Saikosaponin-D Prevents Acute Renal Injury via Inhibition of NLRP3 Inflammasome By SIRT1

被引:2
|
作者
Kang, Lin [1 ]
Yang, Fan [1 ]
Zhang, Xiuzhi [1 ]
Zhao, Jing [3 ]
Liu, Yang [1 ]
Zhao, Huanfen [1 ]
Hu, Zhijuan [2 ]
Liu, Bing [2 ]
He, Chunnian [1 ]
机构
[1] Hebei Gen Hosp, Dept Pathol, China 050051, Hebei, Peoples R China
[2] Hebei Gen Hosp, Dept Nephrol, Shijiazhuang 050051, Hebei, Peoples R China
[3] Hebei Gen Hosp, Dept Oncol, Shijiazhuang 050051, Hebei, Peoples R China
关键词
saikosaponin-d; acute renal injury; NLRP3; SIRT1; ACUTE KIDNEY INJURY; SUPPRESSION;
D O I
10.1007/s11094-022-02554-w
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The chemical composition of bupleurum plant is complex. The main active components of bupleurum are saponins, volatile oils, flavonoids and polysaccharides, exerting multiple pharmacological effects. Here, we have first found that saikosaponin-d (SSD) reduced kidney injury and inflammation, induced SIRT1, and suppressed protein expression on in vivo mice model of acute kidney injury (AKI). In LPS-induced kidney cell inflammation model, SSD suppressed IL-1B, NLRP3, SIRT1 and ROS expression as detected after cells were treated with SSD. Furthermore, the anti-inflammation effects of SSD on inflammation and kidney injury were detected on in vivo mice model of ARI via NLRP3 expression. The results showed that ROS inhibitor increased anti-inflammation effects of SSD on in vivo mice inflammation model and in vitro model. Finally, NLRP3 inhibitor also reduced anti-inflammation effects of SSD on in vivo mice inflammation model and in vitro model. On the whole, these findings confirm that SSD prevents AKI via inhibition of NLRP3 inflammasome by SIRT1.
引用
收藏
页码:1169 / 1176
页数:8
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