Evaluation of the post-initiation effects of oltipraz on aflatoxin B1-induced preneoplastic foci in a rat model of hepatic tumorigenesis.

Previous studies have demonstrated that ingestion of 5-(2-pyrazinyl)-4-methyl-1,2-dithiole-3-thione (oltipraz) during the aflatoxin B1 (AFB1) treatment phase completely prevented hepatic cancer. In this study we evaluated the effect of feeding oltipraz during the post-AFB1 treatment phase. Fifty-five male F344 rats were divided into five groups. All rats were gavaged with 25 micrograms AFB1/rat, five times a week for two successive weeks. The rats were fed the oltipraz-supplemented diet according to three different feeding regimes: during the AFB1 treatment phase (1 week prior to, during and 1 week after the last gavage with AFB1); during the post-treatment phase; or throughout the entire time of the experiment. Phenobarbital-supplemented diet was fed during post-treatment phase to one group and this was used as a positive control for the promotion of AFB1-induced focal growth. The burden of putative, preneoplastic, hepatic glutathione S-transferase P-positive foci was evaluated at 13 weeks after the AFB1 treatment phase. As seen previously, oltipraz fed during the AFB1 treatment phase significantly inhibited focal development, i.e. the volume percent of the liver occupied with foci was reduced by 87%. Oltipraz when fed during the post-treatment phase neither inhibited nor enhanced focal development.
AuthorsY Y Maxuitenko, D L MacMillan, T W Kensler, B D Roebuck
JournalCarcinogenesis (Carcinogenesis) Vol. 14 Issue 11 Pg. 2423-5 (Nov 1993) ISSN: 0143-3334 [Print] ENGLAND
PMID8242875 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Anticarcinogenic Agents
  • Pyrazines
  • oltipraz
  • Aflatoxin B1
  • Glutathione Transferase
  • Aflatoxin B1 (toxicity)
  • Animals
  • Anticarcinogenic Agents (pharmacology)
  • Body Weight (drug effects)
  • Glutathione Transferase (analysis)
  • Liver (drug effects, pathology)
  • Liver Neoplasms, Experimental (chemically induced, pathology, prevention & control)
  • Male
  • Organ Size (drug effects)
  • Precancerous Conditions (chemically induced, pathology, prevention & control)
  • Pyrazines (pharmacology)
  • Rats
  • Rats, Inbred F344
  • Time Factors

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 network!

Choose Username:
Verify Password: