Biological and Pharmaceutical Bulletin · 2010 · 225 citations · 18 references
Veterinary MedicineBiochemistryNutritional SciencesHepatotoxicologyInflammationMetabolismChemical-induced HepatotoxicityHepatic ImpairmentHepatotoxicity MechanismsOxidative Stress In HepatotoxicityFree Radical ScavengingHepatoprotective AgentsLignin-degrading EnzymesLiver Injury ModelsOxidative Stress InjuryPhenolic Defense CompoundsSerum Alanine AminotransferaseSerum Aspartate Aminotransferase
The mycelia of the edible mushroom Lentinula edodes can be cultured in solid medium containing lignin, and the hot-water extracts (L.E.M.) is commercially available as a nutritional supplement. During the cultivation, phenolic compounds, such as syringic acid and vanillic acid, were produced by lignin-degrading peroxidase secreted from L. edodes mycelia. Since these compounds have radical scavenging activity, we examined their protective effect on oxidative stress in mice with CCl(4)-induced liver injury. We examined the hepatoprotective effect of syringic acid and vanillic acid on CCl(4)-induced chronic liver injury in mice. The injection of CCl(4) into the peritoneal cavity caused an increase in the serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. The intravenous administration of syringic acid and vanillic acid significantly decreased the levels of the transaminases. Four weeks of CCl(4) treatment caused a sufficiently excessive deposition of collagen fibrils. An examination of Azan-stained liver sections revealed that syringic acid and vanillic acid obviously suppressed collagen accumulation and significantly decreased the hepatic hydroxyproline content, which is the quantitative marker of fibrosis. Both of these compounds inhibited the activation of cultured hepatic stellate cells, which play a central role in liver fibrogenesis, and maintained hepatocyte viability. These data suggest that the administration of syringic acid and vanillic acid could suppress hepatic fibrosis in chronic liver injury.
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Anticancer potential of curcumin: preclinical and clinical studies.
Bharat B. Aggarwal, Anushree Kumar, Alok C. Bharti · PubMed · 2003 · 2.6K citations
Medicine, Oncology, Pharmacology +15
Sita Aggarwal, Haruyo Ichikawa, Yasunari Takada et al. · Molecular Pharmacology · 2005 · 530 citations
Medicine, Oncology, Pharmacology +13