Protocatechuic Acid-Mediated miR-219a-5p Activation Inhibits the p66shc Oxidant Pathway to Alleviate Alcoholic Liver Injury

被引:29
作者
Fu, Rong [1 ]
Zhou, Junjun [1 ]
Wang, Ruiwen [1 ]
Sun, Ruiumin [1 ]
Feng, Dongcheng [2 ]
Wang, Zhecheng [1 ]
Zhao, Yan [1 ]
Lv, Li [1 ]
Tian, Xiaofeng [2 ]
Yao, Jihong [1 ]
机构
[1] Dalian Med Univ, Dept Pharmacol, Dalian 116044, Peoples R China
[2] Dalian Med Univ, Affiliated Hosp 2, Dept Gen Surg, Dalian 116044, Peoples R China
关键词
OXIDATIVE STRESS; PROMOTES; SUPPRESSION; EXTRACT; DISEASE;
D O I
10.1155/2019/3527809
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Alcohol abuse has become common worldwide and has been recognized as a major cause of chronic alcoholic liver disease (ALD). ALD encompasses a complex process that includes a broad scope of hepatic lesions, ranging from steatosis to cirrhosis. In particular, reactive oxygen species (ROS) are mainly involved. Numerous studies have shown that p66shc plays a significant role in ALD. Protocatechuic acid (PCA), a dihydroxybenzoic acid that is naturally found in green tea, vegetables, and fruits, has efficient free radical scavenging effects. In this study, we aimed to assess the protective effect of PCA on ALD and to evaluate the microRNA- (miRNA-) p66shc-mediated reduction of ROS formation in ALD. Our results demonstrated that PCA treatment significantly decreased p66shc expression and downstream ROS formation in ALD. miR-219a-5p, which was identified by bioinformatics and experimental analysis, was enhanced by PCA and subsequently suppressed p66shc expression. Importantly, p66shc played an essential role in the protection of PCA-stimulated miR-219a-5p overexpression. Overall, these findings show that PCA-stimulated miR-219a-5p expression mitigates ALD by reducing p66shc-mediated ROS formation. This study may contribute to the development of therapeutic interventions for ALD.
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页数:15
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