The Dietary Supplement γ-Oryzanol Attenuates Hepatic Ischemia Reperfusion Injury via Inhibiting Endoplasmic Reticulum Stress and HMGB1/NLRP3 Inflammasome

被引:12
|
作者
Du, Yichao [1 ,2 ]
Zhong, Furui [3 ]
Cheng, Huanli [2 ]
Li, Tongxi [2 ]
Chen, Yifan [2 ]
Tan, Peng [1 ,2 ]
Huang, Meizhou [1 ]
Liang, Tiancheng [4 ]
Liu, Yu [5 ]
Xia, Xianming [1 ,2 ]
Fu, Wenguang [1 ,2 ,6 ]
机构
[1] Southwest Med Univ, Affiliated Hosp, Workstn Sichuan Prov, Luzhou 646000, Peoples R China
[2] Southwest Med Univ, Affiliated Hosp, Dept Hepatobiliary Surg, Luzhou 646000, Peoples R China
[3] Zigong Fourth Peoples Hosp, Dept Gen Surg, Zigong 643000, Peoples R China
[4] Luzhou Municipal Hosp Tradit Chinese Med, Luzhou 646000, Peoples R China
[5] Xichang Peoples Hosp, Xichang 615000, Peoples R China
[6] Nucl Med & Mol Imaging Key Lab Sichuan Prov, Luzhou 646000, Peoples R China
关键词
APPROVED RECOMMENDATION 1985; LIVER-INJURY; 2-OXOGLUTARATE AMINOTRANSFERASE; CATALYTIC CONCENTRATION; IFCC METHODS; MECHANISM; CELL; SUPPRESSION; ACTIVATION; REDUCTION;
D O I
10.1155/2021/4628050
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The purpose of this study is to investigate the protective effect of gamma-oryzanol (ORY) against hepatic ischemia reperfusion (HIR) injury and the potential protective mechanisms of ORY. ORY is an important biologically active ingredient isolated from rice bran oil, which has anti-inflammatory and antiapoptotic effects. However, it is still unknown whether ORY can protect the liver from the HIR damage. In this study, ORY was administered orally for seven days, after which the animals were subjected to liver ischemia for 60 minutes and reperfused for 6 hours. Related indicators were analyzed. The results showed that ORY pretreatment significantly reduced the levels of AST and ALT, relieved hepatocellular damage and apoptosis, and attenuated the exhaustion of SOD and GSH and accumulation of MDA and MPO. Interestingly, ORY treatment could significantly decreased ER stress. Furthermore, ORY pretreatment remarkably reduced the protein expressions of HMGB1, NLRP3, caspase-1 (p20), and IL-1 beta to protect the liver from I/R-induced inflammasome activation and apoptosis. In conclusion, we demonstrated the potential effect of ORY in modulating oxidative stress, endoplasmic reticulum stress, and inflammasome activation during HIR.
引用
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页数:12
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