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The degree of bone mineralization is maintained with single intravenous bisphosphonates in aged estrogen-deficient rats and is a strong predictor of bone strength

  • Wei Yao
  • , Zhiqiang Cheng
  • , Kurt J. Koester
  • , Joel W. Ager
  • , Mehdi Balooch
  • , Aaron Pham
  • , Solomon Chefo
  • , Cheryl Busse
  • , Robert O. Ritchie
  • , Nancy E. Lane*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

The treatment of osteoporotic women with bisphosphonates significantly reduces the incidence of bone fractures to a degree greater than can be explained by an increase in bone mineral density. In this study, 18-month Fischer 344 rats were ovariectomized and treated with a single dose of risedronate (intravenous, iv, 500 μg), zoledronic acid (iv, 100 μg) or continuous raloxifene (2 mg/kg, po, 3×/week). High resolution microCT was used to measure lumbar vertebral bone microarchitecture, the degree of bone mineralization (DBM) and the distribution of mineral. Small angle X-ray scattering was used to investigate mineral crystallinity. We found prolonged estrogen deficiency, reduced trabecular bone volume, and increased micro architecture bone compression strength lowered the degree of mineralization. Treatment with resorptive agents (bisphosphonates > raloxifene) prevented the loss of mineralization, trabecular bone volume and bone compression strength. Crystal size was not changed with OVX or with anti-resorptive treatments. In conclusion, in the aged estrogen-deficient rat model, single intravenous doses of two bisphosphonates were effective in maintaining the compressive bone strength for 180 days by reducing bone turnover, and maintaining the DBM to a greater degree than with raloxifene.
Original languageEnglish
Pages (from-to)804-812
JournalBone
Volume41
Issue number5
Online published10 Jul 2007
DOIs
Publication statusPublished - Nov 2007
Externally publishedYes

Research Keywords

  • Bone mineralization
  • Compression strength
  • Intravenous bisphosphonates
  • OVX
  • Rat

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