Hepatoprotective and hypolipidaemic effects of glycoprotein isolated from Gardenia jasminoides ellis in mice

Clin Exp Pharmacol Physiol. 2006 Oct;33(10):925-33. doi: 10.1111/j.1440-1681.2006.04466.x.

Abstract

The present study was performed to investigate the hepatoprotective and hypolipidaemic effects of a 27 kDa glycoprotein isolated from Gardenia jasminoides Ellis (GJE glycoprotein) in glucose/glucose oxidase (G/GO)-treated BNL CL.2 cells, as well as in CCl4, Triton WR-1339 and corn oil-treated mice. In G/GO-treated BNL CL.2 cells, the results showed that GJE glycoprotein has an inhibitory effect on G/GO-induced cytotoxicity and intracellular reactive oxygen species production. In addition, GJE glycoprotein has an anti-oxidant effect against the lipid peroxidation process in the Fe2+/ascorbic acid system. In CCl4 (1.0 mL/kg)-treated mice, pretreatment with GJE glycoprotein (80 mg/kg) blocked lactate dehydrogenase release and the formation of thiobarbituric acid-reactive substances. In addition, in these mice GJE resulted in increased nitric oxide production and the activation of anti-oxidant enzymes, accompanied by the inhibition of the cytotoxic-related signals hepatic cytochrome c, nuclear factor-kappaB and activator protein-1. In both Triton WR-1339 (400 mg/kg) and corn oil (1.0 g/kg)-treated mice, pretreatment with GJE glycoprotein (80 mg/kg) lowered the levels of plasma lipoproteins (triglyceride, total cholesterol and low-density lipoprotein). On the basis of these results, we assume that GJE glycoprotein can ameliorate liver function, because it has hepatoprotective and hypolipidaemic activities.

Publication types

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

MeSH terms

  • Animals
  • Antioxidants / metabolism
  • Carbon Tetrachloride / toxicity
  • Corn Oil / adverse effects
  • Cytochromes c / metabolism
  • Drug Evaluation, Preclinical
  • Gardenia / chemistry*
  • Glycoproteins / isolation & purification*
  • Glycoproteins / pharmacology*
  • Hyperlipidemias / chemically induced
  • Hypolipidemic Agents / isolation & purification
  • Hypolipidemic Agents / pharmacology
  • L-Lactate Dehydrogenase / blood
  • Lipid Peroxidation / drug effects
  • Liver / drug effects*
  • Liver / enzymology
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred ICR
  • NF-kappa B / metabolism
  • Nitric Oxide / blood
  • Polyethylene Glycols / adverse effects
  • Reactive Oxygen Species / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism
  • Transcription Factor AP-1 / metabolism

Substances

  • Antioxidants
  • Glycoproteins
  • Hypolipidemic Agents
  • NF-kappa B
  • Reactive Oxygen Species
  • Thiobarbituric Acid Reactive Substances
  • Transcription Factor AP-1
  • Nitric Oxide
  • Polyethylene Glycols
  • Corn Oil
  • Cytochromes c
  • Carbon Tetrachloride
  • L-Lactate Dehydrogenase
  • tyloxapol