Antioxidant enzymatically modified isoquercitrin suppresses the development of liver preneoplastic lesions in rats induced by beta-naphthoflavone

Toxicology. 2010 Feb 9;268(3):213-8. doi: 10.1016/j.tox.2009.12.019. Epub 2010 Jan 5.

Abstract

To investigate the modifying effect of enzymatically modified isoquercitrin (EMIQ) on hepatocellular tumor promotion induced by beta-naphthoflavone (BNF) treatment, male rats were administered a single intraperitoneal injection of N-diethylnitrosamine (DEN) and were fed a diet containing BNF (0.5%) for 6 weeks with or without EMIQ (0.2%) in the drinking water after DEN initiation. One week after the commencement of the administration of BNF, rats were subjected to a two-thirds partial hepatectomy. The number and area of GST-P positive foci, the number of COX2-positive cells and the area of elastica-van Gieson (EVG)-positive connective tissue fibers promoted by BNF were significantly suppressed by the administration of the antioxidant EMIQ. Real-time RT-PCR analysis revealed that EMIQ treatment decreased mRNA expression levels of Gstm1, Serpine1, Cox2 and Nfkbia and increased mRNA expression levels of Yc2 compared with those in the DEN-BNF group. These results suggest that co-administration of EMIQ suppresses the hepatocellular tumor-promoting activity of BNF in rats through the anti-inflammatory effects of EMIQ and restores the cellular redox balance altered by BNF.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anticarcinogenic Agents*
  • Antioxidants / chemistry*
  • Antioxidants / pharmacology*
  • Connective Tissue / drug effects
  • Connective Tissue / metabolism
  • Cyclooxygenase 2 / metabolism
  • Glutathione Peroxidase / metabolism
  • Immunohistochemistry
  • Liver Neoplasms, Experimental / chemically induced
  • Liver Neoplasms, Experimental / pathology
  • Male
  • Precancerous Conditions / pathology
  • Precancerous Conditions / prevention & control*
  • Quercetin / analogs & derivatives*
  • Quercetin / chemistry
  • Quercetin / pharmacology
  • RNA, Messenger / biosynthesis
  • RNA, Messenger / genetics
  • Rats
  • Rats, Inbred F344
  • Reverse Transcriptase Polymerase Chain Reaction
  • beta-Naphthoflavone / antagonists & inhibitors*
  • beta-Naphthoflavone / toxicity*

Substances

  • Anticarcinogenic Agents
  • Antioxidants
  • RNA, Messenger
  • isoquercitrin
  • beta-Naphthoflavone
  • Quercetin
  • Glutathione Peroxidase
  • Cyclooxygenase 2