基础医学与临床 ›› 2026, Vol. 46 ›› Issue (3): 367-373.doi: 10.16352/j.issn.1001-6325.2026.03.0367

• 研究论文 • 上一篇    下一篇

大株红景天注射液对非酒精性脂肪性肝病模型大鼠的治疗作用

徐霞1, 王富兵1, 赵培培2, 范辉1, 李欣1, 张谷3, 顾新红1*   

  1. 南通市第二人民医院(南通大学附属康复医院) 1.消化内科;2.老年科, 江苏 南通 226002;
    3.浙江省肿瘤医院 病理科,浙江 杭州 310005
  • 收稿日期:2025-03-14 修回日期:2025-06-23 出版日期:2026-03-05 发布日期:2026-02-25
  • 通讯作者: *1562416434@qq.com
  • 基金资助:
    南通市基础科学研究和社会民生科技计划项目(MSZ2022135)

Therapeutic effects of Sofren injection on non-alcoholic fatty liver disease in rat models

XU Xia1, WANG Fubing1, ZHAO Peipei2, FAN Hui1, LI Xin1, ZHANG Gu3, GU Xinhong1*   

  1. 1. Department of Gastroenterology, 2. Department of Geriatrics, Nantong Second People′s Hospital(Rehabilitation Hospital Affiliated to Nantong University), Nantong 226002;
    3. Department of Pathology, Zhejiang Cancer Hospital, Hangzhou 310005, China
  • Received:2025-03-14 Revised:2025-06-23 Online:2026-03-05 Published:2026-02-25
  • Contact: *1562416434@qq.com

摘要: 目的 探讨大株红景天(Sofren)注射液对非酒精性脂肪性肝病(NAFLD)模型大鼠肝损伤的干预效果。方法 将实验大鼠随机分为对照组、NAFLD模型组及Sofren治疗组。模型组与Sofren注射液治疗组予以高脂饲料喂养8周以诱导NAFLD。造模成功后,Sofren注射液治疗组经尾静脉给予Sofren注射液(0.4 mL/100 g),持续干预8周。实验结束后,检测血清肝功能指标丙氨酸氨基转移酶(ALT)与天冬氨酸氨基转移酶(AST),炎性介质TNF-α、IL-1β、IL-6、MDA水平以及血清SOD活性。肝组织行苏木精-伊红(HE)与普鲁士蓝染色观察病理变化与铁沉积。采用免疫组化与Western blot检测肝组织内核因子E2相关因子2(Nrf2)、血红素加氧酶-1(HO-1)、谷胱甘肽过氧化物酶4(GPX4)、转铁蛋白受体1(TFR1)及铁蛋白重链1(FTH1)的蛋白表达。结果 相较于对照组,模型组大鼠表现出显著的肝损伤,血清ALT、AST、MDA及炎性因子(TNF-α、IL-1β、IL-6)水平显著升高,SOD活性降低,肝脏铁沉积增加。同时,肝组织Nrf2、HO-1及GPX4蛋白表达下调,而TFR1与FTH1表达上调(P<0.05)。经Sofren注射液干预后,上述异常指标均得到显著改善(P<0.05)。结论 Sofren注射液能够改善NAFLD大鼠的肝损伤。

关键词: 大株红景天注射液, 非酒精性脂肪性肝病, 核因子E2相关因子2, 血红素加氧酶-1, 铁死亡

Abstract: Objective To investigate the hepato-protective effects of Sorfren injection on rat liver injury resulted from non-alcoholic fatty liver disease (NAFLD). Methods Rats were randomly divided into control, NAFLD model and Sofren-treated groups. The Sofren-treated groups was developed by feeding a high-fat diet (HFD) for 8 weeks. Subsequently, the Sofren-treated group received tail vein injections of Sofren solution (0.4 mL/100 g) for 8 weeks. Serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels were measured using an automatic biochemical analyzer. Tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β),IL-6 and malondialdehyde (MDA) were quantified by enzyme-linkedimmunosorbent assay(ELISA). Superoxide dismutase (SOD) activity was assessed by chromogenic method. Histopathological evaluations were performed by Hematoxylin-Eosin (HE) and Prussian blue staining. Immunohistochemistry and Western blot were applied to analyze the expression of glutathione peroxidase 4 (GPX4), nuclear factor erythroid 2-related factor 2 (Nrf2),heme oxygenase-1 (HO-1), transferrin receptor 1 (TFR1) and ferritin heavy chain 1 (FTH1). Results Compared with control group, the model group exhibited significant elevation of serum ALT, AST, MDA, and inflammatory mediators (TNF-α, IL-1β, IL-6), reduction of SOD activity, increased hepatic iron deposition, down-regulated Nrf2, HO-1, and GPX4 expression, and up-regulated level of TFR1 and FTH1(P<0.05). Treatment with Sofren injection markedly reversed these pathological alterations(P<0.05). Conclusions Sofren injection may alleviate liver injury in NAFLD rats.

Key words: Sofren injection, non-alcoholic fatty liver disease, nuclear factor erythroid 2-related factor 2, heme oxygenase-1, ferroptosis

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