A Longitudinal Study of the Effect of Genistein on Bone in Two Different Murine Models of Diminished Estrogen-Producing Capacity
Author(s) -
Susan Reinwald,
Loretta P. Mayer,
Patricia B. Hoyer,
Charles H. Turner,
Stephen Barnes,
Connie M. Weaver
Publication year - 2009
Publication title -
journal of osteoporosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.421
H-Index - 19
eISSN - 2090-8059
pISSN - 2042-0064
DOI - 10.4061/2010/145170
Subject(s) - ovariectomized rat , genistein , estrous cycle , medicine , ovary , endocrinology , estrogen , in vivo , biology , microbiology and biotechnology
This experiment was designed to assess the capacity of dietary genistein (GEN), to attenuate bone loss in ovariectomized (OVX) and ovary-intact VCD-treated mice. Pretreatment of mice with 4-vinylcyclohexene diepoxide (VCD) gradually and selectively destroys ovarian follicles whilst leaving ovarian androgen-producing cells largely intact. VCD induces a perimenopause-like condition prior to the onset of reproductive acyclicity. Sixteen-week-old C57BL/6J mice were randomized to five treatment groups: sham(SHM), OVX, SHM + VCD, OVX + GEN, and SHM + VCD + GEN. In vivo, blood samples were drawn for hormone and isoflavone analyses, estrous cycles were monitored, and X-ray imaging was performed to assess changes in bone parameters. Following sacrifice, ovaries were assessed histologically, bone microarchitecture was evaluated via microcomputed tomography, and bone mechanical properties were measured. Some effects of GEN were observed in OVX mice, but GEN effects were not able to be evaluated in VCD-treated mice due to the subtle diminution of bone during the 4 months of this experiment.
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