG1,Yuying JIANG1,Xinda JU2,Lijuan YANG1,Dianze WU2,Zhiheng DONG2()   

  1. 1.Department of Biochemistry and Molecular Biology,School of Basic Medicine,Beihua University,Jilin 132013,China
    2.Department of Pathology,School of Basic Medicine,Beihua University,Jilin 132013,China
  • Received:2025-11-06 Accepted:2025-12-31 Online:2026-09-28 Published:2026-10-15
  • Contact: Zhiheng DONG E-mail:2754855687@qq.com

摘要:

目的 探讨人参皂苷Rg3(G-Rg3)对高糖诱导人肾小管上皮细胞HK2损伤的改善作用,并阐明相关作用机制。 方法 采用高糖(HG)培养基(含25 mmol·L-1葡萄糖)诱导的人肾小管上皮细胞HK2损伤模型,将细胞分为阴性对照(NC)组(含5.5 mmol·L-1葡萄糖培养基)、HG组(HG培养基)、核因子E2相关因子2(Nrf2)抑制剂ML385组(ML385组)(HG培养基+5 μmol·L-1 ML385)、G-Rg3干预组(Rg3组)(HG培养基+40 μmol·L-1 G-Rg3)和ML385+Rg3组(HG培养基+5 μmol·L-1 ML385+40 μmol·L-1 G-Rg3)。采用细胞计数试剂盒8(CCK-8)法检测各组HK2细胞活性,2',7'-二氯二氢荧光素二乙酸酯(DCFH-DA)荧光法检测各组HK2细胞中活性氧(ROS)水平,试剂盒法检测各组HK2细胞中超氧化物歧化酶(SOD)和乳酸脱氢酶(LDH)活性以及丙二醛(MDA)和二价铁离子(Fe2?)水平,Western blotting法检测各组细胞中Nrf2、血红素加氧酶1(HO-1)、谷胱甘肽过氧化物酶4(GPX4)和长链酯酰辅酶A合成酶4(ACSL4)蛋白表达水平。 结果 CCK-8法、DCFH-DA荧光法和试剂盒法,培养48 h时,与NC组比较,HG组HK2细胞活性明显降低(P<0.01),细胞中ROS水平、LDH活性以及MDA和Fe2?水平均明显升高(P<0.01),SOD活性明显降低(P<0.01);与HG组比较,ML385组HK2细胞中ROS水平、LDH活性以及MDA和Fe2?水平均明显升高(P<0.05),SOD活性明显降低(P<0.05);Rg3组HK2细胞活性明显升高(P<0.01),细胞中ROS水平、LDH活性以及MDA和Fe2?水平均明显降低(P<0.01),SOD活性明显升高(P<0.01);与Rg3组比较,ML385+Rg3组HK2细胞活性明显降低(P<0.01),细胞中ROS水平、LDH活性以及MDA和Fe2?水平均明显升高(P<0.01),SOD活性明显降低(P<0.01)。Western blotting法,与NC组比较,HG组HK2细胞中Nrf2、HO-1和GPX4蛋白表达水平明显降低(P<0.01),ACSL4蛋白表达水平明显升高(P<0.01)。与HG组比较,ML385组HK2细胞中GPX4蛋白表达水平明显降低(P<0.01),ACSL4蛋白表达水平明显升高(P<0.01);Rg3组HK2细胞中Nrf2、HO-1和GPX4蛋白表达水平明显升高(P<0.01),ACSL4蛋白表达水平明显降低(P<0.05)。与Rg3组比较,ML385+Rg3组细胞中Nrf2、HO-1和GPX4蛋白表达水平明显降低(P<0.01),ACSL4蛋白表达水平明显升高(P<0.05)。 结论 G-Rg3对HG诱导的人肾小管上皮细胞HK2氧化损伤具有改善作用,其机制可能与上调Nrf2表达、激活Nrf2/HO-1/GPX4信号通路和抑制铁死亡有关。

关键词: 人参皂苷Rg3, 肾小管上皮细胞, 高糖环境, 铁死亡, Nrf2信号通路

Abstract:

