南方医科大学学报 ›› 2025, Vol. 45 ›› Issue (9): 1938-1945.doi: 10.12122/j.issn.1673-4254.2025.09.13

• • 上一篇    

鬼箭羽通过抑制AGEs-RAGE信号转导通路改善晚期糖基化终末产物诱导的小鼠肾足细胞损伤

马倩倩1(), 牛钰琪2, 左铭钰1, 李鑫1, 符竣轲1, 王瑾瑾2()   

  1. 1.河南中医药大学,中医(仲景)学院,河南 郑州 450046
    2.河南中医药大学,医学院,河南 郑州 450046
  • 收稿日期:2025-02-13 出版日期:2025-09-20 发布日期:2025-09-28
  • 通讯作者: 王瑾瑾 E-mail:wtt01232024@163.com;wangjinjin@hactcm.edu.cn
  • 作者简介:马倩倩,在读硕士研究生,E-mail: wtt01232024@163.com
  • 基金资助:
    国家自然科学基金(82104748)

Guijianyu alleviates advanced glycation endproducts-induced mouse renal podocyte injury by inhibiting the AGEs-RAGE signaling pathway

Qianqian MA1(), Yuqi NIU2, Mingyu ZUO1, Xin LI1, Junke FU1, Jinjin WANG2()   

  1. 1.Traditional Chinese Medicine (Zhongjing) School, Henan University of Chinese Medicine, Zhengzhou 450046, China
    2.School of Medicine, Henan University of Chinese Medicine, Zhengzhou 450046, China
  • Received:2025-02-13 Online:2025-09-20 Published:2025-09-28
  • Contact: Jinjin WANG E-mail:wtt01232024@163.com;wangjinjin@hactcm.edu.cn
  • Supported by:
    National Natural Science Foundation of China(82104748)

摘要:

目的 观察鬼箭羽对晚期糖基化终末产物(AGEs)刺激的小鼠肾足细胞(MPC-5)AGEs-晚期糖基化终末产物受体(RAGE)信号转导通路及下游靶点的影响,并阐明鬼箭羽改善糖尿病肾脏疾病(DKD)足细胞损伤的机制。 方法 鬼箭羽干预糖尿病肾脏疾病动物模型,利用透射电镜观察肾脏形态与结构;实时荧光定量-聚合酶链反应(RT-qPCR)、免疫组化检测相关基因与核心蛋白的表达情况。体外培养MPC-5,采用浓度为50 mg/L糖基化终末期产物-牛血清白蛋白(AGEs-BSA)培养液孵育24 h,诱导建立糖尿病细胞模型。利用CCK-8法检测技术,评价造模后的细胞成活率。将对数生长期的MPC-5随机分为正常组、模型组、鬼箭羽组、RAGE激动剂(D-Ribose)组、鬼箭羽+RAGE激动剂(D-Ribose)组,利用CCK-8法筛选不同浓度鬼箭羽对MPC-5细胞活力的影响。蛋白免疫印迹法检测各组细胞RAGE、VEGFA、TNF-α、NF-κB(p65)、IL-6、Caspase-3蛋白表达;RT-qPCR检测RAGE、NF-κB(p65)、VEGFA、IL-6mRNA表达。 结果 体内结果表明,鬼箭羽干预后,与模型组相比,干预组动物模型肾脏组织足细胞病理变化有所改善。免疫组化结果显示,与模型组比较,鬼箭羽高剂量组RAGE、VEGFA、NF-κB(p65)、IL-6蛋白表达降低(P<0.05);RT-qPCR结果显示,与模型组比较,鬼箭羽高剂量组RAGE、NF-κB、IL-6mRNA表达降低(P<0.05)。体外结果表明,与正常组相比,模型组细胞活力显著降低(P<0.05),RAGE、NF-κB(p65)、VEGFA、TNF-α、IL-6和Caspase-3蛋白表达升高(P<0.05),RAGE、NF-κB(p65)、VEGFA和IL-6 mRNA表达升高(P<0.05);与模型组比较,浓度为550 mg/L的鬼箭羽干预成模后的MPC-5,24 h提高细胞活力最为显著(P<0.05),降低RAGE、NF-κB(p65)、VEGFA、TNF-α、IL-6和Caspase-3蛋白表达(P<0.05);而鬼箭羽+RAGE激动剂可逆转RAGE激动剂对MPC-5模型中RAGE、VEGFA、TNF-α、IL-6和Caspase-3蛋白表达的改变(P<0.05),同时与RAGE激动剂组比较,鬼箭羽+RAGE激动剂组RAGE、NF-κB(p65)、IL-6、VEGFAmRNA表达显著降低(P<0.01)。 结论 鬼箭羽可以通过抑制AGEs-RAGE信号转导通路的激活,减少下游促炎细胞因子和血管内皮生长因子的表达,进而发挥改善AGEs诱导糖尿病肾脏疾病MPC-5损伤的作用。

关键词: 鬼箭羽, 糖尿病肾脏疾病, 足细胞, AGEs-RAGE信号通路, 晚期糖基化终末产物

Abstract:

Objective To investigate the mechanism by which Guijianyu ameliorates podocyte injury in a mouse model of diabetic kidney disease (DKD) induced by advanced glycation endproducts (AGEs). Methods Sixty db/db mouse models of DKD were randomized equally into 5 groups for treatment with saline, Guijianyu extract at 3 doses or irbesartan for 12 weeks, and the changes in renal pathology and structure were observed using transmission electron microscopy, and the expressions of related genes and key proteins were detected using RT-qPCR and immunohistochemistry. In cultured MPC-5 cells incubated with 50 mg/L AGEs-BSA for 24 h, the effect of different concentrations of Guijianyu extract on cell viability was examined with CCK-8 assay; Western blotting was performed to detect the protein expressions of RAGE, VEGFA, TNF-α, NF-κB(p65), IL-6 and caspase-3, and the mRNA expressions of RAGE, NF-κB (p65), VEGFA and IL-6 were detected with RT-qPCR. Results In mouse models of DKD, treatment with high-dose Guijianyu extract significantly reduced renal expressions of RAGE, VEGFA, NF-κB(p65), and IL-6 proteins and the mRNA expressions of RAGE, NF-κB, and IL-6. In MPC-5 cells, exposure to AGEs significantly reduced cell viability and increased the protein expressions of RAGE, NF‑κB (p65), VEGFA, TNF-α, IL-6 and caspase-3 (P<0.05) and mRNA expressions of RAGE, NF-κB (p65), VEGFA, and IL-6. Treatment with Guijianyu extract obviously improved cell viability and reduced the expressions of RAGE, NF-κB(p65), VEGFA, TNF-α, IL-6, and caspase-3. Furthermore, Guijianyu extract effectively reversed RAGE agonist-induced elevation of protein expressions of RAGE, VEGFA, TNF-α, IL-6, and caspase-3 and mRNA expressions of RAGE, NF-κB (p65), IL-6, and VEGFA in MPC-5 cells. Conclusion Guijianyu extract ameliorates AGEs-induced mouse renal podocyte injury in DKD by inhibiting the activation of AGEs-RAGE signaling pathway and reducing the expressions of pro-inflammatory cytokines and vascular endothelial growth factors.

Key words: Guijianyu, diabetic kidney disease, podocytes, AGEs-RAGE signaling pathway, advanced glycation endproducts