Chlorogenic acid alleviates oxidative damage in hepatocytes by regulating miR-199a-5p/GRP78 axis

被引:8
|
作者
Li, Jiaxin [1 ,2 ]
Ge, Hengju [2 ]
Xu, Yang [2 ,3 ]
Xie, Jiahong [2 ]
Karim, Naymul [1 ,2 ]
Yan, Fujie [2 ]
Mo, Jianling [1 ]
Chen, Wei [1 ,2 ,3 ]
机构
[1] Zhejiang Univ, Sir Run Run Shaw Hosp, Sch Med, Dept Tradit Chinese Med, Hangzhou 310016, Peoples R China
[2] Zhejiang Univ, Coll Biosyst Engn & Food Sci, Dept Food Sci & Nutr, Hangzhou 310058, Peoples R China
[3] Zhejiang Univ, Ningbo Innovat Ctr, Ningbo 315100, Peoples R China
基金
中国国家自然科学基金;
关键词
Chlorogenic acid; Oxidative stress; MiR-199a-5p; GRP78; Hepato-protection; ENDOPLASMIC-RETICULUM STRESS; SIGNAL-TRANSDUCTION; IN-VITRO; PROTEIN; INHIBITION;
D O I
10.1016/j.fbio.2023.102595
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Chlorogenic acid (CGA) is a phenylpropanoid compound in chrysanthemum, which has a variety of biological activities. Nevertheless, CGA has not yet been studied concerning oxidative stress in hepatocytes. Our research aims to investigate whether chlorogenic acid can improve hepatic oxidative stress, and further illustrated its detailed mechanism. The results of free radicals measurement and Western blot showed that CGA suppressed the activation of JNK (c-Jun NH2-teminal kinase) signaling pathway by ameliorating endoplasmic reticulum stress in H2O2-treated hepatocytes, thereby eliminating excess intracellular free radicals. In addition, through RT-qPCR, we found that miR-199a-5p down-regulated in H2O2-induced L02 cells, which was restored by CGA. By inhibiting the expression of miR-199a-5p to promote the transcription of GRP78 gene, the antioxidant capacity of CGA was greatly weakened in hepatocytes. Our findings suggest that CGA treatment alleviated the H2O2-induced oxidative stress by targeting miR-199a-5p, thereby ameliorating ER stress and inhibiting JNK phosphorylation for anti-oxidant capacity enhancement. Based on our available results, CGA may be an alternative compound to mitigate hepatic oxidative damage through the miR-199a-5p/GPR78 axis.
引用
收藏
页数:10
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