1. Academic Validation
  2. Dihydroquercetin ameliorated acetaminophen-induced hepatic cytotoxicity via activating JAK2/STAT3 pathway and autophagy

Dihydroquercetin ameliorated acetaminophen-induced hepatic cytotoxicity via activating JAK2/STAT3 pathway and autophagy

  • Appl Microbiol Biotechnol. 2018 Feb;102(3):1443-1453. doi: 10.1007/s00253-017-8686-6.
Wenjing Zai  # 1 Wei Chen  # 2 Jingyun Luan 2 Jiajun Fan 2 Xuyao Zhang 2 Zimei Wu 1 Tao Ding 2 Dianwen Ju 2 Hongrui Liu 3
Affiliations

Affiliations

  • 1 Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, People's Republic of China.
  • 2 Department of Microbiological and Biochemical Pharmacy & The Key Laboratory of Smart Drug Delivery, Ministry of Education, School of Pharmacy, Fudan University, Shanghai, 201203, People's Republic of China.
  • 3 Department of Pharmacology, School of Pharmacy, Fudan University, Shanghai, 201203, People's Republic of China. [email protected].
  • # Contributed equally.
Abstract

Acetaminophen (APAP) overdose is currently the leading cause of acute liver disease, but therapeutic treatment strategies are commonly limited. Although dihydroquercetin (DHQ) is an attractive botanical antioxidant, its protective potential for liver disease remains elusive. The present study investigated the protective effects of DHQ against APAP-induced hepatic cytotoxicity. Primary mouse hepatocytes were treated with different concentrations of DHQ followed by APAP administration. Our data showed that DHQ relieved APAP-induced growth inhibition and Lactate Dehydrogenase (LDH) release in a dose-dependent manner, as well as inhibited APAP-induced necrosis and extracellular signal regulated kinase-c-Jun-N-terminal kinase (ERK-JNK) stress. In addition, Reactive Oxygen Species (ROS) accumulation and mitochondria dysfunction were also reversed by DHQ treatment. Further study revealed that DHQ induced phosphorylation of Janus kinase 2/signal transducer and activator of transcription 3 (JAK2/STAT3) cascade and thus modulated expression of anti-apoptotic Bcl-2 Family proteins. Moreover, DHQ induced Autophagy which mediated its protective effects in hepatocytes. The protection was abrogated through pharmacological blockage of Autophagy by chloroquine (CQ). These studies demonstrated, for the first time, that DHQ possessed hepatocellular protective effects in the context of APAP-induced cytotoxicity and subsequently revealed that the mechanisms comprised activation of JAK2/STAT3 signaling pathway and Autophagy. These altogether highlighted the significant therapeutic potential of this agent during acute liver failure and other types of liver diseases.

Keywords

Acetaminophen; Autophagy; Dihydroquercetin; Hepatic cytotoxicity; JAK2/STAT3.

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