Isoacteoside attenuates acute kidney injury induced by severe acute pancreatitis

被引:13
|
作者
Wang, Bin [1 ,2 ]
Li, Xi-Han [3 ]
Song, Zhang [3 ]
Li, Min-Li [2 ]
Wu, Xiao-Wei [2 ]
Guo, Mei-Xia [2 ]
Zhang, Xiao-Hua [2 ]
Zou, Xiao-Ping [3 ]
机构
[1] Nanjing Univ Chinese Med, Nanjing Drum Tower Hosp, Clin Coll, Nanjing 210008, Jiangsu, Peoples R China
[2] Jinling Hosp, Dept Gastroenterol, Nanjing 210002, Jiangsu, Peoples R China
[3] Nanjing Univ, Affiliated Hosp, Nanjing Drum Tower Hosp, Dept Gastroenterol, 321 Zhongshan Rd, Nanjing 210008, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
severe acute pancreatitis; acute kidney injury; Isoacteoside; TLR4; NF-κ B;
D O I
10.3892/mmr.2021.11926
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Severe acute pancreatitis (SAP) is a common acute abdominal disease accompanied by systemic inflammatory response syndrome, which may be complicated by acute kidney injury (AKI). Isoacteoside (ISO) is the active ingredient of Monochasma savatieri Franch. ex Maxim and has been reported to have anti-inflammatory activities. The present study detected the effects of ISO on AKI induced by SAP in rat models, and the underlying mechanism. The optimum dose of ISO for treatment of AKI induced by SAP was determined. The serum levels of TNF-alpha and IL-6 were estimated using an ELISA. Kidney injury was evaluated by histopathological examination, and the expression levels of nitric oxide were also detected. The expression levels of Toll-like receptor 4 (TLR4) and NF-kappa B p65 were measured by immunohistochemistry and western blotting. The results revealed that ISO may serve a critical role in ameliorating AKI induced by SAP. These effects may be associated with the TLR4/NF-kappa B signaling pathway.
引用
收藏
页数:10
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