Esculetin alleviates murine lupus nephritis by inhibiting complement activation and enhancing Nrf2 signaling pathway

被引:23
|
作者
Zhang, Ying [1 ]
Li, Zhaojun [2 ]
Wu, Haijie [2 ]
Wang, Jing [3 ]
Zhang, Sen [2 ]
机构
[1] Univ Sci & Technol Beijing, Univ Hosp, Dept Internal Med, Beijing 100083, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Mat Med, State Key Labboratory Bioact Subst & Funct Nat Med, Beijing 100050, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 1, Dept Radiotherapy, Beijing 100853, Peoples R China
基金
北京市自然科学基金;
关键词
Lupus nephritis; Esculetin; Complement activation; Molecular docking; Nrf2; Fibrosis; OXIDATIVE STRESS; MYCOPHENOLATE-MOFETIL; PROTECTS; KIDNEY; MICE; EXPRESSION; KEAP1-NRF2; IL-10; TH2; C3;
D O I
10.1016/j.jep.2022.115004
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Esculetin is a bioactive compound of medicinal herb Hydrangea paniculata, and has showed anti-oxidation and anti-inflammation bioactivities. Renal local oxidative stress and inflammation are import contributors for progression of lupus nephritis (LN). Aim of the study: In the present study, the renal protective effect of esculetin against LN was evaluated using MRL/lpr mice. Materials and methods: MRL/lpr mice were orally administrated with esculetin (20 mg/kg and 40 mg/kg) from 10 to 20 weeks and then renal function and kidney pathology were analyzed. Results: Esculetin significantly attenuated renal impairment in MRL/lpr mice by reducing blood urea nitrogen (BUN), serum creatinine (Scr) and albuminuria, and ameliorated the glomerular hypertrophy, tubular interstitial fibrosis and mononuclear cell infiltration into interstitium. mRNA microarray suggested that esculetin could significantly down-regulate complement cascade, inflammation and fibrosis pathway, and up-regulate Nrf2-related anti-oxidation genes. Most surprising finding in the current study was that esculetin could inhibit the complement activation both in classical and alternative pathway using in vitro hemolysis assay, further enzyme assay suggested that esculetin blocked the C3 convertase (C4b2a) to exert this inhibitory capability. Molecular docking predicted that esculetin had four conventional hydrogen bonds interacting with C4b2a, and CDOCKER energy is relatively lower. Luciferase reporter gene demonstrated that esculetin could activate Nrf2 signaling pathway, and further flow cytometry confirmed that anti-oxidation bioactivity of esculetin was dependent on Nrf2 activation. On the other hand, esculetin could inhibit NF kappa B nuclear translocation and TGF beta-smad3 pro-fibrosis pathway. Conclusion: Esculetin shows beneficial effect on LN progression, and it may be a good natural leading compound for design of chemical compounds to treat LN.
引用
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页数:13
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