Dietary trans-resveratrol bioavailability and effect on CCl4-induced liver lipid peroxidation

J Gastroenterol Hepatol. 2009 Apr;24(4):618-22. doi: 10.1111/j.1440-1746.2008.05598.x. Epub 2008 Sep 24.

Abstract

Background and aim: Several in vitro studies have demonstrated the ability of pure trans-resveratrol (t-Res) to act as an anti-oxidant, but the scientific literature is lacking in in vivo studies dealing with dietary t-Res bioavailability in oxidative stress models. Our aim was to investigate the bioavailability of t-Res from dietary sources and its effect on an animal model of carbon tetrachloride (CCl4)-induced liver lipid peroxidation.

Methods: Ten rats were intragastrically administered for 14 days with a grape-stalk extract determining a daily t-Res dosage of 3 mg/kg. The control group (10 rats) was daily injected with the vehicle solvent without the t-Res extract. After 1 week, the induction of liver lipid peroxidation by CCl4 injection was carried out. Serum and liver samples, at different time intervals, were collected to evaluate t-Res content, by high-performance liquid chromatography (HPLC) and liquid chromatography-mass spectometry-mass spectometry (LC-MS-MS). Liver malondialdehyde (MDA) as marker of oxidative stress was measured.

Results: t-Res accumulates in the liver reaching 49.8 +/- 10.2 ng/g after 7 days and 191.8 +/- 15.3 ng/g after 14 days. No t-Res was detected in serum. The increase of MDA liver concentration due to CCl4 injection after 24 h and 1 week was reduced by 38% and a 63%, respectively, by the treatment with the t-Res extract.

Conclusions: A moderate consumption of t-Res from a dietary source resulted in a time-dose-dependent liver accumulation. It was able to counteract in vivo CCl4-induced liver lipid peroxidation thus demonstrating the hepatoprotective property of t-Res.

MeSH terms

  • Animals
  • Antioxidants / administration & dosage*
  • Antioxidants / isolation & purification
  • Antioxidants / pharmacokinetics
  • Biological Availability
  • Carbon Tetrachloride
  • Chemical and Drug Induced Liver Injury
  • Cytoprotection
  • Diet
  • Disease Models, Animal
  • Intubation, Gastrointestinal
  • Lipid Peroxidation / drug effects*
  • Liver / drug effects*
  • Liver / metabolism
  • Liver Diseases / metabolism
  • Liver Diseases / prevention & control*
  • Male
  • Malondialdehyde / metabolism
  • Plant Stems
  • Rats
  • Rats, Sprague-Dawley
  • Resveratrol
  • Stilbenes / administration & dosage*
  • Stilbenes / blood
  • Stilbenes / isolation & purification
  • Stilbenes / pharmacokinetics
  • Vitis* / chemistry

Substances

  • Antioxidants
  • Stilbenes
  • Malondialdehyde
  • Carbon Tetrachloride
  • Resveratrol