Prevention of N-nitrosodiethylamine-induced hepatocarcinogenesis by S-allylcysteine

Mol Cell Biochem. 2008 Mar;310(1-2):209-14. doi: 10.1007/s11010-007-9682-4. Epub 2008 Jan 6.

Abstract

Chemopreventive effect of S-allylcysteine (constituent of garlic) on N-nitrosodiethylamine (NDEA)-induced hepatocarcinogenesis was evaluated in Wistar rats. Significantly decreased lipid peroxidation products (thiobarbituric acid reactive substances-TBARS and lipid hydroperoxides) with increased level of reduced glutathione, increased activities of glutathione S-transferase, and glutathione peroxidase were observed in liver of NDEA-treated rats when compared with control rats. The activities of superoxide dismutase and catalase were significantly decreased in tumor tissue when compared with control. Administration of S-allylcysteine (SAC) showed the inhibition of tumor incidence, modulated the lipid peroxidation, and increased the reduced glutathione, glutathione-dependent enzymes, superoxide dismutase, and catalase in NDEA-induced carcinogenesis. From our results, we speculate that S-allylcysteine mediates its chemopreventive effects by modulating lipid peroxidation, GST stimulation, and by increasing the antioxidants. Hence SAC prevents cells from loss of oxidative capacity in NDEA-induced hepatocarcinogenesis.

MeSH terms

  • Animals
  • Catalase / metabolism
  • Cysteine / analogs & derivatives*
  • Cysteine / pharmacology
  • Diethylnitrosamine
  • Glutathione / metabolism
  • Glutathione Peroxidase / metabolism
  • Glutathione Transferase / metabolism
  • Lipid Peroxidation / drug effects
  • Liver / drug effects
  • Liver / enzymology
  • Liver / pathology
  • Liver Neoplasms, Experimental / pathology*
  • Liver Neoplasms, Experimental / prevention & control*
  • Male
  • Precancerous Conditions / pathology*
  • Precancerous Conditions / prevention & control*
  • Rats
  • Rats, Wistar
  • Superoxide Dismutase / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Thiobarbituric Acid Reactive Substances
  • Diethylnitrosamine
  • S-allylcysteine
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Glutathione Transferase
  • Glutathione
  • Cysteine