Hepatoprotection of chlorella against carbon tetrachloride-induced oxidative damage in rats

In Vivo. Sep-Oct 2009;23(5):747-54.

Abstract

The effects of 80% ethanolic chlorella extracts (GPE) on carbon tetrachloride (CCl(4))-induced hepatic damage were investigated in Sprague-Dawley rats. The rats were orally treated with GPE (0.5 g/kg body weight) or silymarin (0.2 g/kg body weight) over four consecutive weeks with administration of CCl(4) (20% CCl(4), 0.5 ml/rat twice a week). The GPE had a significant protective effect against liver injuries, as well as oxidative stress induced by CCl(4), resulting in reduced lipid peroxidation and improved serum biochemical parameters such as aspartate aminotransferase and alanine aminotransferase. The reduced levels of glutathione, vitamin C, superoxide dismutase, and catalase in the CCl(4)-treated rats were significantly increased by treatment with GPE. Furthermore, the activity of GPE was comparable to the standard drug silymarin. In conclusion, chlorella may be useful as a hepatoprotective agent against chemical-induced liver damage in vivo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alanine Transaminase / blood
  • Animals
  • Antioxidants / pharmacology*
  • Ascorbic Acid / blood
  • Aspartate Aminotransferases / blood
  • Carbon Tetrachloride
  • Catalase / blood
  • Chemical and Drug Induced Liver Injury / etiology
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Chlorella / chemistry*
  • Glutathione / blood
  • Lipid Peroxidation / drug effects
  • Male
  • Oxidative Stress / drug effects*
  • Plant Extracts / pharmacology*
  • Rats
  • Rats, Sprague-Dawley
  • Silymarin / pharmacology
  • Superoxide Dismutase / blood

Substances

  • Antioxidants
  • Plant Extracts
  • Silymarin
  • Carbon Tetrachloride
  • Catalase
  • Superoxide Dismutase
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Glutathione
  • Ascorbic Acid