Literature DB >> 8266826

A new bisphosphonate, BM 21.0955, prevents bone loss associated with cessation of ovarian function in experimental dogs.

M C Monier-Faugere1, R M Friedler, F Bauss, H H Malluche.   

Abstract

We previously found that bone loss occurs as soon as 1 month after ovariohysterectomy (OHX) in beagle dogs. Indirect evidence pointed to an early dramatic increase in bone resorption. To verify this hypothesis and evaluate the effects of a newly developed bisphosphonate, BM 21.0955 (Boehringer Mannheim), 36 beagle dogs were subjected to OHX and 12 dogs were sham operated (Sham). OHX dogs were divided into six groups (n = 6 each) and received subcutaneous injections of vehicle or BM 21.0955 at various doses (0.1, 0.3, 1, 10, and 100 micrograms/kg/day) for 1 month. Sham dogs were given vehicle (n = 6) or BM 21.0955 (1 microgram/kg/day, n = 6). Iliac crest biopsies and blood drawings were done at baseline and at month 1. OHX dogs given vehicle exhibited a decrease in cancellous bone volume associated with an increase in erosion depth and a decrease in serum levels of 1,25-dihydroxyvitamin D. BM 21.0955 prevented the bone loss at a dose > or = 1 microgram/kg and the increase in erosion depth and the decrease in serum levels of 1,25-(OH)2D at a dose > or = 0.3 microgram/kg. No osteomalacia was observed at any dose of BM 21.0955. Bone turnover was reduced only when BM 21.0955 was administered at doses of 10 or 100 micrograms/kg. There were no changes in body weight or serum levels of calcium, phosphorus, creatinine, parathyroid hormone, or osteocalcin in all groups. The increase in erosion depth in OHX dogs given vehicle proves that the early rapid bone loss after cessation of ovarian function is related to an increase in osteoclastic activity. The antiosteoclastic activity of BM 21.0955 at a dose > or = 1 microgram/kg prevents this increase and preserves bone volume. The absence of any signs of osteomalacia at any dose confers a relatively wide therapeutic margin to BM 21.0955. BM 21.0955 at a dose > or = 10 micrograms/kg also acts as an inhibitor of bone turnover. This is not observed at a dose of 1 microgram/kg, at least after 1 month of administration.

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Year:  1993        PMID: 8266826     DOI: 10.1002/jbmr.5650081109

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  10 in total

Review 1.  Bone biopsy in patients with osteoporosis.

Authors:  Hartmut H Malluche; Hanna Mawad; Marie-Claude Monier-Faugere
Journal:  Curr Osteoporos Rep       Date:  2007-12       Impact factor: 5.096

Review 2.  Treating osteoporosis with bisphosphonates and addressing adherence: a review of oral ibandronate.

Authors:  Charles H Chesnut
Journal:  Drugs       Date:  2006       Impact factor: 9.546

3.  The bisphosphonate ibandronate, given daily as well as discontinuously, decreases bone resorption and increases calcium retention as assessed by 45Ca kinetics in the intact rat.

Authors:  H Fleisch
Journal:  Osteoporos Int       Date:  1996       Impact factor: 4.507

Review 4.  Ibandronate in osteoporosis: preclinical data and rationale for intermittent dosing.

Authors:  Frieder Bauss; R Graham G Russell
Journal:  Osteoporos Int       Date:  2004-03-26       Impact factor: 4.507

5.  Anti-resorptive agents reduce the size of resorption cavities: a three-dimensional dynamic bone histomorphometry study.

Authors:  J B Matheny; C R Slyfield; E V Tkachenko; I Lin; K M Ehlert; R E Tomlinson; D L Wilson; C J Hernandez
Journal:  Bone       Date:  2013-08-26       Impact factor: 4.398

Review 6.  Review of nonprimate, large animal models for osteoporosis research.

Authors:  Susan Reinwald; David Burr
Journal:  J Bone Miner Res       Date:  2008-09       Impact factor: 6.741

Review 7.  Ibandronate treatment for osteoporosis: rationale, preclinical, and clinical development of extended dosing regimens.

Authors:  Solomon Epstein
Journal:  Curr Osteoporos Rep       Date:  2006-03       Impact factor: 5.096

8.  Lifelong administration of high doses of ibandronate increases bone mass and maintains bone quality of lumbar vertebrae in rats.

Authors:  S Lalla; L A Hothorn; N Haag; R Bader; F Bauss
Journal:  Osteoporos Int       Date:  1998       Impact factor: 4.507

Review 9.  A new concept for bisphosphonate therapy: a rationale for the development of monthly oral dosing of ibandronate.

Authors:  Jean-Yves Reginster; Dieter Felsenberg; Cyrus Cooper; Jacob A Stakkestad; Paul D Miller; David L Kendler; Silvano Adami; Michael R McClung; Michael A Bolognese; Roberto Civitelli; Etienne Dumont; Bernard Bonvoisin; Robert R Recker; Pierre D Delmas
Journal:  Osteoporos Int       Date:  2005-06-14       Impact factor: 4.507

10.  Ibandronate: the first once-monthly oral bisphosphonate for treatment of postmenopausal osteoporosis.

Authors:  Frieder Bauss; Ralph C Schimmer
Journal:  Ther Clin Risk Manag       Date:  2006-03       Impact factor: 2.423

  10 in total

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