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Quercetin decreases liver damage in mice with non-alcoholic steatohepatitis.

Abstract
Non-alcoholic steatohepatitis (NASH) is a frequent condition in obese patients that may progress to end-stage liver disease. This study was designed to evaluate the modulation of this condition by use of quercetin (Q), a flavonoid largely found in vegetable foods, with known anti-inflammatory and antioxidant properties, in the experimental model of non-alcoholic steatohepatitis (NASH) using a diet deficient in methionine and choline (MCD). Male C57BL6 mice were divided into four groups (n = 16): (i) Control plus vehicle (control ration plus carboxymethylcellulose 1% used as vehicle, CO + V); (ii) Control ration plus Q 50 mg/kg (CO + Q); (iii) MCD diet plus vehicle (NASH + V); and (iv) MCD diet plus Q (NASH + Q). Diets were administered for 4 weeks. At the end of the experimental period, liver alterations, bioindicators of oxidative stress and DNA damage were assessed. NASH was diagnosed in 100% of the mice that were fed the MCD diet. In addition, a significant increase in DNA damage in liver tissue from NASH + V group was observed in comparison with CO + V. The group NASH + Q showed a significant decrease in hepatic damage enzymes, lipoperoxidation, DNA damage and a lower degree of macrovesicular steatosis, ballooning and inflammatory process. These findings suggest that Q may have protective effects by improving liver integrity in NASH.
AuthorsEder Marcolin, Luiz Felipe Forgiarini, Graziella Rodrigues, Juliana Tieppo, Greice Stefani Borghetti, Valquiria Linck Bassani, Jaqueline Nascimento Picada, Norma Possa Marroni
JournalBasic & clinical pharmacology & toxicology (Basic Clin Pharmacol Toxicol) Vol. 112 Issue 6 Pg. 385-91 (Jun 2013) ISSN: 1742-7843 [Electronic] England
PMID23331460 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Retracted Publication)
Copyright© 2013 Nordic Pharmacological Society. Published by John Wiley & Sons Ltd.
Chemical References
  • Antioxidants
  • Quercetin
  • Methionine
Topics
  • Animals
  • Antioxidants (administration & dosage, therapeutic use)
  • Choline Deficiency
  • Comet Assay
  • DNA Damage (drug effects)
  • Diet
  • Disease Models, Animal
  • Fatty Liver (etiology, metabolism, pathology, prevention & control)
  • Lipid Peroxidation (drug effects)
  • Liver Function Tests
  • Male
  • Methionine (deficiency)
  • Mice
  • Mice, Inbred C57BL
  • Molecular Structure
  • Oxidative Stress (drug effects)
  • Quercetin (administration & dosage, therapeutic use)

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