Metabolism and disposition of 1,4,7,8-tetrachlorodibenzo-p-dioxin in rats

Chemosphere. 1998 Oct-Nov;37(9-12):1885-93. doi: 10.1016/s0045-6535(98)00255-0.

Abstract

Metabolism studies of 1,4,7,8-tetrachlorodibenzo-p-dioxin (TCDD), a relatively nontoxic dioxin congener, were undertaken to gain a better understanding of mammalian metabolism of dioxins without the problems associated with the use of the most toxic congener, 2,3,7,8-TCDD. 14C-1,4,7,8-TCDD was dosed to conventional and bile-cannulated rats at a level of 8 mg/kg. The 14C was excreted almost entirely in 72 hours with the major routes of excretion feces and bile. Metabolites were identified from the feces, bile, and urine by GC-MS or negative ion FAB MS and 1H NMR. The two major fecal metabolites were hydroxylated tetra- and triCDDs. Glucuronide and sulfate conjugates of these hydroxyl metabolites were found in the urine and bile. Minor metabolites included dichlorocatechol, dihydroxylated tetra- and triCDDs, and conjugates of these compounds.

MeSH terms

  • Animals
  • Body Burden
  • Environmental Pollutants / blood
  • Environmental Pollutants / pharmacokinetics*
  • Environmental Pollutants / urine
  • Feces / chemistry
  • Half-Life
  • Male
  • Polychlorinated Dibenzodioxins / blood
  • Polychlorinated Dibenzodioxins / pharmacokinetics*
  • Polychlorinated Dibenzodioxins / urine
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Environmental Pollutants
  • Polychlorinated Dibenzodioxins