Induction of hepatic estrogen sulfotransferase expression by hypophysectomy in female rats

J Steroid Biochem Mol Biol. 1995 Nov;55(2):255-9. doi: 10.1016/0960-0760(95)00173-w.

Abstract

We have examined the effects of hypophysectomy and treatment with thyroxine (T4) on enzyme activity and expression (as determined by immunoblot analysis) of members of the three principal sulfotransferase (ST) sub-families (phenol STs, PST; estrogen STs, EST; hydroxysteroid STs, HST) in cytosols prepared from female Wistar rat livers. The results demonstrate that in female rat liver cytosol, EST activity was decreased by treatment with T4, increased following hypophysectomy and that treatment of hypophysectomized animals with T4 also greatly reduced EST activity. T4 had no significant effect on PST or HST activity in normal animals, but it decreased HST activity in hypophysectomized rat liver cytosol. Immunoblot analysis of these cytosols with antibodies recognising HST and PST indicated that where changes in enzyme activity occurred they mirrored changes in enzyme protein expression. In normal adult female rat livers, EST protein is not expressed, and the small residual activity results predominantly from the action of HST. Hypophysectomy induced EST activity and the expression of EST enzyme protein in female rat liver cytosol, and T4 treatment of hypophysectomized animals reduced the activity to below normal levels without reducing the corresponding enzyme protein levels, indicating that T4 regulation of EST in females is via a post-translational mechanism.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cytosol / enzymology
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Induction
  • Female
  • Gene Expression* / drug effects
  • Hypophysectomy*
  • Immunoblotting
  • Liver / enzymology*
  • Rats
  • Rats, Wistar
  • Reference Values
  • Substrate Specificity
  • Sulfotransferases / analysis
  • Sulfotransferases / biosynthesis*
  • Sulfotransferases / metabolism
  • Thyroxine / pharmacology*

Substances

  • Sulfotransferases
  • estrone sulfotransferase
  • Thyroxine