Objective To investigate the improvement effect of ginsenoside Rg3 (G-Rg3) on high glucose-induced injury in human renal tubular epithelial HK2 cells, and to elucidate its mechanism. Methods A high glucose-induced injury model of human renal tubular epithelial HK2 cells was established using high glucose(HG) medium (containing 25 mmol·L-1 glucose). Cells were divided into negative control (NC) group (medium containing 5.5 mmol·L-1 glucose), HG group (HG medium), nuclear factor erythroid 2-related factor 2 (Nrf2) inhibitor ML385 group (ML385 group) (HG medium+5 μmol·L-1 ML385), G-Rg3 intervention group (Rg3 group) (HG medium+40 μmol·L-1 G-Rg3), and ML385+Rg3 group (HG medium + 5 μmol·L-1 ML385 + 40 μmol·L-1 G-Rg3). Cell counting kit-8 (CCK-8) method was used to detect the cell activities in cells in various groups. 2',7'-dichlorodihydrofluorescein diacetate(DCFH-DA) fluorescence method was used to detect the levels of reactive oxygen species (ROS) in the cells in various groups. Commercial kits were used to detect the activities of superoxide dismutase (SOD) and lactate dehydrogenase (LDH) and the levels of malondialdehyde (MDA) and ferrous ion(Fe2+) in the cells in various groups. Western blotting method was used to detect the expression levels of Nrf2, heme oxygenase-1 (HO-1), glutathione peroxidase 4 (GPX4), and acyl-CoA synthetase long-chain family member 4 (ACSL4) proteins in the cells in various groups. Results The results of CCK-8 method, DCFH-DA fluorescence method and kit method showed that, after 48 h of culture, compared with NC group, the cell activity was significantly decreased in HG group (P<0.01),the level of ROS, the activity of LDH, and the levels of MDA and Fe2+ in the cells were significantly increased (P<0.01), and the activity of SOD was significantly decreased (P<0.01). Compared with HG group, the level of ROS, the activity of LDH, and the levels of MDA and Fe2+ in the cells in ML385 group were significantly increased (P<0.05), and the activity of SOD was significantly decreased (P<0.05); the cell activity in Rg3 group was significantly increased (P<0.01), the level of ROS, the activity of LDH, and the levels of MDA and Fe2+ in the cells were significantly decreased (P<0.01), and the activity of SOD was significantly increased (P<0.01). Compared with Rg3 group, the cell activity in ML385+Rg3 group was significantly decreased (P<0.01), the level of ROS, the activity of LDH, and the levels of MDA and Fe2+ in the cells were significantly increased (P<0.01), and the activity of SOD was significantly decreased (P<0.01). The results of Western blotting method showed that, compared with NC group, the expression levels of Nrf2, HO-1, and GPX4 proteins in HK2 cells were significantly decreased in HG group (P<0.01), and the expression level of ACSL4 protein was significantly increased (P<0.01). Compared with HG group, the expression level of GPX4 protein in the cells in ML385 group was significantly decreased (P<0.01), and the expression level of ACSL4 protein was significantly increased (P<0.01); the expression levels of Nrf2, HO-1, and GPX4 proteins in HK2 cells were significantly increased in Rg3 group (P<0.01), and the expression level of ACSL4 protein was significantly decreased (P<0.05). Compared with Rg3 group, the expression levels of Nrf2, HO-1, and GPX4 proteins in HK2 cells in ML385+Rg3 group were significantly decreased (P<0.01), and the expression level of ACSL4 protein was significantly increased (P<0.05). Conclusion ?G-Rg3 showed an ameliorative effect on HG-induced oxidative injury in human renal tubular epithelial cells, and its mechanism may be associated with upregulating Nrf2 expression, activating the Nrf2/HO-1/GPX4 signaling pathway, and inhibiting ferroptosis.

Key words: Ginsenoside Rg3, Renal tubular epithelial cell, High-glucose environment, Ferroptosis, Nrf2 signaling pathway

中图分类号: 

  • R285.5