HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

A glucosinolate-rich extract of Japanese Daikon perturbs carcinogen-metabolizing enzyme systems in rat, being a potent inducer of hepatic glutathione S-transferase.

AbstractPURPOSE:
Glucosinolates/isothiocyanates are an established class of naturally occurring chemopreventive agents, a principal mechanism of action being to limit the generation of genotoxic metabolites of chemical carcinogens, as a result of modulation of cytochrome P450 and phase II detoxification enzymes. The objective of this study was to assess whether a glucosinolate-rich extract from Daikon sprouts, containing glucroraphasatin and glucoraphenin, is a potential chemopreventive agent by modulating such enzymes in the liver and lung of rats.
METHODS:
Rats were exposed to the glucosinolate-rich Daikon extract through the diet, at three dose levels, for 14 days, so that the low dose simulates dietary intake.
RESULTS:
At the low dose only, a modest increase was noted in the hepatic dealkylations of methoxy-, ethoxy-, pentoxyresorufin and benzyloxyquinoline that was accompanied by elevated expression of CYP1 and CYP3A2 apoprotein levels. In lung, only a modest increase in the dealkylation of pentoxyresorufin was observed. At higher doses, in both tissues, these increases were abolished. At the same low dietary dose, the Daikon extract elevated markedly glutathione S-transferase activity paralleled by rises in GSTα, GSTμ and GSTπ protein expression. An increase was also noted in quinone reductase activity and expression. Finally, glucuronosyl transferase and epoxide hydrolase activities and expression were also up-regulated, but necessitated higher doses.
CONCLUSION:
Considering the ability of Daikon glucosinolates to effectively enhance detoxification enzymes, in particular glutathione S-transferase, it may be inferred that consumption of this vegetable may possess significant chemopreventive activity and warrants further evaluation through epidemiology and studies in animal models of cancer.
AuthorsAhmad Faizal Abdull Razis, Gina Rosalinda De Nicola, Eleonora Pagnotta, Renato Iori, Costas Ioannides
JournalEuropean journal of nutrition (Eur J Nutr) Vol. 52 Issue 3 Pg. 1279-85 (Apr 2013) ISSN: 1436-6215 [Electronic] Germany
PMID22710810 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Anticarcinogenic Agents
  • Carcinogens
  • Glucosinolates
  • Isoenzymes
  • Plant Extracts
  • Cytochrome P-450 Enzyme System
  • Quinone Reductases
  • Glucuronosyltransferase
  • Glutathione Transferase
  • Epoxide Hydrolases
Topics
  • Animals
  • Anticarcinogenic Agents (administration & dosage, metabolism)
  • Carcinogens (metabolism)
  • Cytochrome P-450 Enzyme System (biosynthesis, metabolism)
  • Dietary Supplements
  • Enzyme Induction
  • Epoxide Hydrolases (biosynthesis, metabolism)
  • Glucosinolates (administration & dosage, metabolism)
  • Glucuronosyltransferase (biosynthesis, metabolism)
  • Glutathione Transferase (biosynthesis, metabolism)
  • Isoenzymes (biosynthesis, metabolism)
  • Liver (enzymology, metabolism)
  • Male
  • Plant Extracts (administration & dosage, metabolism)
  • Plant Shoots (chemistry)
  • Quinone Reductases (biosynthesis, metabolism)
  • Random Allocation
  • Raphanus (chemistry)
  • Rats
  • Rats, Wistar

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: