Kanamycin inhibits daidzein metabolism and abilities of the metabolites to prevent bone loss in ovariectomized mice

BMC Res Notes. 2016 Jul 7:9:334. doi: 10.1186/s13104-016-2139-7.

Abstract

Background: Daidzein is an isoflavone derived from soybeans that exerts preventive effects on bone loss in ovariectomized (OVX) animals. These effects have been correlated with increasing serum equol levels. In the present study, we investigated the effects of antibiotic intake on equol metabolism from daidzein, and the corresponding levels of bone loss in OVX mice.

Methods: Eight-week-old female ddY mice (n = 42) were either ovariectomized (OVX) or subjected to a sham operation (sham). OVX mice were then divided into six dietary subgroups: control diet (control), 0.3 % kanamycin diet (KN), 0.1 % daidzein diet (Dz), 0.1 % daidzein and 0.0375 % kanamycin diet (Dz+KN3.75), 0.1 % daidzein and 0.075 % kanamycin diet (Dz+KN7.5), and 0.1 % daidzein and 0.3 % kanamycin diet (Dz+KN30). The mice were fed their respective diets for 4 weeks.

Results: Uterine weight and femoral bone mineral density (BMD) were significantly lower in the OVX mice compared in the sham mice. No significant differences in uterine weight were observed among all OVX dietary subgroups. The Dz subgroup was found to exhibit higher plasma equol and O-desmethylangolensin (O-DMA) concentrations, as well as greater femoral BMD, compared to all other OVX subgroups. Furthermore, when compared to the Dz group, kanamycin intake decreased plasma equol and O-DMA concentrations, as well as femoral BMD in the OVX mice.

Conclusions: These results suggest that kanamycin intake inhibited the conversion of daidzein to equol and O-DMA, blocking the preventive effects of daidzein on bone loss in OVX mice. Therefore, the bone-protective effects of daidzein intake may be predominantly associated with increased plasma concentrations of either equol or O-DMA.

Keywords: Bone mineral density; Daidzein; Equol; Kanamycin; O-desmethylangolensin; Ovariectomy.

MeSH terms

  • Administration, Oral
  • Animals
  • Biotransformation
  • Body Weight / drug effects
  • Bone Density / drug effects*
  • Diet
  • Disease Models, Animal
  • Equol / blood
  • Female
  • Femur / diagnostic imaging
  • Femur / drug effects*
  • Femur / metabolism
  • Humans
  • Isoflavones / administration & dosage*
  • Isoflavones / antagonists & inhibitors
  • Isoflavones / blood
  • Kanamycin / adverse effects*
  • Mice
  • Organ Size / drug effects
  • Osteoporosis / diagnostic imaging
  • Osteoporosis / etiology
  • Osteoporosis / metabolism
  • Osteoporosis / prevention & control*
  • Ovariectomy / adverse effects*
  • Phytoestrogens / administration & dosage*
  • Phytoestrogens / antagonists & inhibitors
  • Phytoestrogens / blood
  • Uterus / drug effects
  • Uterus / metabolism

Substances

  • Isoflavones
  • Phytoestrogens
  • Equol
  • Kanamycin
  • daidzein
  • O-desmethylangolensin