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

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

  • Oxid Med Cell Longev. 2019 Jul 24;2019:3527809. doi: 10.1155/2019/3527809.
Rong Fu 1 Junjun Zhou 1 Ruiwen Wang 1 Ruimin Sun 1 Dongcheng Feng 2 Zhecheng Wang 1 Yan Zhao 1 Li Lv 1 Xiaofeng Tian 2 Jihong Yao 1
Affiliations

Affiliations

  • 1 Department of Pharmacology, Dalian Medical University, Dalian 116044, China.
  • 2 Department of General Surgery, The Second Affiliated Hospital of Dalian Medical University, Dalian 116044, China.
Abstract

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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