Absorption and metabolism of genistin in the isolated rat small intestine

FEBS Lett. 2000 Jun 16;475(2):127-30. doi: 10.1016/s0014-5793(00)01642-2.

Abstract

Uptake and intestinal metabolism of physiologically active genistin were studied in an ex vivo intestinal perfusion model; luminally applied concentrations were 5.9, 12.0, and 23.8 micromol/l. The intestinal absorption of genistin was 14.9% (+/-2.3, n=9), irrespective of the amounts applied. The majority of the absorbed genistin appeared as genistein glucuronide (11.6%), also recovered as the main metabolite on the luminal side (19.5%). Minor amounts of genistin (1.3%) and genistein (1.9%) were found on the vascular side, whereas 15.4% of applied genistin was luminally cleaved to yield genistein. Sulfate derivatives of genistein or genistin were not observed.

MeSH terms

  • Animals
  • Chromatography, High Pressure Liquid
  • Dose-Response Relationship, Drug
  • Estrogens, Non-Steroidal / pharmacokinetics*
  • Genistein / metabolism
  • Glucuronic Acid / metabolism
  • Intestinal Absorption*
  • Intestine, Small / drug effects*
  • Intestine, Small / metabolism*
  • Isoflavones / pharmacokinetics*
  • Male
  • Perfusion
  • Rats
  • Rats, Sprague-Dawley
  • Time Factors

Substances

  • Estrogens, Non-Steroidal
  • Isoflavones
  • genistin
  • Glucuronic Acid
  • Genistein