Synthesis of glycyrrhizin analogues as HMGB1 inhibitors and their activity against sepsis in acute kidney injury

被引:3
|
作者
Qiang, Xin [1 ]
Peng, Yijie [1 ]
Wang, Zongyuan [1 ]
Fu, Wenjie [1 ]
Li, Wei [1 ]
Zhao, Quanyi [1 ]
He, Dian [1 ]
机构
[1] Lanzhou Univ, Sch Pharm, Inst Med Chem, Mat Med Dev Grp, Lanzhou 730000, Peoples R China
关键词
Glycyrrhizin analogues; C-N glycoside bond; HMGB1; Kidney injury; NF-KAPPA-B; 18-BETA-GLYCYRRHETINIC ACID; INFLAMMATORY RESPONSE; BIOLOGICAL EVALUATION; SUPPRESSION; DERIVATIVES; CELLS; AKI;
D O I
10.1016/j.ejmech.2023.115696
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glycyrrhizin (GL) is one of the antagonists of highly conserved nuclear protein (HMGB1). The researches have shown that the glycosyl of GL is an important pharmacophore for GL binding to HMGB1, and it is the determinant factor for mechanism of action. To get the HMGB1 inhibitors with higher activity and good pharmaco-kinetic properties, two classes of GL analogues containing C-N glycoside bond were synthesized, and their antiinflammatory, anti-oxidative stress and anti-septic kidney injury were evaluated. The results are as follows. First, in the anti-inflammatory assay, all the compounds inhibited NO release in some degree; among them, compound 6 displayed the strongest NO inhibitory effect with IC50 value of 15.9 mu M, and compound 15 with IC50 of 20.2 mu M. The two compounds not only decreased IL-1 ss and TNF- a levels in RAW264.7 cells and HK-2 cells, but also downregulated the levels of NLRP3, P-NF-kappa B p65 and HMGB1 in activated HK-2 cells in a dose-dependent manner. Second, in the renal protection assay with H2O2-stimulated HK-2 cell line, they reduced MDA level and increased SOD in HK-2 cells; additionally, they also inhibited the HK-2 cell apoptosis and downregulated the Caspase-1 p20 level. Third, in the in vivo activity tests of the septic mouse, they also showed good activities just like in vitro, decreasing the IL-1 ss, TNF-alpha, MDA, blood creatinine (Scr) and urea nitrogen (BUN) in serum, and increasing SOD levels in a dose-dependent manner. The immunoblotting results showed the two compounds downregulated the levels of HMGB1, P-NF-kappa B p65, NLRP3 and Caspase-1 p20 protein. All in all, the two compounds improved the renal injury of septic mice, and alleviated the tube wall structure damage and renal tubular dilation in kidney, which further proved by H&E staining. This suggests the two compounds have septic acute kidney injury activity, and they will be potential therapeutic drugs for septic acute kidney injury.
引用
收藏
页数:19
相关论文
共 50 条
  • [11] Quercetin improves contrast-induced acute kidney injury through the HIF-1α/lncRNA NEAT1/HMGB1 pathway
    Luo, Min
    Liu, Ziyu
    Hu, Zongren
    He, Qinghu
    PHARMACEUTICAL BIOLOGY, 2022, 60 (01) : 889 - 898
  • [12] HMGB1 and LPS induce distinct patterns of gene expression and activation in neutrophils from patients with sepsis-induced acute lung injury
    Silva, Eliezer
    Arcaroli, John
    He, Qianbin
    Svetkauskaite, Daiva
    Coldren, Christopher
    Nick, Jerry A.
    Poch, Katie
    Park, Jong Sung
    Banerjee, Anirban
    Abraham, Edward
    INTENSIVE CARE MEDICINE, 2007, 33 (10) : 1829 - 1839
  • [13] MicroRNA-181b Inhibits Inflammatory Response and Reduces Myocardial Injury in Sepsis by Downregulating HMGB1
    Lan Ling
    Lida Zhi
    Haifeng Wang
    Yihuan Deng
    Chengdong Gu
    Inflammation, 2021, 44 : 1263 - 1273
  • [14] MicroRNA-181b Inhibits Inflammatory Response and Reduces Myocardial Injury in Sepsis by Downregulating HMGB1
    Ling, Lan
    Zhi, Lida
    Wang, Haifeng
    Deng, Yihuan
    Gu, Chengdong
    INFLAMMATION, 2021, 44 (04) : 1263 - 1273
  • [15] Sodium butyrate alleviates LPS-induced acute lung injury in mice via inhibiting HMGB1 release
    Li, Na
    Liu, Xin-xin
    Hong, Mei
    Huang, Xin-zhou
    Chen, Hui
    Xu, Jia-huan
    Wang, Chao
    Zhang, Yan-xiang
    Zhong, Ji-xin
    Nie, Hao
    Gong, Quan
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2018, 56 : 242 - 248
  • [16] Use of kidney injury molecule-1 for sepsis-associated acute kidney injury staging
    Molinari, Luca
    Landsittel, Douglas P.
    Kellum, John A.
    ProCESS Investigator
    ProGReSS-AKI Investigator
    NEPHROLOGY DIALYSIS TRANSPLANTATION, 2023, 38 (06) : 1560 - 1563
  • [17] High-Mobility Group Box 1 (HMGB1) and Autophagy in Acute Lung Injury (ALI): A Review
    Qu, Lihua
    Chen, Chao
    Chen, YangYe
    Li, Yi
    Tang, Fang
    Huang, Hao
    He, Wei
    Zhang, Ran
    Shen, Li
    MEDICAL SCIENCE MONITOR, 2019, 25 : 1828 - 1837
  • [18] Activation ADORA1 protects against sepsis-associated acute kidney injury by inhibiting pyroptosis
    He, Wei
    Pan, Kaixin
    Xiao, Chenggen
    TISSUE & CELL, 2025, 95
  • [19] Allylpyrocatechol ameliorates sepsis-induced lung injury via SIRT1-mediated suppression of p65 and nucleocytoplasmic translocation of HMGB1
    Mu, Yanfei
    Mu, Xiaosong
    Yang, Yan
    Zhou, Yanhong
    MOLECULAR & CELLULAR TOXICOLOGY, 2021, 17 (04) : 397 - 407
  • [20] Lycorine attenuates lipopolysaccharide-induced acute lung injury through the HMGB1/TLRs/NF-κB pathway
    Ge, Xin
    Meng, Xianglin
    Fei, Dongsheng
    Kang, Kai
    Wang, Qiubo
    Zhao, Mingyan
    3 BIOTECH, 2020, 10 (08)