Carnosic acid nanoparticles suppress liver ischemia/reperfusion injury by inhibition of ROS, Caspases and NF-κB signaling pathway in mice

被引:45
|
作者
Li, Hui [1 ]
Sun, Jian-Jun [2 ]
Chen, Guo-Yong [2 ]
Wang, Wei-Wei [2 ]
Xie, Zhan-Tao [2 ]
Tang, Gao-Feng [2 ]
Wei, Si-Dong [2 ]
机构
[1] Zhengzhou Univ, Henan Prov Peoples Hosp, Dept Intervent Radiol, 7 Weiwu Rd, Zhengzhou 450003, Henan, Peoples R China
[2] Zhengzhou Univ, Henan Prov Peoples Hosp, Dept Liver Gallbladder Pancreas Surg, 7 Weiwu Rd, Zhengzhou 450003, Henan, Peoples R China
关键词
Ischemia/reperfusion injury; Carnosic acid nanoparticles; ROS; Apoptosis; Inflammation; THIOREDOXIN-INTERACTING-PROTEIN; CELLS; ACTIVATION; APOPTOSIS; TRANSPLANTATION; EXPRESSION; INDUCTION; FIBROSIS; RATS;
D O I
10.1016/j.biopha.2016.04.064
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Living donor liver transplantation (LDLT) requires ischemia/reperfusion (I/R), which can lead to early graft injury. However, the detailed molecular mechanism of I/R injury remains unclear. Carnosic acid, as a phenolic diterpene with function of anti-inflammation, anti-cancer, anti-bacterial, anti-diabetic, as well as neuroprotective properties, is produced by many species from Lamiaceae family. Nanoparticulate drug delivery systems have been known to better the bioavailability of drugs on intranasal administration compared with only drug solutions. Administration of carnosic acid nanoparticles was thought to be sufficient to lead to considerable inhibition of liver injury progression induced by ischemia/reperfusion. In our study, liver ischemia/reperfusion injury was established successfully with C57BL/6 animal model. 10 and 20 mg/kg carnosic acid nanoparticles were injected to mice for five days prior to ischemia. After liver ischemia/reperfusion, the levels of serum AST, ALT and APL were increased, which was attenuated by pre-treatment with carnosic acid nanoparticles. In addition, carnosic acid nanoparticles inhibited ROS production via its related signals regulation. And carnosic acid nanoparticles also suppressed the ischemia/reperfusion-induced up-regulation in the pro-apoptotic protein and mRNA levels of Bax, Cytoc, Apaf-1 and Caspase-9/3 while increased ischemia/reperfusion-induced decrease of anti-apoptotic factor of Bcl-2. Further, ischemia/reperfusion-induced inflammation was also inhibited for carnosic acid nanoparticles administration via inactivating NF-kappa B signaling pathway, leading to down-regulation of pro-inflammatory cytokines releasing. In conclusion, our study suggested that carnosic acid nanoparticles protected against liver ischemia/reperfusion injury via its role of anti-oxidative, anti-apoptotic and anti-inflammatory bioactivity. (C) 2016 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:237 / 246
页数:10
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