Advertisement

Archives of Toxicology

, Volume 75, Issue 2, pp 74–79 | Cite as

Estrogenic potency of benzophenone and its metabolites in juvenile female rats

  • Yoshio Nakagawa
  • Kuniaki Tayama
Molecular Toxicology

Abstract.

The estrogenic activity of benzophenone and its metabolites, benzhydrol and p-hydroxybenzophenone, were investigated in vitro by estrogen receptor (ER) competitive ligand binding assay and in vivo by uterotrophic assay in juvenile female Sprague-Dawley (SD) rats. p-Hydroxybenzophenone as well as diethylstilbestrol and bisphenol A, known xeno-estrogenic compounds, competed with fluorescein-labeled 17β-estradiol to bind human recombinant ERα in a concentration-dependent manner. Fifty percent inhibitory values (IC50) of diethylstilbestrol, bisphenol A, and p-hydroxybenzophenone were approximately 10–8, 10–5, and 5×10–5 M, respectively. However, neither the parent compound nor benzhydrol at concentrations from 10–9 to 5×10–4 M impaired the binding of 17β-estradiol to ERα. Juvenile female rats (21-days-old) were given s.c. injections of benzophenone, its metabolites, and 17β-estradiol for 3 days. Administration of p-hydroxybenzophenone (100–400 mg/kg) elicited an increase in absolute and relative uterine weights in a dose-dependent manner and 17β-estradiol (10 µg/kg) increased uterine weight approximately fourfold relative to control. The uterine response caused by both compounds was accompanied by an increase in luminal epithelial height and stromal cells in the uterus and an increase in thickness of vaginal epithelial cell layers with cornification. In contrast, benzophenone and benzhydrol at a dose of 400 mg/kg affected neither uterine weight nor histological changes of the uterus and vagina. These results indicate that p-hydroxybenzophenone, a metabolite of benzophenone, exhibits intrinsic xeno-estrogenic activity in the female reproductive tract.

Benzophenone Metabolites Uterotrophic assay Competitive binding assay Female rats 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Copyright information

© Springer-Verlag 2001

Authors and Affiliations

  • Yoshio Nakagawa
    • 1
  • Kuniaki Tayama
    • 1
  1. 1.Department of Toxicology, Tokyo Metropolitan Research Laboratory of Public Health, 3-24-1, Hyakunin-cho, Shinjuku-ku, Tokyo 169-0073, Japan

Personalised recommendations