Hepatoprotective activity of puerarin against carbon tetrachloride-induced injuries in rats: a randomized controlled trial

Food Chem Toxicol. 2013 Sep:59:90-5. doi: 10.1016/j.fct.2013.05.055. Epub 2013 Jun 10.

Abstract

The protective effects of puerarin on liver damage were evaluated by carbon tetrachloride (CCl₄)-induced hepatotoxicity in rats. Male rats were orally treated with puerarin daily, and received CCl₄ intraperitoneally twice a week for 4 weeks. Our results showed that puerarin at doses of 50, 100, and 200 mg/kg b. w. significantly reduced the elevated activities of serum alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase, and lactate dehydrogenase at least 15%, 17%, 14% and 18%, respectively. In addition, puerarin at different doses significantly decreased (p<0.05) the level of hepatic thiobarbituric acid reactive substances compared to the CCl₄-treated group. Furthermore, the treatment of puerarin was also found to significantly increase the activities of superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glutathione-S-transferase, and glutathione content at least 40%, 12%, 25%, 52%, 17% and 44% in the liver of CCl₄-treated rats, respectively. Liver histopathology also showed that puerarin reduced the incidence of liver lesions induced by CCl₄. The results suggest that puerarin exhibits potent hepatoprotective effects on CCl₄-induced liver damages in rats, and that the hepatoprotective effects of puerarin may be due to both the inhibition of lipid peroxidation and to increase of antioxidant enzymes activity.

Keywords: ALP; ALT; AST; Antioxidant; CAT; Carbon tetrachloride; GPx; GR; GSH; GST; Hepatoprotection; Hepatotoxicity; LDH; Puerarin; SOD; TBARS; alanine aminotransferase; alkaline phosphatase; aspartate aminotransferase; catalase; glutathione; glutathione peroxidase; glutathione reductase; glutathione-S-transferase; lactate dehydrogenase; superoxide dismutase; thiobarbituric acid reactive substances.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antioxidants / administration & dosage
  • Antioxidants / therapeutic use*
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Carbon Tetrachloride Poisoning / blood
  • Carbon Tetrachloride Poisoning / metabolism
  • Carbon Tetrachloride Poisoning / pathology
  • Carbon Tetrachloride Poisoning / prevention & control*
  • Dietary Supplements*
  • Glutathione / metabolism
  • Isoflavones / administration & dosage
  • Isoflavones / therapeutic use*
  • Lipid Peroxidation*
  • Liver / drug effects
  • Liver / metabolism*
  • Liver / pathology
  • Male
  • Oxidation-Reduction
  • Oxidative Stress*
  • Oxidoreductases / blood
  • Oxidoreductases / metabolism
  • Random Allocation
  • Rats
  • Rats, Sprague-Dawley
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Antioxidants
  • Biomarkers
  • Isoflavones
  • Thiobarbituric Acid Reactive Substances
  • Oxidoreductases
  • Glutathione
  • puerarin