华中科技大学学报(医学版) ›› 2026, Vol. 55 ›› Issue (4): 483-489.doi: 10.3870/j.issn.1672-0741.25.08.004

• 论著 • 上一篇    下一篇

姜黄素通过PI3K/Akt/mTOR信号通路改善小鼠系统性红斑狼疮*

陈杰1, 刘路2△, 胡蜜2, 颜苏艳3, 王优1, 罗丹1   

  1. 武汉市第三医院 1肾内风湿免疫科 3内科,武汉 430060
    武汉市第三医院光谷院区 2儿科,武汉 430070
  • 收稿日期:2025-07-29 出版日期:2026-08-15 发布日期:2026-07-28
  • 通讯作者: E-mail:370382567@qq.com
  • 作者简介:陈 杰,男,1982年生,医学硕士,主治医师,E-mail:cjghvhj@163.com
  • 基金资助:
    *武汉市卫生健康委员会资助项目(No.WX19Z38)

Curcumin Improves Systemic Lupus Erythematosus in Mice Through PI3K/Akt/mTOR Signaling Pathway

Chen Jie1, Liu Lu2△, Hu Mi2, et al   

  1. 1Department of Nephrology and Rheumatology,Wuhan Third Hospital,Wuhan 430060,China
    2Department of Pediatrics,Wuhan Third Hospital,Guanggu Branch,Wuhan 430070,China
  • Received:2025-07-29 Online:2026-08-15 Published:2026-07-28
  • Contact: E-mail:370382567@qq.com

摘要: 目的 探讨姜黄素对小鼠系统性红斑狼疮(SLE)的改善作用,并分析其作用机制。方法 10只MRL/MpJ小鼠作为对照组,40只MRL/lpr小鼠随机分为模型组、低剂量组、高剂量组和联合组,每组各10只,低剂量组、高剂量组分别灌胃250 mg/kg、500 mg/kg的姜黄素,联合组灌胃500 mg/kg的姜黄素并尾静脉注射20 mg/kg磷脂酰肌醇-3-激酶(PI3K)激动剂740 Y-P。各组均连续干预8周后检测24 h尿蛋白、血清肌酐(Scr)、尿素氮(BUN),ELISA法检测血清炎症因子[白介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)、γ-干扰素(IFN-γ)]水平及自身抗体[抗小核糖核蛋白(snRNP/Sm)抗体、抗双链DNA(dsDNA)抗体]水平;苏木精-伊红(HE)染色观察肾组织病理形态学变化;免疫荧光法检测免疫复合物和补体沉积情况;Western blot法检测CD4、CD19、CD20、PI3K、磷酸化PI3K(p-PI3K)、蛋白激酶B(Akt)、磷酸化Akt(p-Akt)、哺乳动物雷帕霉素靶蛋白(mTOR)及磷酸化mTOR(p-mTOR)蛋白表达情况。结果 与对照组相比,模型组小鼠24 h尿蛋白、血清Scr和BUN水平、血清炎症因子(IL-6、TNF-α、IFN-γ)水平、自身抗体(Anti-dsDNA、Anti-snRNP)水平、肾组织IgG和C3沉积水平以及CD4、CD19、CD20和p-PI3K、p-Akt及p-mTOR蛋白表达均显著升高(均P<0.05)。低、高剂量组上述指标较模型组均显著降低,且高剂量组效果更显著(均P<0.05);联合组上述指标高于高剂量组(均P<0.05)。HE染色显示,低、高剂量组小鼠肾组织病理病变明显改善,高剂量组更优,联合组肾组织损伤较高剂量组严重。结论 姜黄素可改善SLE小鼠免疫紊乱和肾损伤,可能通过PI3K/Akt/mTOR信号通路发挥作用。

关键词: 姜黄素, 系统性红斑狼疮, 免疫紊乱, 肾损伤, 磷脂酰肌醇-3-激酶, 蛋白激酶B, 哺乳动物雷帕霉素靶蛋白

Abstract: Objective To explore the improvement effect of curcumin on systemic lupus erythematosus(SLE)in mice and analyze its mechanism.Methods Ten MRL/MpJ mice were used as the control group,while 40 MRL/lpr mice were randomly divided into four groups:the model group,the low-dose group,the high-dose group,and the combination group,with 10 mice in each group.The low-dose and high-dose groups were administered curcumin at doses of 250 mg/kg and 500 mg/kg,respectively,via oral gavage.The combination group received 500 mg/kg of curcumin via oral gavage along with an intravenous injection of 20 mg/kg of the phosphatidylinositol-3-kinase(PI3K)activator 740Y-P.After 8 weeks of continuous intervention,24-hour urinary protein,serum creatinine(Scr),and blood urea nitrogen(BUN)levels were measured.Serum levels of inflammatory factors[interleukin-6(IL-6),tumor necrosis factor-α(TNF-α),and interferon-γ(IFN-γ)]and autoantibodies[anti-small nuclear ribonucleoprotein(snRNP/Sm)and anti-doublestranded DNA(dsDNA)antibodies]were detected by using ELISA.Renal histopathological changes were observed by hematoxylin-eosin(HE)staining.Immunofluorescence was used to detect immune complex and complement deposition.Western blot was performed to assess the expression levels of CD4,CD19,CD20,PI3K,phosphorylated PI3K(p-PI3K),protein kinase B(Akt),phosphorylated Akt(p-Akt),mammalian target of rapamycin(mTOR),and phosphorylated mTOR(p-mTOR).Results Compared with the control group,the 24-hour urine protein,serum Scr and BUN levels,serum inflammatory factors(IL-6,TNF-α,IFN-γ),autoantibodies(anti-dsDNA,anti-snRNP/Sm),renal IgG and C3 deposition levels,and CD4,CD19,CD20,p-PI3K,p-Akt,p-mTOR protein expressions in the model group were significantly increased(all P<0.05).The above indicators in low and high dose groups were significantly lower,and the effect was more significant in the high-dose group.The indexs were significantly lower than that in the model group,and the effect in the high-dose group was more significant(all P<0.05).The above indexes in the combined group were higher than those in the high dose group(P<0.05).HE staining showed that the pathological changes of renal tissue in low and high dose groups were obviously improved,especially in high dose group,and the damage of renal tissue in combined group was more serious than that in high dose group.Conclusion Curcumin can ameliorate immune dysregulation and renal injury in SLE mice,potentially through the regulation of the PI3K/Akt/mTOR signaling pathway.

Key words: curcumin, systemic lupus erythematosus, immune dysregulation, renal injury, phosphatidylinositol-3-kinase, protein kinase B, mammalian target of rapamycin

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