Hepatoprotective effects of Lycium chinense Miller fruit and its constituent betaine in CCl4-induced hepatic damage in rats

Acta Histochem. 2014 Jul;116(6):1104-12. doi: 10.1016/j.acthis.2014.05.004. Epub 2014 Jul 2.

Abstract

The hepatoprotective activities of Lycium chinense Miller (LC) fruit extract and its component betaine were investigated under carbon tetrachloride (CCl4)-induced hepatotoxicity in rats. The treatment of LC fruit extract significantly suppressed the increase of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in the sera of CCl4 injured rats, and restored the decreased levels of anti-oxidant enzymes such as total antioxidant capacity (TAC), superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPx) and suppressed the expression of inflammatory mediators including inducible nitric oxide synthase (iNOS) and cyclooxygenase (COX)-1 and -2. To visualize the potential activity of betaine, a component of LC fruit, betaine was substituted for LC extract in CCl4 injured rats. The biochemical profile in CCl4 injured rats co-treated with betaine matched those of LC fruit treated CCl4 injured rats. The ameliorative effects of LC extract, as well as betaine, were also confirmed by histopathological examination. Collectively, the present findings imply that LC fruit, via its component betaine, mitigate CCl4-induced hepatic injury by increasing antioxidative activity and decreasing inflammatory mediators including iNOS and COX-1/COX-2.

Keywords: Betaine; Carbon tetrachloride; Hepatotoxicity; Lycium chinense Miller; Rat.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antioxidants / pharmacology*
  • Aspartate Aminotransferases / blood
  • Betaine / pharmacology*
  • Carbon Tetrachloride
  • Chemical and Drug Induced Liver Injury / enzymology
  • Chemical and Drug Induced Liver Injury / immunology
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Cyclooxygenase 1 / metabolism
  • Cyclooxygenase 2 / metabolism
  • Female
  • Fruit / chemistry*
  • Lipid Peroxidation
  • Liver / drug effects
  • Liver / enzymology
  • Liver / pathology
  • Lycium / chemistry*
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Membrane Proteins / metabolism
  • Nitric Oxide Synthase Type II / metabolism
  • Plant Extracts / pharmacology*
  • Rats, Sprague-Dawley

Substances

  • Antioxidants
  • Membrane Proteins
  • Plant Extracts
  • Betaine
  • Carbon Tetrachloride
  • Nitric Oxide Synthase Type II
  • Nos2 protein, rat
  • Cyclooxygenase 1
  • Cyclooxygenase 2
  • Ptgs1 protein, rat
  • Ptgs2 protein, rat
  • Aspartate Aminotransferases
  • Alanine Transaminase