Literature DB >> 19833181

Hepatoprotective effects of an active part from Artemisia sacrorum Ledeb. against acetaminophen-induced toxicity in mice.

Hai-Dan Yuan1, Guang-Zhu Jin, Guang-Chun Piao.   

Abstract

AIMS OF STUDY: Although Artemisia sacrorum Ledeb. (Compositae) has long been used as one kind of oriental folk medicine to treat some liver diseases, the underlying mechanism(s) by which these effects are induced remains to be defined. This study was designed to investigate the hepatoprotective effects of 50% ethanol eluate precipitation of Artemisia sacrorum Ledeb. (EEP) on acetaminophen (APAP)-induced toxicity in mice.
MATERIALS AND METHODS: The levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and tumor necrosis factor-alpha (TNF-alpha) levels in mouse sera, and glutathione (GSH), malondialdehyde (MDA) in mouse liver tissues were measured. In addition, apoptosis and necrosis were evaluated by liver histopathological analysis and DNA laddering. Moreover, caspase-3 and -8 protein expressions in mouse livers were observed by Western blot analysis.
RESULTS: Pretreated with EEP prior to the administration of APAP significantly prevented the increases of AST, ALT, and TNF-alpha levels in sera, and suppressed the GSH depletion, MDA accumulation in liver tissues markedly. In addition, EEP prevented APAP-induced apoptosis and necrosis, as indicated by liver histopathological analysis, immunohistochemical analysis, and DNA laddering. Furthermore, according to the results from Western blot analysis, EEP decreased APAP-induced caspase-3 and caspase-8 protein expressions in mouse livers markedly.
CONCLUSION: All these results suggest that the protective effects of EEP against APAP-induced liver injury may involve mechanisms associated with its inhibitive effects of lipid peroxidation and the down-regulation of TNF-alpha mediated apoptosis. In a word, EEP could be a valuable candidate for further development for prevention and treatment of hepatic injury. Copyright 2009 Elsevier Ireland Ltd. All rights reserved.

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Year:  2009        PMID: 19833181     DOI: 10.1016/j.jep.2009.10.002

Source DB:  PubMed          Journal:  J Ethnopharmacol        ISSN: 0378-8741            Impact factor:   4.360


  15 in total

1.  Flavonoids from Artemisia sacrorum Ledeb. and their cytotoxic activities against human cancer cell lines.

Authors:  Haidan Yuan; Xuyang Lu; Qianqian Ma; Di Li; Guanghua Xu; Guangchun Piao
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Review 4.  Models of drug-induced liver injury for evaluation of phytotherapeutics and other natural products.

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Journal:  Food Chem Toxicol       Date:  2013-01-22       Impact factor: 6.023

5.  Toxicological evaluation of Terminalia paniculata bark extract and its protective effect against CCl4-induced liver injury in rodents.

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6.  Bazhen decoction protects against acetaminophen induced acute liver injury by inhibiting oxidative stress, inflammation and apoptosis in mice.

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Review 7.  Oxidative stress during acetaminophen hepatotoxicity: Sources, pathophysiological role and therapeutic potential.

Authors:  Kuo Du; Anup Ramachandran; Hartmut Jaeschke
Journal:  Redox Biol       Date:  2016-10-04       Impact factor: 11.799

8.  Mechanistic Modelling of Drug-Induced Liver Injury: Investigating the Role of Innate Immune Responses.

Authors:  Lisl Km Shoda; Christina Battista; Scott Q Siler; David S Pisetsky; Paul B Watkins; Brett A Howell
Journal:  Gene Regul Syst Bio       Date:  2017-05-30

9.  Protective Effect of Silymarin against Acrolein-Induced Cardiotoxicity in Mice.

Authors:  Elahe Taghiabadi; Mohsen Imenshahidi; Khalil Abnous; Fatemeh Mosafa; Mojtaba Sankian; Bahram Memar; Gholamreza Karimi
Journal:  Evid Based Complement Alternat Med       Date:  2012-12-18       Impact factor: 2.629

10.  Hepatoprotective activity of Mammea africana ethanol stem bark extract.

Authors:  Jude Efiom Okokon; Michael Burata Bawo; Herbert Orji Mbagwu
Journal:  Avicenna J Phytomed       Date:  2016 Mar-Apr
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