Synthesis, estrogenic activity, and anti-osteoporosis effects in ovariectomized rats of resveratrol oligomer derivatives

Eur J Med Chem. 2015 Sep 18:102:26-38. doi: 10.1016/j.ejmech.2015.07.042. Epub 2015 Jul 26.

Abstract

Three series of resveratrol oligomer derivatives were synthesized, including the indenone-type, indene-type and octahydropentalene-type derivatives, among which ten derivatives were novel compounds. Compounds 2, 14f, and 4d were confirmed as ERβ agonists by yeast two-hybrid assay, and compound 2 (isopaucifloral F) was further chosen to evaluate its anti-osteoporosis activity in vivo. Compared with the sham-operated and the positive control groups, isopaucifloral F (10 μg/kg) showed a notable anti-osteoporosis effect in the ovariectomized (OVX) female rats based on a micro-CT analysis and the following measurements: bone mineral density, bone volume/tissue volume, trabecular thickness, trabecular separation/spacing, and the serum biochemical parameters. LD50 of isopaucifloral F was found to be greater than 5 mg/kg and its effective dose (ED) was found to be about 10 μg/kg. Therefore, isopaucifloral F may be a promising lead compound for the treatment of postmenopausal osteoporosis.

Keywords: Bone mineral density; Estrogen receptor; Isopaucifloral F; Micro-CT; Osteoporosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Disease Models, Animal
  • Estrogen Receptor beta / agonists*
  • Estrogens / chemical synthesis
  • Estrogens / pharmacology*
  • Female
  • Osteoporosis / drug therapy*
  • Osteoporosis / surgery
  • Ovariectomy*
  • Rats
  • Rats, Sprague-Dawley
  • Resveratrol
  • Stilbenes / chemical synthesis
  • Stilbenes / chemistry*
  • Stilbenes / pharmacology*

Substances

  • Estrogen Receptor beta
  • Estrogens
  • Stilbenes
  • Resveratrol