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Quantitation of human uptake of the anticarcinogen phenethyl isothiocyanate after a watercress meal.

Abstract
Our previous studies showed that phenethyl isothiocyanate (PEITC), a cruciferous vegetable constituent, inhibited the lung tumorigenesis induced by a potent tobacco-specific carcinogenic nitrosamine in animals. These results implicate dietary PEITC as a risk-reducing factor of lung cancers induced by smoking. To define the effect of dietary PEITC on human cancers, a method of measuring its uptake is needed. Since watercress is rich in gluconasturtiin, a glucosinolate precursor of PEITC, it was chosen to be the source of PEITC. Four individuals were asked to eat watercress as part of a breakfast meal, and 24-h urine samples were collected. A urinary metabolite was found, and its identity was confirmed as the N-acetylcysteine conjugate of PEITC by comparison with the synthetic standard using nuclear magnetic resonance and mass spectrometry. A dose-dependent excretion of this conjugate was observed. These results clearly showed that PEITC was released in the human body upon ingestion of watercress and suggest that the N-acetylcysteine conjugate of PEITC may be a useful marker for quantitating human exposure to this anticarcinogen as a tool for epidemiological investigations.
AuthorsF L Chung, M A Morse, K I Eklind, J Lewis
JournalCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology (Cancer Epidemiol Biomarkers Prev) 1992 Jul-Aug Vol. 1 Issue 5 Pg. 383-8 ISSN: 1055-9965 [Print] United States
PMID1305471 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Anticarcinogenic Agents
  • Glucosinolates
  • Isothiocyanates
  • Thiocyanates
  • phenethyl isothiocyanate
Topics
  • Animals
  • Anticarcinogenic Agents (metabolism, pharmacokinetics, urine)
  • Chromatography, High Pressure Liquid (methods, standards)
  • Dose-Response Relationship, Drug
  • Eating
  • Evaluation Studies as Topic
  • Female
  • Glucosinolates (chemistry, metabolism)
  • Humans
  • Isothiocyanates
  • Lung Neoplasms (diet therapy, prevention & control)
  • Magnetic Resonance Spectroscopy
  • Male
  • Mass Spectrometry
  • Metabolic Clearance Rate
  • Mice
  • Thiocyanates (metabolism, pharmacokinetics, urine)
  • Vegetables

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