Effect of 2,3,7,8-tetrachlorodibenzo-p-dioxin on the hepatic distribution of iron, copper, zinc, and magnesium in rats

J Biochem Toxicol. 1988 Summer:3:121-9. doi: 10.1002/jbt.2570030206.

Abstract

The distribution of iron, copper, zinc, and magnesium in hepatic subcellular fractions of male and female rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) was determined. Animals received 40 micrograms TCDD per kilogram per day for three days by mouth (po) or the vehicle and were killed seven or nine days posttreatment. Iron, copper, zinc, and magnesium were determined by atomic absorption spectroscopy. The iron content of liver from female animals was twofold higher than male animals. The administration of TCDD increased the iron content of mitochondria in female and male rats and decreased iron content of microsomes of both sexes. Significant increases occurred in the copper content of whole liver, mitochondria, and cytosol of male rats and in whole liver and cytosol of female rats. Decreases in the copper content of the microsomes of male rats were observed following TCDD treatment; however, TCDD produced no changes in the zinc content of hepatic subcellular fractions of either sex. The magnesium content of female TCDD-treated rats increased in whole liver, mitochondria, and cytosol, while the magnesium content of microsomes was not altered. With respect to the subcellular distribution of iron, copper, zinc, and magnesium, TCDD produces differential effects. The altered distribution of some cations may contribute to the broad range of effects of TCDD.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Copper / metabolism*
  • Cytosol / drug effects
  • Cytosol / metabolism
  • Dioxins / pharmacology*
  • Female
  • Iron / metabolism*
  • Liver / drug effects
  • Liver / metabolism*
  • Magnesium / metabolism*
  • Male
  • Microsomes, Liver / drug effects
  • Microsomes, Liver / metabolism
  • Mitochondria, Liver / drug effects
  • Mitochondria, Liver / metabolism
  • Polychlorinated Dibenzodioxins / pharmacology*
  • Rats
  • Rats, Inbred Strains
  • Reference Values
  • Sex Factors
  • Zinc / metabolism*

Substances

  • Dioxins
  • Polychlorinated Dibenzodioxins
  • Copper
  • Iron
  • Magnesium
  • Zinc