Literature DB >> 26921731

Protective effect of wedelolactone against CCl4-induced acute liver injury in mice.

Yang Lu1, DongMei Hu2, ShanBo Ma3, Xian Zhao2, Shan Wang2, Guo Wei2, XiFang Wang3, AiDong Wen2, JingWen Wang4.   

Abstract

Eclipta, a traditional Chinese medicine, has been used to treat liver disease for centuries. However, the chemical basis and biological mechanisms of Eclipta remain elusive. The current study aims to investigate the hepatoprotective effect of wedelolactone (WEL), a major coumarin in Eclipta, using C57BL/6 mice with carbon tetrachloride CCl4-induced acute liver injury (ALI). Our data showed that WEL markedly decreased the CCl4-induced elevation of serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) activities, and improved hepatic histopathology changes. WEL also significantly decreased the content of MDA in liver tissues, meanwhile increased the activities of antioxidant enzymes SOD and GSH-Px. In addition, WEL reduced the protein expression of TNF-α, IL-1β and IL-6, as well as mRNA expression. Western blot results revealed that WEL repressed phosphorylation of extracellular signal-regulated kinase (ERK) and translocation of NF-κB p65 from cytoplasm to nucleus and enhanced the phosphorylation of c-Jun. N-terminal kinase (JNK). Moreover, results showed that WEL significantly inhibited CCl4-induced hepatocytes apoptosis, markedly suppressed the down-regulation of Bax and active Caspase-3 expression and accelerated the expression of Bcl-2. Overall, the findings indicate that WEL exhibits a protective effect against CCl4-induced ALI in mice by enhancing the antioxidative defense system, suppressing the inflammatory response and cell apoptosis of liver.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Acute liver injury; Apoptosis; Hepatoprotective action; Inflammatory response; Oxidative stress; Wedelolactone

Mesh:

Substances:

Year:  2016        PMID: 26921731     DOI: 10.1016/j.intimp.2016.02.003

Source DB:  PubMed          Journal:  Int Immunopharmacol        ISSN: 1567-5769            Impact factor:   4.932


  19 in total

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