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
相关论文
共 50 条
  • [1] Baicalein pretreatment protects against liver ischemia/reperfusion injury via inhibition of NF-κB pathway in mice
    Liu, Anding
    Huang, Liang
    Fan, Hua
    Fang, Haoshu
    Yang, Yan
    Liu, Shenpei
    Hu, Jifa
    Hu, Qi
    Dirsch, Olaf
    Dahmen, Uta
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2015, 24 (01) : 72 - 79
  • [2] Daphnetin Protects against Cerebral Ischemia/Reperfusion Injury in Mice via Inhibition of TLR4/NF-κB Signaling Pathway
    Liu, Jia
    Chen, Qianxue
    Jian, Zhihong
    Xiong, Xiaoxing
    Shao, Lingmin
    Jin, Tong
    Zhu, Xiqun
    Wang, Lei
    BIOMED RESEARCH INTERNATIONAL, 2016, 2016
  • [3] Hydrogen gas inhalation protects against liver ischemia/reperfusion injury by activating the NF-κB signaling pathway
    Zhang, Chao-Bin
    Tang, Yi-Chen
    Xu, Xue-Jun
    Guo, Shi-Xiang
    Wang, Huai-Zhi
    EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2015, 9 (06) : 2114 - 2120
  • [4] Selective inactivation of NF-κB in the liver using NF-κB decoy suppresses hepatic ischemia/reperfusion injury in mice
    Suzumura, K.
    Hirano, T.
    Son, G.
    Limuro, Y.
    Iiboshi, Y.
    Oh, K.
    Satake, M.
    Fujimoto, J.
    JOURNAL OF HEPATOLOGY, 2008, 48 : S169 - S169
  • [5] Isosteviol plays a protective role on hepatic ischemia and reperfusion injury in mice through MAPK/NF-κB signaling pathway
    Chen, Yuwei
    Li, Ronghua
    Xu, Hongjiao
    Guo, Long
    TRANSLATIONAL GASTROENTEROLOGY AND HEPATOLOGY, 2024, 9
  • [6] Sevoflurane alleviates liver ischemia reperfusion injury through inactivation of the TRAF6/NF-ΚB signaling pathway
    Liu, Hongqiang
    Yuan, Ying
    Rao, Dan
    TROPICAL JOURNAL OF PHARMACEUTICAL RESEARCH, 2021, 20 (10) : 2043 - 2048
  • [7] Ephedrine attenuates cerebral ischemia/reperfusion injury in rats through NF-κB signaling pathway
    Shi, Chanhong
    Li, Jianhong
    Li, Jianwei
    HUMAN & EXPERIMENTAL TOXICOLOGY, 2021, 40 (06) : 994 - 1002
  • [8] Effects of NF-κB inhibition on mesenteric ischemia-reperfusion injury
    Zou, L
    Attuwaybi, B
    Kone, BC
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2003, 284 (04): : G713 - G721
  • [9] Role of NF-κB on liver cold ischemia-reperfusion injury
    Takahashi, Y
    Ganster, RW
    Gambotto, A
    Shao, LF
    Kaizu, T
    Wu, T
    Yagnik, GP
    Nakao, A
    Tsoulfas, G
    Ishikawa, T
    Okuda, T
    Geller, DA
    Murase, N
    AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2002, 283 (05): : G1175 - G1184
  • [10] Melatonin attenuates hepatic ischemia-reperfusion injury in rats by inhibiting NF-κB signaling pathway
    Gao, Yao
    Li, Zhi-Tao
    Jin, Li
    Lin, Jie
    Fan, Zheng-Lei
    Zeng, Zhong
    Huang, Han-Fei
    HEPATOBILIARY & PANCREATIC DISEASES INTERNATIONAL, 2021, 20 (06) : 551 - 560